Scedosporium apiospermum: changing clinical spectrum of a therapy-refractory opportunist

References

• Cimon B, Carrere J, Chazalette JP, et al. Fungal colonization and immune response to fungi in cystic fibrosis. J Mycol Méd 1995; 5: 53–56
   Web of Science ®Google Scholar
• Maertens JA, Boogaerts MA. Antifungal prophylaxis in neutropenia. Curr Opin Infect Dis 1999; 12: 549–555
   PubMedGoogle Scholar
• Nucci M. Emerging moulds: Fusarium, Scedosporium and Zygomycetes in transplant recipients. Curr Opin Infect Dis 2003; 16: 607–612
   PubMed Web of Science ®Google Scholar
• Pagano L, Girmenia C, Mele L, et al. Infections caused by filamentous fungi in patients with hematologic malignancies. A report of 391 cases by GIMEMA Infection Program. Haematologica 2001; 86: 862–870
   PubMed Web of Science ®Google Scholar
• Kleinschmidt-DeMasters BK. Central nervous system aspergillosis: a 20-year retrospective series. Hum Pathol 2002; 33: 116–124
   PubMed Web of Science ®Google Scholar
• Lopez FA, Crowley RS, Wastila L, Valantine HA, Remington JS. Scedosporium apiospermum (Pseudallescheria boydii) infection in a heart transplant recipient: a case of mistaken identity. J Heart Lung Transpl 1998; 17: 321–324
   PubMed Web of Science ®Google Scholar
• Guarro J, Gené J. Acrophialophora fusispora misidentified as Scedosporium prolificans. J Clin Microbiol 2002; 40: 3544
   PubMedGoogle Scholar
• Castiglioni B, Sutton DA, Rinaldi MG, Fung J, Kusne S. Pseudallescheria boydii (anamorph Scedosporium apiospermum). Infection in solid organ transplant recipients in a tertiary medical center and review of the literature. Medicine (Baltimore) 2002; 81: 333–348
   PubMed Web of Science ®Google Scholar
• Husain S, Muñoz P, Forrest G, et al. Infections due to Scedosporium apiospermum and Scedosporium prolificans in transplant recipients: clinical characteristics and impact of antifungal agent therapy on outcome. Clin Infect Dis 2005; 40: 89–99
   PubMed Web of Science ®Google Scholar
• Nesky MA, McDougal EC, Peacock JE., Jr. Pseudallescheria boydii brain abscess successfully treated with voriconazole and surgical drainage: case report and literature review of central nervous system pseudallescheriasis. Clin Infect Dis 2000; 31: 673–677
   PubMed Web of Science ®Google Scholar
• Steinbach WJ, Perfect JR. Scedosporium species infections and treatments. J Chemother 2003; 15(Suppl 2)16–27
   PubMed Web of Science ®Google Scholar
• Walsh TJ, Groll A, Hiemenz J, et al. Infections due to emerging and uncommon medically important fungal pathogens. Clin Microbiol Infect 2004; 10(Suppl 1)48–66
   PubMed Web of Science ®Google Scholar
• Kimura M, McGinnis MR. Fontana-Masson-stained tissue from culture-proven mycoses. Arch Pathol Lab Med 1998; 122: 1107–1111
   PubMedGoogle Scholar
• Shear CL. Life history of an undescribed ascomycete isolated from a granular mycetoma of man. Mycologia 1922; 14: 239–243
   Google Scholar
• de Hoog GS, Guarro J, Gené J, Figueras MJ. Atlas of Clinical Fungi2nd edn. Centraalbureau voor Schimmelcultures/Reus: Universitat Rovira i Virgili, Utrecht 2000
   Google Scholar
• Dykstra MJ, Salkin IF, McGinnis MR. An ultrastructural comparison of conidiogenesis in Scedosporium apiospermum, Scedosporium inflatum and Scopulariopsis brumptii. Mycologia 1989; 81: 896–904
   Web of Science ®Google Scholar
• Hironaga M, Watanabe S. Annellated conidiogenous cells in Petriellidium boydii (Scedosporium apiospermum). Sabouraudia 1980; 18: 261–268
   PubMedGoogle Scholar
• Campbell CK, Smith MD. Conidiogenesis in Petriellidium boydii (Pseudallescheria boydii). A light and electron microscope study. Mycopathologia 1982; 78: 145–150
   PubMed Web of Science ®Google Scholar
• Campbell CK. Polycytella hominis gen. et sp. nov., a cause of human pale grain mycetoma. J Med Vet Mycol 1987; 25: 301–305
   PubMedGoogle Scholar
• Borman AM, Campbell CK, Linton CJ, Johnson EM. Polycytella hominis is a mutated form of Scedosporium apiospermum, as shown by gene sequence analysis. Med Mycol 2005; 44: 33–39
   Google Scholar
• Berbee ML, Taylor JW. Convergence in ascospore discharge mechanism among pyrenomycete fungi based on 18S ribosomal RNA gene sequence. Mol Phylogenet Evol 1992; 1: 59–71
   PubMed Web of Science ®Google Scholar
• Barron GL, Cain RF, Gilman JC. A revision of the genus Petriella. Can J Bot 1961; 39: 837–845
   Google Scholar
• Udagawa SI. Microascaceae in Japan. J Gen Appl Microbiol 1963; 9: 137–148
   Google Scholar
• von Arx JA. Ostiolate and nonostiolate Pyrenomycetes. Proc K Ned Akad Wet 1973; 76: 289–296
   Google Scholar
• Issakainen J, Jalava J, Eerola E, Campbell CK. Relatedness of Pseudallescheria, Scedosporium and Graphium pro parte based on SSU rDNA sequences. J Med Vet Mycol 1997; 35: 389–398
   PubMedGoogle Scholar
• Issakainen J, Jalava J, Saari J, Campbell CK. Relationship of Scedosporium prolificans with Petriella confirmed by partial LSU rDNA sequences. Mycol Res 1999; 103: 1179–1184
   Web of Science ®Google Scholar
• Okada G, Seifert KA, Takematsu A, et al. A molecular phylogenetic reappraisal of the Graphium complex based on 18S rDNA sequences. Can J Bot 1988; 76: 1495–1506
   Google Scholar
• Rainer J, de Hoog GS, Wedde M, Gräser Y, Gilges S. Molecular variability of Pseudallescheria boydii, a neurotropic opportunist. J Clin Microbiol 2000; 38: 3267–3273
   PubMed Web of Science ®Google Scholar
• Gilgado F, Cano J, Gené J, Guarro J. Molecular phylogeny of the Pseudallescheria boydii species complex. Proposal of two new species. J Clin Microbiol 2005; 43: 4930–4942
   PubMed Web of Science ®Google Scholar
• Guého E, de Hoog GS. Taxonomy of the medical species of Pseudallescheria and Scedosporium. J Mycol Méd 1991; 118: 3–9
   Google Scholar
• Rainer J, de Hoog GS. Molecular taxonomy and ecology of Pseudallescheria, Petriella and Scedosporium prolificans (Microascaceae) containing opportunistic agents on humans. Mycol Res 2006; 110: 151–160
   PubMed Web of Science ®Google Scholar
• Ajello L. The isolation of Allescheria boydii Shear, an etiologic agent of mycetomas, from soil. J Trop Med 1952; 1: 227–238
   Google Scholar
• Kurup PV, Schmitt JA. Human-pathogenic fungi in the soils of Ohio. Ohio J Sci 1970; 70: 291–295
   Google Scholar
• Sotgiu G, Mazzoni A, Mantovani A, Ajello L, Palmer L. Survey of soil for human pathogenic fungi from Emilia Romagna, region of Italy. Isolation of Allescheria boydii, Cryptococcus neoformans, and Histoplasma capsulatum. Am J Epidemiol 1966; 83: 329–337
   PubMed Web of Science ®Google Scholar
• Bakerspigel A, Schaus D. Petriellidosis (pseudallescheriasis) in southwestern Ontario, Canada. Sabouraudia 1984; 22: 247–249
   PubMedGoogle Scholar
• Bell RG. The development in beef cattle manure of Petriellidium boydii (Shear) Malloch, a potential pathogen for man and cattle. Can J Microbiol 1976; 22: 552–556
   PubMed Web of Science ®Google Scholar
• Bell RG. Comparative virulence and immunodiffusion analysis of Petriellidium boydii (Shear) Malloch strains isolated from feedlot manure and a human mycetoma. Can J Microbiol 1978; 24: 856–863
   PubMedGoogle Scholar
• Cooke WB, Kahler PG. Isolation of potentially pathogenic fungi from polluted water and sewage. Publ Health Rep 1955; 170: 689–694
   Google Scholar
• de Hoog GS, Marvin-Sikkema FD, Lahpoor GA, et al. Ecology and physiology of the emerging opportunistic fungi Pseudallescheria boydii and Scedosporium prolificans. Mycoses 1994; 37: 71–78
   PubMed Web of Science ®Google Scholar
• Fisher JF, Shadomy S, Teabeaut JR, et al. Near-drowning complicated by brain abscess due to Petriellidium boydii. Arch Neurol 1982; 39: 511–513
   PubMedGoogle Scholar
• Llanos C, Kjoller A. Changes in the flora of soil fungi following waste application. Oikos 1976; 27: 377–382
   Web of Science ®Google Scholar
• Davies JS, Wellman A, Zajic JE. Hyphomycetes utilizing natural gas. Can J Microbiol 1973; 19: 81–85
   PubMed Web of Science ®Google Scholar
• Zajic JE, Volesky B, Wellman A. Growth of Graphium sp. on natural gas. Can J Microbiol 1969; 15: 1231–1236
   PubMedGoogle Scholar
• García-Peña EI, Hernández S, Favela-Torres E, Auria R, Revah S. Toluene biofiltration by the fungus Scedosporium apiospermum TB1. Biotechnol Bioeng 2001; 76: 61–69
   PubMed Web of Science ®Google Scholar
• April TM, Abbott SP, Foght JM, Currah RS. Degradation of hydrocarbons in crude oil by the ascomycete Pseudallescheria boydii (Microascaceae). Can J Microbiol 1998; 44: 270–278
   PubMed Web of Science ®Google Scholar
• Ajello L, Kuttin ES, Beemer AM, Kaplan W, Padhye A. Occurrence of Histoplasma capsulatum Darling, 1906 in Israel, with a review of the current status of histoplasmosis in the Middle East. Am J Trop Med Hyg 26; 1977: 140–147
   Google Scholar
• Vissiennon T. Untersuchungen zur Pilzbelastung im Hühnerstall und ihre ätiopathogenetische Bedeutung für Mensch und Tier [Fungal flora in chicken stalls and its etiopathogenic importance for humans and animals]. Berl Münch Tierarztl Wochenschr 1999; 112: 104–107
   PubMedGoogle Scholar
• Brandsberg JW, Weeks RJ, Hill WB, Piggott WR. A study of fungi found in association with Histoplasma capsulatum: three bird roosts in S. E. Missouri, U.S.A. Mycopathol Mycol Appl 1969; 38: 71–81
   PubMedGoogle Scholar
• Kirk PW. A comparison of saline tolerance and sporulation in marine and clinical isolates of Allescheria boydii Shear. Mycopathol Mycol Appl 1967; 33: 65–75
   Google Scholar
• Dabrowa N, Landau JW, Newcomer VD, Plunkett OA. A survey of tide–washed coastal areas of Southern California for fungi potentially pathogenic to man. Mycopathologia 1964; 24: 136–150
   Google Scholar
• Pawar VH, Padhye AA, Thirumalachar MJ. Isolation of Monosporium apiospermum from marine soil in Bombay, Research Laboratories, Hindustan Antibiotics Ltd. Pimpri 1963; 6: 50–53
   Google Scholar
• Aho R, Hirn J. A survey of fungi and some indicator bacteria in chlorinated water of indoor public swimming pools. Zentralbl Bakteriol Mikrobiol Hyg B 1981; 173: 242–249
   PubMedGoogle Scholar
• Summerbell RC. The benomyl test as a fundamental diagnostic method for medical mycology. J Clin Microbiol 1993; 31: 572–577
   PubMed Web of Science ®Google Scholar
• Lingappa BT, Lingappa Y. Isolation of Allescheria boydii Shear from heated Indian soils. Curr Sci 1961; 2: 70–72
   Google Scholar
• Hagari Y, Ishioka S, Ohyama F, Mihara M. Cutaneous infection showing sporotrichoid spread caused by Pseudallescheria boydii (Scedosporium apiospermum): successful detection of fungal DNA in formalin–fixed, paraffin–embedded sections by seminested PCR. Arch Dermatol 2002; 138: 271–272
   PubMedGoogle Scholar
• Wedde M, Muller D, Tintelnot K, de Hoog GS, Stahl U. PCR–based identification of clinically relevant Pseudallescheria/Scedosporium strains. Med Mycol 1998; 36: 61–67
   PubMed Web of Science ®Google Scholar
• Sandhu GS, Kline BC, Stockman L, Roberts GD. Molecular probes for diagnosis of fungal infections. J Clin Microbiol 1995; 33: 2913–2919
   PubMed Web of Science ®Google Scholar
• Willinger B, Obradovic A, Selitsch B, et al. Detection and identification of fungi from fungus balls of the maxillary sinus by molecular techniques. J Clin Microbiol 2003; 41: 581–585
   PubMed Web of Science ®Google Scholar
• Zouhair R, Defontaine A, Ollivier C, et al. Typing of Scedosporium apiospermum by multilocus enzyme electrophoresis and random amplification of polymorphic DNA. J Med Microbiol 2001; 50: 925–932
   PubMed Web of Science ®Google Scholar
• Defontaine A, Zouhair R, Cimon B, et al. Genotyping study of Scedosporium apiospermum isolates from patients with cystic fibrosis. J Clin Microbiol 2002; 40: 2108–2114
   PubMed Web of Science ®Google Scholar
• Rüchel R, Margraf S. Rapid microscopical diagnosis of deep-seated mycoses following maceration of fresh specimens and staining with optical brighteners. Mycoses 1993; 36: 239–242
   PubMedGoogle Scholar
• Rüchel R, Schaffrinski M, Seshan KR, Cole GT. Vital staining of fungal elements in deep–seated mycotic lesions during experimental murine mycoses using the parenterally applied optical brightener Blankophor. Med Mycol 2000; 38: 231–237
   PubMed Web of Science ®Google Scholar
• Kaufman L, Standard PG, Jalbert M, Kraft DE. Immunohistologic identification of Aspergillus spp. and other hyaline fungi by using polyclonal fluorescent antibodies. J Clin Microbiol 1997; 35: 2206–2209
   PubMed Web of Science ®Google Scholar
• Rippon JW. Medical Mycology. The Pathogenic Fungi and the Pathogenic Actinomycetes3rd edn. Saunders, Philadelphia 1998
   Google Scholar
• Hay RJ, McKenzie DWR. The histopathological features of pale grain eumycetoma. Trans R Soc Trop Med Hyg 1982; 76: 839–844
   PubMedGoogle Scholar
• Salkin IF, McGinnis MR, Dykstra MJ, Rinaldi MG. Scedosporium inflatum, an emerging pathogen. J Clin Microbiol 1988; 26: 498–503
   PubMed Web of Science ®Google Scholar
• Dixon DM, Polak–Wyss A. The medically important dematiaceous fungi and their identification. Mycoses 1991; 34: 1–18
   PubMed Web of Science ®Google Scholar
• Albernaz V, Huston B, Castillo M, Mukherji S, Bouldin TW. Pseudallescheria boydii infection of the brain: imaging with pathologic confirmation. Am J Neuroradiol 1996; 17: 589–592
   PubMedGoogle Scholar
• Dubeau F, Roy LE, Allard J, et al. Brain abscess due to Petriellidium boydii. Can J Neurol Sci 1984; 11: 395–398
   PubMedGoogle Scholar
• Shih LY, Lee N. Disseminated petriellidiosis (allescheriasis) in a patient with refractory acute lymphoblastic leukaemia. J Clin Pathol 1984; 37: 78–82
   PubMed Web of Science ®Google Scholar
• Yoo D, Lee WH, Kwon–Chung KJ. Brain abscesses due to Pseudallescheria boydii associated with primary non–Hodgkin's lymphoma of the central nervous system: a case report and literature review. Rev Infect Dis 1985; 7: 272–277
   PubMedGoogle Scholar
• Berenguer J, Díaz–Mediavilla J, Urra D, Muñoz P. Central nervous system infection caused by Pseudallescheria boydii: case report and review. Rev Infect Dis 1989; 11: 890–896
   PubMedGoogle Scholar
• Hachimi–Idrissi S, Willemsen M, Desprechins B, et al. Pseudallescheria boydii and brain abscesses. Pediatr Infect Dis J 1990; 9: 737–741
   PubMedGoogle Scholar
• Schiess RJ, Coscia MF, McClellan GA. Petriellidium boydii pachymeningitis treated with miconazole and ketoconazole. Neurosurgery 1984; 14: 220–224
   PubMedGoogle Scholar
• Anderson RL, Carroll TF, Harvey JT, Myers MG. Petriellidium (Allescheria) boydii orbital and brain abscess treated with intravenous miconazole. Am J Ophthalmol 1984; 97: 771–775
   PubMedGoogle Scholar
• Baudrillard JC, Rousseaux P, Lerais JM, et al. Anéurysmes mycotiques fongiques et abcès cérébraux multiples à Scedosporium apiospermum. À propos d'une observation avec revue de la littérature [Fungal aneurysms and multiple cerebral abscesses due to Scedosporium apiospermum. About a case with a review of the literature]. J Radiol 1985; 66: 321–326
   PubMedGoogle Scholar
• Durieu I, Parent M, Ajana F, et al. Monosporium apiospermum meningoencephalitis: a clinico–pathological case. J Neurol Neurosurg Psychiatry 1991; 54: 731–733
   PubMedGoogle Scholar
• Gari M, Fruit J, Rousseaux P, et al. Scedosporium (Monosporium) apiospermum: multiple brain abscesses. Sabouraudia 1985; 23: 371–376
   PubMedGoogle Scholar
• Alsip SG, Cobbs CG. Pseudallescheria boydii infection of the central nervous system in a cardiac transplant recipient. South Med J 1986; 79: 383–384
   PubMedGoogle Scholar
• Kershaw P, Freeman R, Templeton D, et al. Pseudallescheria boydii infection of the central nervous system. Arch Neurol 1990; 47: 468–472
   PubMedGoogle Scholar
• Liu K, Howell DN, Perfect JR, Schell WA. Morphologic criteria for the preliminary identification of Fusarium, Paecilomyces, and Acremonium species by histopathology. Am J Clin Pathol 1998; 109: 45–54
   PubMed Web of Science ®Google Scholar
• Walts AE. Pseudallescheria: an underdiagnosed fungus?. Diagn Cytopathol 2001; 25: 153–157
   PubMed Web of Science ®Google Scholar
• Fessler RG, Brown FD. Superior sagittal sinus infection with Petriellidium boydii: case report. Neurosurgery 1989; 24: 604–607
   PubMed Web of Science ®Google Scholar
• Pérez RE, Smith M, McClendon J, Kim J, Eugenio N. Pseudallescheria boydii brain abscess. Complication of an intravenous catheter. Am J Med 1988; 84: 359–362
   PubMedGoogle Scholar
• Hayden RT, Isotalo PA, Parrett T, et al. In situ hybridization for the differentiation of Aspergillus, Fusarium, and Pseudallescheria species in tissue section. Diagn Mol Pathol 2003; 12: 21–26
   PubMed Web of Science ®Google Scholar
• Poza G, Montoya J, Redondo C, et al. Meningitis caused by Pseudallescheria boydii treated with voriconazole. Clin Infect Dis 2000; 30: 981–982
   PubMed Web of Science ®Google Scholar
• Rüchel R, Wilichowski E. Cerebral Pseudallescheria mycosis after near-drowning. Mycoses 1995; 38: 473–475
   PubMed Web of Science ®Google Scholar
• Watanabe S, Hironaga M. An atypical isolate of Scedosporium apiospermum from a purulent meningitis in man. Sabouraudia 1981; 19: 209–215
   PubMedGoogle Scholar
• Nenoff P, Gutz U, Tintelnot K, et al. Disseminated mycosis due to Scedosporium prolificans in an AIDS patient with Burkitt lymphoma. Mycoses 1996; 39: 461–465
   PubMedGoogle Scholar
• Al Refai M, Duhamel C, Le Rochais JP, Icard P. Lung scedosporiosis: a differential diagnosis of aspergillosis. Eur J Cardiothorac Surg 2002; 21: 938–939
   PubMed Web of Science ®Google Scholar
• Chaudhary BA, McAlexander D, el Gammal T, Speir WA. Multiple mycetomas due to Pseudallescheria boydii. South Med J 1987; 80: 653–654
   PubMedGoogle Scholar
• García–Arata MI, Otero MJ, Zomeno M, et al. Scedosporium apiospermum pneumonia after autologous bone marrow transplantation. Eur J Clin Microbiol Infect Dis 1996; 15: 600–603
   PubMedGoogle Scholar
• Marco de Lucas E, Sadaba P, Lastra Garcia-Baron P, et al. Cerebral scedosporiosis: an emerging fungal infection in severe neutropenic patients: CT features and CT pathologic correlation. Eur Radiol 2006; 16: 496–502
   PubMed Web of Science ®Google Scholar
• Lupan DM, Cazin J., Jr. Serological diagnosis of petriellidiosis (allescheriosis). II. Indirect (passive) hemagglutination assay for antibody to polysaccharide antigens of Petriellidium (Allescheria) boydii and Monosporium apiospermum. Mycopathologia 1977; 62: 87–95
   PubMedGoogle Scholar
• Lupan DM, Cazin J., Jr. Humoral response to experimental petriellidiosis. Infect Immun 1979; 24: 843–850
   PubMedGoogle Scholar
• Jabado N, Casanova JL, Haddad E, et al. Invasive pulmonary infection due to Scedosporium apiospermum in two children with chronic granulomatous disease. Clin Infect Dis 1998; 27: 1437–1441
   PubMed Web of Science ®Google Scholar
• McCarthy DS, Longbottom JL, Riddell RW, Batten JC. Pulmonary mycetoma due to Allescheria boydii. Am Rev Respir Dis 1969; 100: 213–216
   PubMedGoogle Scholar
• Pinto MR, Mulloy B, Haido RM, Travassos LR, Barreto Bergter E. A peptidorhamnomannan from the mycelium of Pseudallescheria boydii is a potential diagnostic antigen of this emerging human pathogen. Microbiology 2001; 147: 1499–1506
   PubMed Web of Science ®Google Scholar
• Cimon B, Carrere J, Vinatier JF, et al. Clinical significance of Scedosporium apiospermum in patients with cystic fibrosis. Eur J Clin Microbiol Infect Dis 2000; 19: 53–56
   PubMed Web of Science ®Google Scholar
• Gil–Lamaignere C, Roilides E, Lyman CA, et al. Human phagocytic cell responses to Scedosporium apiospermum (Pseudallescheria boydii): variable susceptibility to oxidative injury. Infect Immun 2003; 71: 6472–6478
   PubMed Web of Science ®Google Scholar
• Gil-Lamaignere C, Winn RM, Simitsopoulou M, et al. Interferon gamma and granulocyte-macrophage colony-stimulating factor augment the antifungal activity of human polymorphonuclear leukocytes against Scedosporium spp.: comparison with Aspergillus spp. Med Mycol 2005; 43: 253–260
   PubMed Web of Science ®Google Scholar
• Gil–Lamaignere C, Roilides E, Mosquera J, Maloukou A, Walsh TJ. Antifungal triazoles and polymorphonuclear leukocytes synergize to cause increased hyphal damage to Scedosporium prolificans and Scedosporium apiospermum. Antimicrob Agents Chemother 2002; 46: 2234–2237
   PubMed Web of Science ®Google Scholar
• Gil-Lamaignere C, Roilides E, Maloukou A, et al. Amphotericin B lipid complex exerts additive antifungal activity in combination with polymorphonuclear leucocytes against Scedosporium prolificans and Scedosporium apiospermum. J Antimicrob Chemother 2002; 50: 1027–1030
   PubMed Web of Science ®Google Scholar
• Winn RM, Gil-Lamaignere C, Roilides E, et al. Effects of interleukin-15 on antifungal responses of human polymorphonuclear leukocytes against Fusarium spp. and Scedosporium spp. Cytokine 2005; 31: 1–8
   PubMedGoogle Scholar
• Carrillo AJ, Guarro J. In vitro activities of four novel triazoles against Scedosporium spp. Antimicrob Agents Chemother 2001; 45: 2151–2153
   PubMed Web of Science ®Google Scholar
• Cuenca-Estrella M, Ruiz-Diez B, Martinez-Suarez JV, Monzon A, Rodriguez-Tudela JL. Comparative in-vitro activity of voriconazole (UK-109,496) and six other antifungal agents against clinical isolates of Scedosporium prolificans and Scedosporium apiospermum. J Antimicrob Chemother 1999; 43: 149–151
   PubMed Web of Science ®Google Scholar
• Del Poeta M, Schell WA, Perfect JR. In vitro antifungal activity of pneumocandin L–743,872 against a variety of clinically important molds. Antimicrob Agents Chemother 1997; 41: 1835–1836
   PubMed Web of Science ®Google Scholar
• Espinel-Ingroff A. Comparison of in vitro activities of the new triazole SCH56592 and the echinocandins MK-0991 (L-743,872) and LY303366 against opportunistic filamentous and dimorphic fungi and yeasts. J Clin Microbiol 1998; 36: 2950–2956
   PubMed Web of Science ®Google Scholar
• Espinel-Ingroff A. In vitro activity of the new triazole voriconazole (UK-109,496) against opportunistic filamentous and dimorphic fungi and common and emerging yeast pathogens. J Clin Microbiol 1998; 36: 198–202
   PubMed Web of Science ®Google Scholar
• Johnson EM, Szekely A, Warnock DW. In-vitro activity of voriconazole, itraconazole and amphotericin B against filamentous fungi. J Antimicrob Chemother 1998; 42: 741–745
   PubMed Web of Science ®Google Scholar
• McGinnis MR, Pasarell L, Sutton DA, et al. In vitro activity of voriconazole against selected fungi. Med Mycol 1998; 36: 239–242
   PubMed Web of Science ®Google Scholar
• Meletiadis J, Meis JF, Mouton JW, et al. In vitro activities of new and conventional antifungal agents against clinical Scedosporium isolates. Antimicrob Agents Chemother 2002; 46: 62–68
   PubMed Web of Science ®Google Scholar
• Minassian B, Huczko E, Washo T, Bonner D, Fung-Tomc J. In vitro activity of ravuconazole against Zygomycetes, Scedosporium and Fusarium isolates. Clin Microbiol Infect 2003; 9: 1250–1252
   PubMed Web of Science ®Google Scholar
• Odabasi Z, Paetznick VL, Rodriguez JR, Chen E, Ostrosky-Zeichner L. In vitro activity of anidulafungin against selected clinically important mold isolates. Antimicrob Agents Chemother 2004; 48: 1912–1915
   PubMed Web of Science ®Google Scholar
• Pfaller MA, Marco F, Messer SA, Jones RN. In vitro activity of two echinocandin derivatives, LY303366 and MK-0991 (L-743,792), against clinical isolates of Aspergillus, Fusarium, Rhizopus, and other filamentous fungi. Diagn Microbiol Infect Dis 1998; 30: 251–255
   PubMed Web of Science ®Google Scholar
• Radford SA, Johnson EM, Warnock DW. In vitro studies of activity of voriconazole (UK-109,496), a new triazole antifungal agent, against emerging and less–common mold pathogens. Antimicrob Agents Chemother 1997; 41: 841–843
   PubMed Web of Science ®Google Scholar
• Hennequin C. Epidémiologie des mycoses invasives. L'expérience d'une centre hospitalo–universitaire parisien. Rev Méd Interne 1996; 17: 754–760
   PubMedGoogle Scholar
• Uchida K, Nishiyama Y, Yokota N, Yamaguchi H. In vitro antifungal activity of a novel lipopeptide antifungal agent, FK463, against various fungal pathogens. J Antibiot (Tokyo) 2000; 53: 1175–1181
   PubMed Web of Science ®Google Scholar
• Walsh TJ, Peter J, McGough DA, et al. Activities of amphotericin B and antifungal azoles alone and in combination against Pseudallescheria boydii. Antimicrob Agents Chemother 1995; 39: 1361–1364
   PubMed Web of Science ®Google Scholar
• González GM, Fothergill AW, Sutton DA, Rinaldi MG, Loebenberg D. In vitro activities of new and established triazoles against opportunistic filamentous and dimorphic fungi. Med Mycol 2005; 43: 281–284
   PubMed Web of Science ®Google Scholar
• Steinbach WJ, Schell WA, Miller JL, Perfect JR. Scedosporium prolificans osteomyelitis in an immunocompetent child treated with voriconazole and caspofungin, as well as locally applied polyhexamethylene biguanide. J Clin Microbiol 2003; 41: 3981–3985
   PubMed Web of Science ®Google Scholar
• Cunningham R, Mitchell DC. Amphotericin B responsive Scedosporium apiospermum infection in a patient with acute myeloid leukaemia. J Clin Pathol 1996; 49: 93–94
   PubMed Web of Science ®Google Scholar
• Johnson MD, MacDougall C, Ostrosky–Zeichner L, Perfect JR, Rex JH. Combination antifungal therapy. Antimicrob Agents Chemother 2004; 48: 693–715
   PubMed Web of Science ®Google Scholar
• Li RK, Rinaldi MG. In vitro antifungal activity of nikkomycin Z in combination with fluconazole or itraconazole. Antimicrob Agents Chemother 1999; 43: 1401–1405
   PubMed Web of Science ®Google Scholar
• Yustes C, Guarro J. In vitro synergistic interaction between amphotericin B and micafungin against Scedosporium spp. Antimicrob Agents Chemother 2005; 49: 3498–3500
   PubMedGoogle Scholar
• Fienberg R. Madura foot in a native American. Am J Clin Pathol 1944; 14: 239–246
   Google Scholar
• Gay DM, Bigelow JB. Madura foot due to Monosporium apiospermum in a native American. Am J Pathol 1930; 6: 325–335
   PubMedGoogle Scholar
• Reyes AC. A contribution to the study of mycetoma in The Philippines: maduromycosis caused by Monosporium apiospermum (laboratory studies). Acta Med Philipp 1963; 19: 89–102
   PubMedGoogle Scholar
• Schmitt JA, Zabransky RJ, Janidlo AS, Parsons JE. Experimental maduromycosis in the laboratory mouse. Mycopathologia 1962; 18: 164–168
   Google Scholar
• Lupan DM, Cazin J., Jr. Pathogenicity of Allescheria boydii for mice. Infect Immun 1973; 8: 743–751
   PubMedGoogle Scholar
• Jones JW, Alden HS. Maduromycotic mycetoma (Madura foot): report of a case occurring in an American negro. J Am Med Assoc 1931; 96: 256–260
   Google Scholar
• Benham RW. Allescheria boydii, causative agent in a case of meningitis. J Invest Dermatol 1948; 10: 99–110
   PubMed Web of Science ®Google Scholar
• Capilla J, Guarro J. Correlation between in vitro susceptibility to voriconazole and in vivo outcome of scedosporiosis in guinea pigs. Antimicrob Agents Chemother 2004; 48: 4009–4011
   PubMedGoogle Scholar
• Capilla J, Mayayo E, Serena C, Javier JF, Guarro J. A novel murine model of cerebral scedosporiosis: lack of efficacy of amphotericin B. J Antimicrob Chemother 2004; 54: 1092–1095
   PubMed Web of Science ®Google Scholar
• Ortoneda M, Pastor FJ, Mayayo E, Guarro J. Comparison of the virulence of Scedosporium prolificans strains from different origins in a murine model. J Med Microbiol 2002; 51: 924–928
   PubMed Web of Science ®Google Scholar
• Gonzalez GM, Tijerina R, Najvar L, et al. Experimental murine model of disseminated Pseudallescheria infection. Med Mycol 2002; 40: 243–248
   PubMedGoogle Scholar
• Capilla J, Serena C, Pastor FJ, Ortoneda M, Guarro J. Efficacy of voriconazole in treatment of systemic scedosporiosis in neutropenic mice. Antimicrob Agents Chemother 2003; 47: 3976–3978
   PubMed Web of Science ®Google Scholar
• Ortoneda M, Capilla J, Pastor FJ, Serena C, Guarro J. Interaction of granulocyte colony–stimulating factor and high doses of liposomal amphotericin B in the treatment of systemic murine scedosporiosis. Diagn Microbiol Infect Dis 2004; 50: 247–251
   PubMed Web of Science ®Google Scholar
• Gonzalez GM, Tijerina R, Najvar LK, et al. Activity of posaconazole against Pseudallescheria boydii: in vitro and in vivo assays. Antimicrob Agents Chemother 2003; 47: 1436–1438
   PubMed Web of Science ®Google Scholar
• Siebenmann F. Die Schimmelmykosen des menschlichen Ohres [The mycoses of the human ear]. J. F. Bergmann, WiesbadenGermany 1899
   Google Scholar
• Saccardo PA. Notae mycologicae [Mycological notes]. Annls Mycol 1911; 9: 249–257
   Google Scholar
• Creitz J, Harris HV. Isolation of Allescheria boydii from sputum. Am Rev Tuberculosis 1955; 71: 126–130
   PubMedGoogle Scholar
• Frágner P, Hejzlar J. ‘Graphiosis’ – eine neue Erkrankung des Menschen? [‘Graphiosis’ – a new human disease?]. Ceská Mykol 1973; 27: 98–106
   Google Scholar
• Zapater RC, Albesi EJ. Corneal monosporiosis. A review and report of 1 case. Ophthalmologica 1979; 178: 147
   Google Scholar
• van Hecke E, Geerts ML, den Dooven D. Petriellidiosis of the skin. Mykosen 1982; 26: 17–21
   Google Scholar
• Sawada M, Isogai S, Miyake S, Kubota T, Yoshizawa Y. Pulmonary pseudallescherioma associated with systemic lupus erythematosus. Intern Med 1998; 37: 1046–1049
   PubMedGoogle Scholar
• Warnock DW, Richardson MD. Fungal Infection in the Compromised Patient. Wiley, Chichester 1991
   Google Scholar
• Severo LC, Oliveira FM, Londero AT. Subcutaneous scedosporiosis. Report of two cases and review of the literature. Rev Inst Med Trop Sao Paulo 1997; 39: 227–230
   PubMedGoogle Scholar
• Odds FC, Arai T, Disalvo AF, et al. Nomenclature of fungal diseases – A report and recommendations from a sub–committee of the International Society for Human and Animal Mycology (ISHAM). J Med Vet Mycol 1992; 30: 1–10
   PubMedGoogle Scholar
• Groves, CRN. The Johns Hopkins Microbiology Newsletter. 16; 1997 [ cited 2004 Jun 22] Available from:< http://pathology5.pathology.jhmi.edu/micro/v16n13.htm>
   Google Scholar
• Yücel A, Köslü A, Numan S. [A case of maduromycosis in hand, caused by Petriellidium boydii]. Cerr Tip Fak Derg 1981; 22: 570–576
   Google Scholar
• Ichikawa T, Saiki M, Tokunaga S, Saida T. Scedosporium apiospermum skin infection in a patient with nephrotic syndrome. Acta Derm Venereol 1997; 77: 172–173
   PubMedGoogle Scholar
• Castro LG, Belda JW, Salebian A, Cuce LC. Mycetoma: a retrospective study of 41 cases seen in Sao Paulo, Brazil, from to 1989. Mycoses ; 36 1978; 1993: 89–95
   Google Scholar
• Venugopal PV, Venugopal TV. Pale grain eumycetomas in Madras. Australas J Dermatol 1995; 36: 149–151
   PubMedGoogle Scholar
• Ahmed J, Ditmars DM, Sheppard T, et al. Recurrence of Scedosporium apiospermum infection following renal re–transplantation. Am J Transplant 2004; 4: 1720–1724
   PubMed Web of Science ®Google Scholar
• Fernandez–Guerrero ML, Ruiz BP, Ales JM. Postcraniotomy mycetoma of the scalp and osteomyelitis due to Pseudallescheria boydii. J Infect Dis 1987; 156: 855
   PubMedGoogle Scholar
• Gener FA, Kustimur S, Sultan N, Sever A. Ueber eine Pilz–induzierte Arthritis durch Scedosporium apiospermum (Pseudallescheria boydii) [About a fungal arthritis due to Scedosporium apiospermum (Pseudallescheria boydii)]. Z Rheumatol 1991; 50: 219–221
   PubMedGoogle Scholar
• Ginter G, de Hoog GS, Pschaid A, et al. Arthritis without grains caused by Pseudallescheria boydii. Mycoses 1995; 38: 369–371
   PubMedGoogle Scholar
• Hayden G, Lapp C, Loda F. Arthritis caused by Monosporium apiospermum treated with intraarticular amphotericin B. Am J Dis Child 1977; 131: 927
   PubMedGoogle Scholar
• Lutwick LI, Rytel MW, Yanez JP, Galgiani JN, Stevens DA. Deep infections from Petriellidium boydii treated with miconazole. JAMA 1979; 241: 272–273
   PubMed Web of Science ®Google Scholar
• Piper JP, Golden J, Brown D, Broestler J. Successful treatment of Scedosporium apiospermum suppurative arthritis with itraconazole. Pediatr Infect Dis J 1990; 9: 674–675
   PubMed Web of Science ®Google Scholar
• Dirschl DR, Henderson RC. Patellar overgrowth after infection of the knee. J Bone Joint Surg 1991; 73A: 940–941
   Google Scholar
• Lavy D, Morin O, Venet G, et al. Pseudallescheria boydii knee arthritis in a young immunocompetent adult two years after a compound patellar fracture. Joint Bone Spine 2001; 68: 517–520
   PubMed Web of Science ®Google Scholar
• Foster MR, Friedenberg ZB, Passero F. Lumbar Petriellidium boydii osteomyelitis with a systemic presentation. J Spinal Disord 1994; 7: 356–360
   PubMedGoogle Scholar
• Hervé F, Drouhet E, Dupont B, Barois A, Beneux J. Ostéoarthrite mycosique du genou avec destruction articulaire traitée par kétoconazole. Arch Fr Pediatr 1983; 40: 309–314
   PubMedGoogle Scholar
• Dellestable F, Kures L, Mainard D, Pere P, Gaucher A. Fungal arthritis due to Pseudallescheria boydii (Scedosporium apiospermum). J Rheumatol 1994; 21: 766–768
   PubMedGoogle Scholar
• Le Gouill SL, Morineau N, Miegeville M, et al. Ostéoarthrite à Pseudallescheria boydii chez un patient porteur de leucémie aigué lymphoblastique: à propos d'un cas. [Osteoarthritis due to Pseudallescheria boydii in a patient with acute lymphoblastic lymphoma: report of a case]. Rev Méd Interne 1999; 20: 434–438
   PubMed Web of Science ®Google Scholar
• Ansari RA, Hindson DA, Stevens DL, Kloss JG. Pseudallescheria boydii arthritis and osteomyelitis in a patient with Cushing's disease. South Med J 1987; 80: 90–92
   PubMed Web of Science ®Google Scholar
• Haapasaari J, Essen RV, Kahanpää A, et al. Fungal arthritis simulating juvenile rheumatoid arthritis. Br Med J 1982; 285(6346)923–924
   PubMedGoogle Scholar
• Hung LH, Norwood LA. Osteomyelitis due to Pseudallescheria boydii. South Med J 1993; 86: 231–234
   PubMed Web of Science ®Google Scholar
• Levine NB, Kurokawa R, Fichtenbaum CJ, Howington JA, Kuntz C. An immunocompetent patient with primary Scedosporium apiospermum vertebral osteomyelitis. J Spinal Disord Tech 2002; 15: 425–430
   PubMed Web of Science ®Google Scholar
• Lang AG, Peterson HA. Osteomyelitis following puncture wounds of the foot in children. J Trauma 1976; 16: 993–999
   PubMedGoogle Scholar
• Lonser RR, Brodke DS, Dailey AT. Vertebral osteomyelitis secondary to Pseudallescheria boydii. J Spinal Disord 2001; 14: 361–364
   PubMedGoogle Scholar
• GattoJ, Paterson D, Davis L, Lockwood L, Allworth A. Vertebral osteomyelitis due to Pseudallescheria boydii. Pathology 1997; 29: 238–240
   PubMedGoogle Scholar
• German JW, Kellie SM, Pai MP, Turner PT. Treatment of a chronic Scedosporium vertebral osteomyelitis. Neurosurg Focus 2004; 17: 1–8
   Google Scholar
• Halpern AA, Nagel DA, Schurman DJ. Allescheria boydii osteomyelitis following multiple steroid injections and surgery. Clin Orthop Related Res 1977; 126: 232–234
   Google Scholar
• Sydnor MK, Kaushik S, Knight TE, Bridges CL, McCarty JM. Mycotic osteomyelitis due to Scedosporium apiospermum: MR imaging–pathologic correlation. Skeletal Radiol 2003; 32: 656–660
   PubMed Web of Science ®Google Scholar
• Ernest JT, Rippon JW. Keratitis due to Allescheria boydii (Monosporium apiospermum). Am J Ophthalmol 1966; 62: 1202–1204
   PubMedGoogle Scholar
• Diaz-Valle D, Benitez del Castillo JM, Amor E, et al. Severe keratomycosis secondary to Scedosporium apiospermum. Cornea 2002; 21: 516–518
   PubMed Web of Science ®Google Scholar
• Del Palacio A, Perez–Blazquez E, Cuetara MS, et al. Keratomycosis due to Scedosporium apiospermum. Mycoses 1991; 34: 483–487
   PubMedGoogle Scholar
• Orr PH, Safneck JR, Napier LB. Monosporium apiospermum endophthalmitis in a patient without risk factors for infection. Can J Ophthalmol 1993; 28: 187–190
   PubMedGoogle Scholar
• Ruesch R, Buchi ER, Bischoff P, Schneider P. Pseudallescheria-boydii-Pilzendophthalmitis 6 Jahre nach Trabekulektomie [Endophthalmitis due to Pseudallescheria boydii 6 years after trabeculectomy]. Klin Monatsbl Augenheilkd 1994; 204: 468–469
   PubMedGoogle Scholar
• Chander J, Sharma A. Prevalence of fungal corneal ulcers in northern India. Infection 1994; 22: 207–209
   PubMed Web of Science ®Google Scholar
• McKelvie PA, Wong EY, Chow LP, Hall AJ. Scedosporium endophthalmitis: two fatal disseminated cases of Scedosporium infection presenting with endophthalmitis. Clin Experim Ophthalmol 2001; 29: 330–334
   PubMedGoogle Scholar
• McGuire TW, Bullock JD, Bullock JD, Jr, Elder BL, Funkhouser JW. Fungal endophthalmitis. An experimental study with a review of 17 human ocular cases. Arch Ophthalmol 1991; 109: 1289–1296
   PubMedGoogle Scholar
• D'Hondt K, Parys–van Ginderdeuren R, Foets B. Fungal keratitis caused by Pseudallescheria boydii (Scedosporium apiospermum). Bull Soc Belge Ophthalmol 2000; 277: 53–56
   Google Scholar
• Thomas PA. Current perspectives on ophthalmic mycoses. Clin Microbiol Rev 2003; 16: 730–797
   PubMed Web of Science ®Google Scholar
• Köhler U. Entzündlicher Tränen-Nasenwegsverschluß durch Monosporium apiospermum (Allescheria boydii) [Inflammatory occlusion of the lachrymal duct by Monosporium apiospermum (Allescheria boydii)]. Klin Monatsbl Augenheilkd 1982; 181: 480–482
   PubMedGoogle Scholar
• Garcia-Martos P, Dominguez I, Marin P, et al. Onicomicosis por hongos filamentosos no dermatófitos en Cadiz [Onychomycosis by non-dermatophyte filamentous fungi in Cadiz]. Enferm Infecc Microbiol Clin 2000; 18: 319–324
   PubMedGoogle Scholar
• Summerbell RC. Nondermatophytic molds causing dermatophytosis-like nail and skin infection. Laboratory Handbook of Dermatophytes, J Kane, R Summerbell, L Sigler, S Krajden, G Land. Star Publ, BelmontUSA 1997; 213–259
   Google Scholar
• Uenotsuchi T, Moroi Y, Urabe K, et al. Cutaneous Scedosporium apiospermum infection in an immunocompromised patient and review of the literature. Acta Derm Venereol 2005; 85: 156–159
   PubMed Web of Science ®Google Scholar
• Miele PS, Levy CS, Smith MA, et al. Primary cutaneous fungal infections in solid organ transplantation: a case series. Am J Transpl 2002; 2: 678–683
   PubMed Web of Science ®Google Scholar
• Karaarslan A, Arikan S, Karaarslan F, Cetin ES. Skin infection caused by Scedosporium apiospermum. Mycoses 2003; 46: 524–526
   PubMedGoogle Scholar
• Schaenman JM, DiGiulio DB, Mirels LF, et al. Scedosporium apiospermum soft tissue infection successfully treated with voriconazole: potential pitfalls in the transition from intravenous to oral therapy. J Clin Microbiol 2005; 43: 973–977
   PubMed Web of Science ®Google Scholar
• Cremer G, Bournerias I, Mhalla S, et al. Scédosporiose cutanée non mycétomateuse chez un patient immunodéprimé [Non–mycetoma cutaneous scedosporiosis in an immunocompromised patient]. J Mycol Med 1994; 4: 111–114
   Google Scholar
• Sheftel TG, Mader JT, Cierny G. Pseudoallescheria boydii soft tissue abscess. Clin Orthop 1987; 215: 212–216
   Google Scholar
• Conti-Díaz IA. Micetomas y procesos premicetomatosos en el Uruguay [Mycetoma and pre-mycetomatic infections in Uruguay]. Mycopathologia 1980; 72: 59–64
   PubMedGoogle Scholar
• Kusne S, Ariyanayagam-Baksh S, Strollo DC, Abernethy J. Invasive Scedosporium apiospermum infection in a heart transplant recipient presenting with multiple skin nodules and a pulmonary consolidation. Transpl Infect Dis 2000; 2: 94–196
   Google Scholar
• Torok L, Simon G, Csornai A, Tapai M, Torok I. Scedosporium apiospermum infection imitating lymphocutaneous sporotrichosis in a patient with myeloblastic-monocytic leukaemia. Br J Dermatol 1995; 133: 805–809
   PubMed Web of Science ®Google Scholar
• Kiraz N, Gulbas Z, Akgun Y, Uzun O. Lymphadenitis caused by Scedosporium apiospermum in an immunocompetent patient. Clin Infect Dis 2001; 32: E59–E61
   PubMed Web of Science ®Google Scholar
• Canet JJ, Pagerols X, Sanchez C, Vives P, Garau J. Lymphocutaneous syndrome due to Scedosporium apiospermum. Clin Microbiol Infect 2001; 7: 648–650
   PubMed Web of Science ®Google Scholar
• Gluckman SJ, Ries K, Abrutynm E. Allescheria (Petriellidium) boydii sinusitis in a compromised host. J Clin Microbiol 1977; 5: 481–484
   PubMedGoogle Scholar
• Mader JT, Ream RS, Heath PW. Petriellidium boydii (Allescheria boydii) sphenoidal sinusitis. JAMA 1978; 239: 2368–2369
   PubMedGoogle Scholar
• Morgan MA, Wilson WR, Neel HB, Roberts GD. Fungal sinusitis in healthy and immunocompromised individuals. Am J Clin Pathol 1984; 82: 597–601
   PubMed Web of Science ®Google Scholar
• Erris DJ, Steiniger JR. Scedosporium apiospermum – fungal sinusitis in an immunocompetent patient. Am J Rhinol 1992; 6: 49–53
   Google Scholar
• Kauffman CA. Fungal infections. Infect Med 2003; 20: 424–436
   Google Scholar
• Thiagalingam S, Fernando GT, Tan K, et al. Orbital apex syndrome secondary to Pseudallescheria boydii fungal sinusitis in an immunocompetent patient. Clin Exper Ophthalmol 2004; 32: 45–547
   Google Scholar
• Bryan CS, Disalvo AF, Kaufman L, et al. Petriellidium boydii infection of the sphenoid sinus. Am J Pathol 1980; 74: 846–851
   Google Scholar
• Winn RE, Ramsey PD, McDonald JC, Dunlop KJ. Maxillary sinusitis from Pseudallescheria boydii. Efficacy of surgical therapy. Arch Otolaryngol 1983; 109: 123–125
   PubMedGoogle Scholar
• Salitan ML, Lawson M, Som PM, Bottone EJ, Biller HF. Pseudallescheria sinusitis with intracranial extension in a nonimmunocompromised host. Otolaryngol. Head Neck Surg 1990; 102: 745–750
   Google Scholar
• Shaw CL, McCleave M, Wormald PJ. Unusual presentations of isolated sphenoid fungal sinusitis. J Laryngol Otol 2000; 114: 385–388
   PubMedGoogle Scholar
• Stamm MA, Frable MA. Invasive sinusitis due to Pseudallescheria boydii in an immunocompetent host. South Med J 1992; 85: 439–441
   PubMedGoogle Scholar
• Del Palacio A, Garau M, Tena D, et al. Otitis externa por Scedosporium apiospermum. Revta Iberoam Micol 1999; 16: 161–163
   PubMedGoogle Scholar
• Bhally HS, Shields C, Lin SY, Merz WG. Otitis caused by Scedosporium apiospermum in an immunocompetent child. Int J Pediatr Otorhinolaryngol 2004; 68: 975–978
   PubMedGoogle Scholar
• Gugnani HC, Okafor BC, Njoku-Obi ANU. Etiological agents of otomycosis in Nigeria. Mykosen 1987; 32: 224–229
   Google Scholar
• Rippon JW, Carmichael JW. Petriellidiosis (allescheriosis): four unusual cases and review of the literature. Mycopathologia 1976; 58: 117–124
   PubMedGoogle Scholar
• Slack CL, Watson DW, Abzug MJ, Shaw C, Chan KH. Fungal mastoiditis in immunocompromised children. Arch Otolaryngol Head Neck Surg 1999; 125: 73–75
   PubMedGoogle Scholar
• Yao M, Messner AH. Fungal malignant otitis externa due to Scedosporium apiospermum. Ann Otol Rhinol Laryngol 2001; 110: 377–380
   PubMed Web of Science ®Google Scholar
• Kathuria SK, Rippon J. Non-aspergillus aspergilloma. Am J Clin Pathol 1982; 78: 870–873
   PubMedGoogle Scholar
• Severo LC, Londero AT, Picon PD, Rizzon CF, Tarasconi JC. Petriellidium boydii fungus ball in a patient with active tuberculosis. Mycopathologia 1982; 77: 15–17
   PubMedGoogle Scholar
• Adelson HT, Malcolm JA. Endocavitary treatment of pulmonary mycetomas. Am Rev Resp Dis 1968; 98: 87–92
   PubMedGoogle Scholar
• Kwon-Chung, KJ, Bennett, JE ( eds). Medical Mycology. Lea & Febiger, Philadelphia, 1992.
   Google Scholar
• Rippon JW. Clinical spectrum of petriellidosis: mycetoma to systemic opportunistic. Pan Am Health Org Sci Publ 1980; 396: 276–295
   Google Scholar
• Deloach ED, DiBenedetto RJ, Hitch WS, Russell P. Pulmonary infection with Petriellidium boydii. South Med J 1979; 72: 479–481
   PubMedGoogle Scholar
• Stanley MW, Deike M, Knoedler J, Iber C. Pulmonary mycetomas in immunocompetent patients: diagnosis by fine-needle aspiration. Diagn Cytopathol 1992; 8: 577–579
   PubMedGoogle Scholar
• Zaas D. Cases from the Osler Medical Service at Johns Hopkins University. Scedosporium apiospermum mycetoma of the lung. Am J Med 2002; 113: 760–762
   PubMedGoogle Scholar
• Przyjemski CJ. Organ-specific variation in the morphology of the fungomas (fungus balls) of Pseudallescheria boydii. Arch Pathol Lab Med 1989; 113: 1324
   PubMedGoogle Scholar
• Belitsos NJ, Merz WJ, Bowersox DW, Hutchins GM. Allescheria boydii mycetoma complicating pulmonary sarcoid. Johns Hopkins Med J 1974; 135: 259–267
   PubMedGoogle Scholar
• García J, Perkins A, Garau M, et al. Tratamiento eficaz con voriconazol de un fungoma pulmonar por Pseudallescheria boydii en un paciente con infección por VIH y tuberculosis previa [Efficient treatment by voriconazole of a pulmonary fungoma by Pseudallescheria boydii in a patient with preceding HIV infection and tuberculosis]. Revta Iberoam Micol 2003; 20: 64–67
   PubMedGoogle Scholar
• Reddy PC, Christianson CS, Gorelick DF, Larsh HW. Pulmonary monosporosis: an uncommon pulmonary mycotic infection. Thorax 1969; 24: 722–728
   PubMedGoogle Scholar
• Severo LC, Oliveira FM, Irion K. Respiratory tract intracavitary colonization due to Scedosporium apiospermum; report of four cases. Rev Inst Med Trop Sao Paulo 2004; 46: 43–46
   PubMedGoogle Scholar
• Rosen P, Adelson HT, Burleigh E. Bronchiectasis complicated by the presence of Monosporium apiospermum and Aspergillus fumigatus. Am J Clin Pathol 1969; 52: 182–187
   PubMedGoogle Scholar
• Tong JL, Valentine EH, Durrance JR, Wilson GM, Fischer DA. Pulmonary infection with Allescheria boydii; report of a fatal case. Am Rev Tuberc 1958; 78: 604–609
   PubMedGoogle Scholar
• Travis RE, Ulrich EW, Phillips S. Pulmonary allescheriasis. Ann Intern Med 1961; 4: 141–152
   Google Scholar
• Miller MA, Greenberger PA, Amerian A, et al. Allergic bronchopulmonary mycosis caused by Pseudallescheria boydii. Am Rev Respir Dis 1993; 148: 810–812
   PubMedGoogle Scholar
• Greenberger PA. Allergic bronchopulmonary aspergillosis. J Allergy Clin Immunol 1984; 74: 645–653
   PubMedGoogle Scholar
• Carles P, Recco P, Fournial F, et al. Alleschériose pulmonaire [Pulmonary allescheriosis]. Poumon Coeur 1979; 35: 101–104
   PubMedGoogle Scholar
• Hainer JW, Ostrow JH, Mackenzie DW. Pulmonary monosporosis: report of a case with precipitating antibody. Chest 1974; 66: 601–603
   PubMed Web of Science ®Google Scholar
• Milne LJ, McKerrow WS, Paterson WD, Petrie GR, Postlethwaite R. Pseudallescheriasis in northern Britain. J Med Vet Mycol 1986; 24: 377–382
   PubMedGoogle Scholar
• Beguin H, Nolard N. Mould diversity in homes. Air and surface analysis of 130 dwellings. Aerobiologia 1994; 10: 157–166
   Google Scholar
• Del Palacio A, Garau M, Amor E, et al. Case reports. Transient colonization with Scedosporium prolificans. Report of four cases in Madrid. Mycoses 2001; 44: 321–325
   PubMedGoogle Scholar
• Lake FR, Tribe AE, McAleer R, Froudist J, Thompson PJ. Mixed allergic bronchopulmonary fungal disease due to Pseudallescheria boydii and Aspergillus. Thorax 1990; 45: 489–491
   PubMed Web of Science ®Google Scholar
• Chabasse D, Bouchara JP, Chazalette JP, et al. Mucoviscidose et colonisation fongique à Scedosporium apiospermum [Mucoviscidosis and fungal colonization by Scedosporium apiospermum]. J Mycol Méd 1991; 1: 152–155
   Google Scholar
• Koch C, Hoiby N. Pathogenesis of cystic fibrosis. Lancet 1993; 341: 1065–1069
   PubMed Web of Science ®Google Scholar
• Haase, G, Peltroche-Llacsahuanga, H, Döhmen, H. Identification of fungi recovered from sputum of patients with cystic fibrosis (CF) by sequence analysis of the D1/D2 domain of the nuclear LSU rDNA, Mycoses 2004; 47: 361 ( Abstract).
   Google Scholar
• Tamm M, Malouf M, Glanville A. Pulmonary Scedosporium infection following lung transplantation. Transpl Infect Dis 2001; 3: 189–194
   PubMedGoogle Scholar
• Louria DB, Lieberman PH, Collins HS, Blevins A. Pulmonary mycetoma due to Allescheria boydii. Arch Intern Med 1966; 117: 748–751
   PubMedGoogle Scholar
• Bakerspigel A, Wood T, Burke S. Pulmonary allescheriasis: report of a case from Ontario, Canada. Am J Clin Pathol 1977; 68: 299–303
   PubMedGoogle Scholar
• Horré R, Jovanic B, Marklein G, et al. Fatal pulmonary scedosporiosis. Mycoses 2003; 46: 418–421
   PubMed Web of Science ®Google Scholar
• Tekavec J, Mlinaric-Missoni E, Babic-Vazic V. Pulmonary tuberculosis associated with invasive pseudallescheriasis. Chest 1997; 111: 508–511
   PubMed Web of Science ®Google Scholar
• Seale JP, Hudson JA. Successful medical treatment of pulmonary petriellidiosis. South Med J 1985; 78: 473–476
   PubMedGoogle Scholar
• Bousley PH. Isolation of Allescheria boydii from pleural fluid. J Clin Microbiol 1977; 5: 244
   PubMedGoogle Scholar
• Hung CC, Chang SC, Yang PC, Hsieh WC. Invasive pulmonary pseudallescheriasis with direct invasion of the thoracic spine in an immunocompetent patient. Eur J Clin Microbiol Infect Dis 1994; 13: 749–751
   PubMed Web of Science ®Google Scholar
• Verweij PE, Cox NJ, Meis JF. Oral terbinafine for treatment of pulmonary Pseudallescheria boydii infection refractory to itraconazole therapy. Eur J Clin Microbiol Infect Dis 1997; 16: 26–28
   PubMed Web of Science ®Google Scholar
• Galgiani JN, Stevens DA, Graybill JR, et al. Pseudallescheria boydii infections treated with ketoconazole. Clinical evaluations of seven patients and in vitro susceptibility results. Chest 1984; 86: 219–224
   PubMed Web of Science ®Google Scholar
• Saadah HA, Dixon T. Petriellidium boydii (Allescheria boydii). Necrotizing pneumonia in a normal host. JAMA 1981; 245: 605–606
   PubMedGoogle Scholar
• Yano S, Shishido S, Toritani T, Yoshida K, Nakano H. Intrabronchial pseudallescheriasis in an immunocompetent woman. Clin Infect Dis 1997; 24: 735–736
   PubMedGoogle Scholar
• O'Bryan TA, Browne FA, Schonder JF. Scedosporium apiospermum (Pseudallescheria boydii) endocarditis. J Infect 2002; 44: 189–192
   PubMed Web of Science ®Google Scholar
• Armin AR, Reddy VB, Orfei E. Fungal endocarditis caused by Pseudallescheria (Petriellidium) boydii in an intravenous drug abuser. Tex Heart Inst J 1987; 14: 321–324
   PubMedGoogle Scholar
• Gordon G, Axelrod JL. Case report: prosthetic valve endocarditis caused by Pseudallescheria boydii and Clostridium limosum. Mycopathologia 1985; 89: 129–134
   PubMedGoogle Scholar
• Roberts FJ, Allen P, Maybee TK. Petriellidium boydii (Allescheria boydii) endocarditis associated with porcine valve replacement. Can Med Assoc J 1977; 117: 1250–1252
   PubMedGoogle Scholar
• Welty FK, McLeod GH, Ezratty C, Healy RW, Karchmer AW. Pseudallescheria boydii endocarditis of the pulmonic valve in a liver transplant recipient. Clin Infect Dis 1992; 15: 858–860
   PubMedGoogle Scholar
• Zafiro A. Forma singolare di mycosi cutanea da Monosporium apiospermum a sviluppo clinicamente setticemico. Giorn Med Mil 1938; 86: 636–640
   Google Scholar
• Montejo M, Muniz ML, Zarraga S, et al. Infection due to Scedosporium apiospermum in renal transplant recipients: a report of two cases and literature review of central nervous system and cutaneous infections by Pseudallescheria boydii/Sc. apiospermum. Mycoses 2002; 45: 418–427
   PubMed Web of Science ®Google Scholar
• Bower CP, Oxley JD, Campbell CK, Archer CB. Cutaneous Scedosporium apiospermum infection in an immunocompromised patient. J Clin Pathol 1999; 52: 846–848
   PubMed Web of Science ®Google Scholar
• Bernstein EF, Schuster MG, Stieritz DD, Heuman PC, Uitto J. Disseminated cutaneous Pseudallescheria boydii. Br J Dermatol 1995; 132: 456–460
   PubMed Web of Science ®Google Scholar
• Gompels MM, Bethune CA, Jackson G, Spickett GP. Scedosporium apiospermum in chronic granulomatous disease treated with an HLA matched bone marrow transplant. J Clin Pathol 2002; 55: 784–786
   PubMed Web of Science ®Google Scholar
• Khurshid A, Barnett VT, Sekosan M, Ginzburg AS, Onal E. Disseminated Pseudallescheria boydii infection in a nonimmunocompromised host. Chest 1999; 116: 572–574
   PubMed Web of Science ®Google Scholar
• Nguyen BD. Pseudallescheriasis of the lung and central nervous system: multimodality imaging. Am J Roentgenol 2001; 176: 257–258
   PubMed Web of Science ®Google Scholar
• Riddell J, Chenoweth CE, Kauffman CA. Disseminated Scedosporium apiospermum infection in a previously healthy woman with HELLP syndrome. Mycoses 2004; 47: 442–446
   PubMed Web of Science ®Google Scholar
• Selby R. Pachymeningitis secondary to Allescheria boydii. Case report. J Neurosurg 1972; 36: 225–227
   PubMedGoogle Scholar
• Sanchez-Sousa A, Leon A, Perez DO, et al. Pseudallescheria boydii genitourinary infection during bladder catheterization in a leukaemic patient. J Med Vet Mycol 1992; 30: 79–81
   PubMedGoogle Scholar
• Horré R., Feil E., Stangel A. P., et al. Scedosporiosis of the brain with fatal outcome after traumatization of the foot. Mycoses 2000; 43(Suppl 2)33–36
   PubMedGoogle Scholar
• Campagnaro EL, Woodside KJ, Early MJ, et al. Disseminated Pseudallescheria boydii (Scedosporium apiospermum) infection in a renal transplant patient. Transpl Infect Dis 2002; 4: 207–211
   PubMedGoogle Scholar
• Lopez FA, Crowley RS, Wastila L, Valantine HA, Remington JS. Scedosporium apiospermum (Pseudallescheria boydii) infection in a heart transplant recipient: a case of mistaken identity. J Heart Lung Transpl 1998; 17: 321–324
   PubMed Web of Science ®Google Scholar
• Horré G, de Hoog GS. Primary cerebral infections by melanized fungi: a review. Stud Mycol 1999; 43: 176–194
   Google Scholar
• Scherr GR, Evans SG, Kiyabu MT, Klatt EC. Pseudallescheria boydii infection in the acquired immunodeficiency syndrome. Arch Pathol Lab Med 1992; 116: 535–536
   PubMed Web of Science ®Google Scholar
• Segal BH, Bow EJ, Menichetti F. Fungal infections in nontransplant patients with hematologic malignancies. Infect Dis Clin North Am 2002; 16: 935–964
   PubMed Web of Science ®Google Scholar
• Wilichowski E, Christen HJ, Schiffmann H, Schulz-Schaeffer W, Behrens-Baumann W. Fatal Pseudallescheria boydii panencephalitis in a child after near-drowning. Pediatr Infect Dis J 1996; 15: 365–370
   PubMedGoogle Scholar
• Dworzack DL, Clark RB, Borkowski WJ, Jr, et al. Pseudallescheria boydii brain abscess: association with near-drowning and efficacy of high-dose, prolonged miconazole therapy in patients with multiple abscesses. Medicine (Baltimore) 1989; 68: 218–224
   PubMed Web of Science ®Google Scholar
• Farina C, Arosio M, Marchesi G, Amer M. Scedosporium apiospermum post–traumatic cranial infection. Brain Inj 2002; 16: 627–631
   PubMed Web of Science ®Google Scholar
• Tan TY, Liou CW, Kung LC. Meningitis caused by Pseudallescheria boydii. Chang Gung Med J 2004; 27: 228–232
   PubMedGoogle Scholar
• Tadros TS, Workowski KA, Siegel RJ, Hunter S, Schwartz DA. Pathology of hyalohyphomycosis caused by Scedosporium apiospermum (Pseudallescheria boydii): an emerging mycosis. Hum Pathol 1998; 29: 1266–1272
   PubMed Web of Science ®Google Scholar
• Luu KK, Scott IU, Miller D, Davis JL. Endogenous Pseudallescheria boydii endophthalmitis in a patient with ring-enhancing brain lesions. Ophthalmic Surg Lasers 2001; 32: 325–329
   PubMedGoogle Scholar
• Messori A, Lanza C, De Nicola M, et al. Mycotic aneurysms as lethal complication of brain pseudallescheriasis in a near-drowned child: a CT demonstration. Am J Neuroradiol 2002; 23: 1697–1699
   PubMed Web of Science ®Google Scholar
• Watson JC, Myseros JS, Bullock MR. True fungal mycotic aneurysm of the basilar artery: a clinical and surgical dilemma. Cerebrovasc Dis 1999; 9: 50–53
   PubMedGoogle Scholar
• Aronson SM, Benham R, Wolf A. Maduromycosis of the central nervous system. J Neuropathol Exp Neurol 1953; 12: 158–168
   PubMedGoogle Scholar
• Schwartz DA, Amenta PS, Finkelstein SD. Cerebral Pseudallescheria boydii infection: unique occurrence of fungus ball formation in the brain. Clin Neurol Neurosurg 1989; 91: 79–84
   PubMedGoogle Scholar
• Enggano IL, Hughes WT, Kalwinsky DK, et al. Pseudallescheria boydii in a patient with acute lymphoblastic leukemia. Arch Pathol Lab Med 1984; 108: 619–622
   PubMedGoogle Scholar
• Hofman P, Saint-Paul MC, Gari-Toussaint M, et al. Infection disséminée à Scedosporium apiospermum chez un transplanté hépatique. Un diagnostic différentiel de l'aspergillose invasive [Disseminated infection due to Scedosporium apiospermum in a liver transplant recipient. Differential diagnostics with invasive aspergillosis]. Ann Pathol 1993; 13: 332–335
   PubMedGoogle Scholar
• Rosen F, Deck JH, Rewcastle NB. Allescheria boydii – unique systemic dissemination to thyroid and brain. Can Med Assoc J 1965; 93: 1125–1127
   PubMedGoogle Scholar
• Walker DH, Adamec T, Krigman M. Disseminated petriellidosis (allescheriosis). Arch Pathol Lab Med 1978; 102: 158–160
   PubMed Web of Science ®Google Scholar
• Chaney S, Gopalan R, Berggren RE. Pulmonary Pseudallescheria boydii infection with cutaneous zygomycosis after near drowning. South Med J 2004; 97: 683–687
   PubMed Web of Science ®Google Scholar
• Meadow WL, Tipple MA, Rippon JW. Endophthalmitis caused by Petriellidium boydii. Am J Dis Child 1981; 135: 378–380
   PubMedGoogle Scholar
• Kowacs PA, Soares Silvado CE, Monteiro DA, et al. Infection of the CNS by Scedosporium apiospermum after near drowning. Report of a fatal case and analysis of its confounding factors. J Clin Pathol 2004; 57: 205–207
   PubMed Web of Science ®Google Scholar
• Garzoni C, Emonet S, Legout L., et al. Atypical infections in tsunami survivors. Emerg Infect Dis 2005; 11: 1591–1593
   PubMed Web of Science ®Google Scholar
• Ender PT, Dolan MJ. Pneumonia associated with near-drowning. Clin Infect Dis 1997; 25: 896–907
   PubMed Web of Science ®Google Scholar
• Gugnani HC. Fungi isolated from lungs of small wild animals in India. Mykosen 1972; 15: 479–482
   PubMedGoogle Scholar
• Ramirez R, Robertstad GW, Hutchinson LR, Chavez J. Mycotic flora in the lower digestive tract of feral pigeons (Columba livia) in the El Paso, Texas area. J Wildl Dis 1976; 12: 83–85
   PubMedGoogle Scholar
• Gugnani HC, Okafor JI. Mycotic flora of the intestine and other internal organs of certain reptiles and amphibians with special reference to characterization of Basidiobolus isolate. Mykosen 1979; 23: 260–268
   Google Scholar
• Friedman DS, Schoster JV, Pickett JP, et al. Pseudallescheria boydii keratomycosis in a horse. J Am Vet Med Assoc 1989; 195: 616–618
   PubMedGoogle Scholar
• Smedes SL, Miller PE, Dubielzig RR. Pseudallescheria boydii keratomycosis in a dog. J Am Vet Med Assoc 1992; 200: 199–202
   PubMedGoogle Scholar
• Allison N, McDonald RK, Guist SR, Bentinck-Smith J. Eumycotic mycetoma caused by Pseudallescheria boydii in a dog. J Am Vet Med Assoc 1989; 194: 797–799
   PubMed Web of Science ®Google Scholar
• Kurtz HJ, Finco DR, Perman V. Maduromycosis (Allescheria boydii) in a dog. J Am Vet Med Assoc 1970; 157: 917–921
   PubMedGoogle Scholar
• Johnson GR, Schiefer B, Pantekoek JF. Maduromycosis in a horse in western Canada. Can Vet J 1975; 16: 341–344
   PubMedGoogle Scholar
• McEntee M. Eumycotic mycetoma: review and report of a cutaneous lesion caused by Pseudallescheria boydii in a horse. J Am Vet Med Assoc 1987; 191: 1459–1461
   PubMedGoogle Scholar
• Walker RL, Monticello TM, Ford RB, English RV. Eumycotic mycetoma caused by Pseudallescheria boydii in the abdominal cavity of a dog. J Am Vet Med Assoc 1988; 192: 67–70
   PubMedGoogle Scholar
• Cabañes FJ, Roura X, Garcia F, et al. Nasal granuloma caused by Scedosporium apiospermum in a dog. J Clin Microbiol 1998; 36: 2755–2758
   PubMed Web of Science ®Google Scholar
• Coleman MG, Robson MC. Nasal infection with Scedosporium apiospermum in a dog. N Z Vet J 2004; 53: 81–83
   Google Scholar
• Davis PR, Meyer GA, Hanson RR, Stringfellow JS. Pseudallescheria boydii infection of the nasal cavity of a horse. J Am Vet Med Assoc 2000; 217: 707–709
   PubMed Web of Science ®Google Scholar
• Pawaiya RV, Charan K, Sikdar A, Parihar NS. Invasive pulmonary pseudallescheriosis in a cross–breed calf. Mycopathologia 1994; 128: 9–11
   PubMedGoogle Scholar
• Carter ME, di Menna ME. Letter: Petriellidium boydii from the reproductive tracts of mares. N Z Vet J 1975; 23: 13
   PubMedGoogle Scholar
• Mahaffey LW, Rossdale PD. An abortion due to Allescheria boydii and general observations concerning mycotic abortions of mares. Vet Rec 1965; 77: 541–545
   PubMed Web of Science ®Google Scholar
• Eustis SL, Kirkbride CA, Gates C, Haley LD. Porcine abortions associated with fungi, actinomycetes, and Rhodococcus sp. Vet Pathol 1981; 18: 608–613
   PubMedGoogle Scholar
• Knudtson WU, Kirkbride CA. Fungi associated with bovine abortion in the northern plains states (USA). J Vet Diagn Invest 1992; 4: 181–185
   PubMedGoogle Scholar
• Baszler T, Chandler FW, Bertoy RW, Smith CW, Whiteley HE. Disseminated pseudallescheriasis in a dog. Vet Pathol 1988; 25: 95–97
   PubMedGoogle Scholar
• Käufer I, Weber A. Graphium fructicola als Ursache einer Systemmykose beim Hund [Graphium fructicola as a cause of a systemic mycosis in the dog]. Mykosen 1977; 20: 39–46
   PubMedGoogle Scholar
• Watt PR, Robins GM, Galloway AM, O'Boyle DA. Disseminated opportunistic fungal disease in dogs: 10 cases. J Am Vet Med Assoc ; 207 1982; 1995: 67–70
   Google Scholar
• Haulena M, Buckles E, Gulland FM, et al. Systemic mycosis caused by Scedosporium apiospermum in a stranded northern elephant seal (Mirounga angustirostris) undergoing rehabilitation. J ZooWildl Med 2002; 33: 166–171
   PubMed Web of Science ®Google Scholar
• Kuwano A, Yoshihara T, Takatori K, Kosuge J. Onychomycosis in white line disease in horses: pathology, mycology and clinical features. Equine Vet J 1998; 26: 27–35
   Google Scholar
• Travis LB, Roberts GD, Wilson WR. Clinical significance of Pseudallescheria boydii: a revision of 10 years’ experience. Mayo Clin Proc 1985; 60: 531–537
   PubMed Web of Science ®Google Scholar
• Kanafani ZA, Comair Y, Kanj SS. Pseudallescheria boydii cranial osteomielitis and subdural empyema successfully treated with voriconazole: a case report and literature review. Eur J Clin Microbiol Infect Dis 2004; 23: 836–840
   PubMed Web of Science ®Google Scholar
• Willemsem R, Schots S, Shahabpour M, Pierard D. Pseudallescheria boydii tendosynovitis. J Mycol Med 1997; 7: 100–105
   Google Scholar
• Bloom SM, Warner RRP, Weitzman I. Maxillary sinusitis: isolation of Scedosporium (Monosporium) apiospermum, anamorph of Petriellidium (Allescheria) boydii. The Mount Sinai J Med 1982; 49: 492–494
   PubMedGoogle Scholar
• Washburn RG, Kennedy DW, Begley MG, Henderson DK, Bennett JE. Chronic fungal sinusitis in apparently normal hosts. Medicine 1988; 67: 231–247
   PubMed Web of Science ®Google Scholar
• Terris DJ, Steiniger JR. Scedosporium apiospermum – fungal sinusitis in an immunocompetent patient. Am J Rhinol 1992; 6: 49–53
   Google Scholar
• Kusuhara M, Hachisuka H. Lymphocutaneous infection due to Scedosporium apiospermum. Int J Dermatol 1997; 36: 684–688
   PubMed Web of Science ®Google Scholar
• Horré R, Schumacher G, Marklein G, et al. Mycetoma due to Pseudallescheria boydii and co-isolation of Nocardia abscessus in a patient injured in road accident. Med Mycol 2002; 40: 525–527
   PubMed Web of Science ®Google Scholar
• Liu YF, Zhao XD, Ma CL, et al. Cutaneous infection by Scedosporium apiospermum and its successful treatment with itraconazole. Clin Exp Dermatol 1997; 22: 192–200
   PubMedGoogle Scholar
• Lemerle E, Bastien M, Demolliens-Dreux G, et al. Scédosporiose cutanée révélée par un purpura bullo-nécrotique [Cutaneous scedospopriosis revealed by a bullous purpura]. Ann Dermatol Venereol 1998; 125: 711–714
   PubMedGoogle Scholar
• Bosma F, Voss A, van Hamersvelt HW, et al. Two cases of subcutaneous Scedosporium apiospermum infection treated with voriconazole. Clin Microbiol Infect 2003; 9: 750–753
   PubMed Web of Science ®Google Scholar
• Lai TF, Malhotra R, Esmail–Zaden R, et al. Use of voriconazole in Scedosporium apiospermum keratitis. Cornea 2003; 22: 391–392
   PubMedGoogle Scholar
• Wu Z, Ying H, Yiu S, Irvine J, Smith R. Fungal keratitis caused by Scedosporium apiospermum: report of two cases and review of treatment. Cornea 2002; 21: 519–523
   PubMed Web of Science ®Google Scholar
• Saracli MA, Erdem U, Gonlum A, Yildiran ST. Scedosporium apiospermum keratitis treated with itraconazole. Med Mycol 2003; 41: 111–114
   PubMed Web of Science ®Google Scholar
• Hernandez PC, Llinares TF, Burgos SJ, et al. Voriconazole in fungal keratitis caused by Scedosporium apiospermum. Ann Pharmacother 2004; 38: 414–417
   PubMedGoogle Scholar
• Nulens E, Eggink C, Rijs AJ, Wesseling P, Verweij PE. Keratitis caused by Scedosporium apiospermum successfully treated with a cornea transplant and voriconazole. J Clin Microbiol 2003; 41: 2261–2264
   PubMed Web of Science ®Google Scholar
• Verghese S, Padmaja P, Chellamma MT, Leelavathy S, Nayar P. Prosthetic valve endocarditis caused by Scedosporium apiospermum. Indian J Med Microbiol 2005; 23: 264–266
   PubMedGoogle Scholar
• Sobottka I, Deneke J, Pothmann W, Heinemann A, Mack D. Fatal native valve endocarditis due to Scedosporium apiospermum (Pseudallescheria boydii) following trauma. Eur J Clin Microbiol Infect Dis 1999; 18: 387–389
   PubMed Web of Science ®Google Scholar
• Stolk-Engelaar MV, Cox NJ. Successful treatment of pulmonary pseudallescheriasis with itraconazole. Eur J Clin Microbiol Infect Dis 1993; 12: 142
   PubMedGoogle Scholar
• Chakraborty A, Workman MR, Bullock PR. Scedosporium apiospermum brain abscess treated with surgery and voriconazole. Case report. J Neurosurg 2005; 103: 83–87
   PubMedGoogle Scholar
• Huang HJ, Zhu JY, Zhang YH. The first case of Pseudallescheria boydii meningitis in China – electron microscopic study and antigenicity analysis of the agent. J Tongji Med Univ 1990; 10: 218–221
   PubMedGoogle Scholar
• Danaher PJ, Walter EA. Successful treatment of chronic meningitis caused by Scedosporium apiospermum with oral voriconazole. Mayo Clin Proc 2004; 79: 707–708
   PubMed Web of Science ®Google Scholar
• Hachem R, Graybill JR, Negroni R, et al. Posaconazole as salvage therapy for Pseudallescheria infections: a case series. Clin Microbiol Infect 2004; 10(Suppl. 3)510
   Google Scholar
• Mellinghoff IK, Winston, Mukwaya G, Schiller GJ. Treatment of Scedosporium apiospermum brain abscesses with posaconazole. Clin Infect Dis 2002; 34: 1648–1650
   PubMed Web of Science ®Google Scholar
• Fietz T, Knauf W, Schwartz S, Thiel E. Intramedullary abscess in a patient with disseminated Scedosporium apiospermum infection. Br J Haematol 2003; 120: 724
   PubMedGoogle Scholar
• Mursch K, Trnovec S, Ratz H, et al. Successful treatment of multiple Pseudallescheria boydii brain abscesses and ventriculitis/ependymitis in a 2-year-old child after a near-drowning episode. Childs Nerv Syst 2006; 22: 189–192
   PubMedGoogle Scholar
• Jung JY, Salas R, Almond CH, Saab S, Reyna R. The role of surgery in the management of pulmonary monosporosis. A collective review. J Thorac Cardiovasc Surg 1977; 73: 139–144
   PubMedGoogle Scholar
• Muñoz P, Marin M, Tornero P, et al. Successful outcome of Scedosporium apiospermum disseminated infection treated with voriconazole in a patient receiving corticosteroid therapy. Clin Infect Dis 2000; 31: 1499–1501
   PubMed Web of Science ®Google Scholar
• Girmenia C, Luzi G, Monaco M, Martino P. Use of voriconazole in treatment of Scedosporium apiospermum infection: case report. J Clin Microbiol 1998; 36: 1436–1438
   PubMed Web of Science ®Google Scholar
• Ochiai N, Shimazaki C, Uchida R, et al. Disseminated infection due to Scedosporium apiospermum in a patient with acute myelogenous leukemia. Leuk Lymphoma 2003; 44: 369–372
   PubMed Web of Science ®Google Scholar
• Phillips P, Forbes JC, Speert DP. Disseminated infection with Pseudallescheria boydii in a patient with chronic granulomatous disease: response to gamma-interferon plus antifungal chemotherapy. Pediatr Infect Dis J 1991; 10: 536–539
   PubMed Web of Science ®Google Scholar
• Walsh TJ, Lutsar I, Driscoll T, et al. Voriconazole in the treatment of aspergillosis, scedosporiosis and other invasive fungal infections in children. Pediatr Infect Dis J 2002; 21: 240–248
   PubMed Web of Science ®Google Scholar
• Perfect JR, Marr KA, Walsh TJ, et al. Voriconazole treatment for less-common, emerging, or refractory fungal infections. Clin Infect Dis 2003; 36: 1122–1131
   PubMed Web of Science ®Google Scholar
• Warris A, Gaustad P, Meis JF, et al. Recovery of filamentous fungi from water in a paediatric bone marrow transplantation unit. J Hosp Infect 2001; 47: 143–148
   PubMed Web of Science ®Google Scholar
• Fahal AH. Mycetoma: a thorn in the flesh. Trans R Soc Trop Med Hyg 2004; 98: 3–11
   PubMed Web of Science ®Google Scholar