Dermatological disease in Latinos in the USA

References

• Aguirre-Molina M, Molina C. Latino populations: who are they? In: Latino Health in the US: A Growing Challenge. Molina C, Aguirre-Molina M (Eds). American Public Health Association, DC, USA 3–22 (1994).
   Google Scholar
• Taylor SC. Skin of color: biology, structure, function, and implications for dermatologic disease. J. Am. Acad. Dermatol.46, S41–S62 (2002).
   PubMed Web of Science ®Google Scholar
• CDC. Access to Health-Care and Preventive Services Among Latinos and Non-Latinos – United States, 2001–2002. MMWR53, 937–941 (2004)
   PubMedGoogle Scholar
• McLaurin JA. Health care for children of migrant farmworkers. In: Ambulatory Pediatrics (5th Edition). Green M, Haggerty R, Weitzman M (Eds). WB Saunders, PA, USA 524–529 (1999).
   Google Scholar
• Eisenman DP, Gelberg L, Liu H et al. Mental health and health-related quality of life among adult Latino primary care patients living in the United States with previous exposure to political violence. JAMA290, 627–634 (2003).
   PubMed Web of Science ®Google Scholar
• Sanchez MR. Cutaneous diseases in Latinos. Dermatol. Clin.21(4), 689–697 (2003).
   Google Scholar
• Pandya AG, Guevara IL. Disorders of hyperpigmentation. Dermatol. Clin.18(1), 91–98 (2000).
   PubMed Web of Science ®Google Scholar
• Mandry Pagan R, Sanchez JL. Mandibular melasma. Puerto Rico Health Sci. J.19, 231 (2000).
   Google Scholar
• Sialy R, Hassan I, Kaur I et al. Melasma in men: a hormonal profile. J. Am. Acad. Dermatol.27, 64 (2000).
   Google Scholar
• Halder RM, Nootheti PK. Ethnic skin disorders overview. J. Am. Acad. Dermatol.48(6S), 143–148 (2003).
   PubMed Web of Science ®Google Scholar
• Guevara IL, Pandya AG. Melasma treated with hydroquinone, tretinoin, and a fluorinated steroid. Int. J. Dermatol.40(3), 212–215 (2001).
   Google Scholar
• Hardwick N, Van Gelder LW, Van der Merwe CA et al. Exogenous ochronosis: an epidemiological study. Br. J. Dermatol.120(2), 229–238 (1989).
   PubMed Web of Science ®Google Scholar
• Kramer K, Lopez A, Stefanato CM et al. Exogenous ochronosis. J. Am. Acad. Dermatol.42, 869–871 (2000).
   PubMed Web of Science ®Google Scholar
• Mahe A, Ly F, Aymard G et al. Skin diseases associated with the cosmetic use of bleaching products in women from Dakar, Senegal. Br. J. Dermatol.148(3), 493–500 (2003).
   PubMed Web of Science ®Google Scholar
• Sarkar R, Bhalla M, Kanwar AJ. A comparative study of 20 percent azelaic acid cream monotherapy versus a sequential therapy in the treatment of melasma in dark-skinned patients. Dermatology205, 249 (2002).
   PubMed Web of Science ®Google Scholar
• Taylor SC, Torok H, Jones T et al. Efficacy and safety of a new triple-combination agent for the treatment of facial melasma. Cutis72, 67 (2003).
   PubMed Web of Science ®Google Scholar
• Lim JT. Treatment of melasma using kojic acid in a gel containing hydroquinone and glycolic acid. Dermatol. Surg.25(4), 282–284 (1999).
   PubMed Web of Science ®Google Scholar
• Serra-Baldrich E, Tribo MJ, Camarasa JG. Allergic contact dermatitis from kojic acid. Contact Dermatitis39(2), 86–87 (1998).
   PubMed Web of Science ®Google Scholar
• Pinnell SR. Cutaneous photodamage, oxidative stress, and topical antioxidant protection. J. Am. Acad. Dermatol.48(1), 1–19 (2003).
   PubMed Web of Science ®Google Scholar
• Hurley ME, Guevera IL, Gonzales RM et al. Efficacy of glycolic acid peels in the treatment of melasma. Arch. Dermatol.138, 1578–1582 (2002).
   PubMedGoogle Scholar
• Nouri K, Bowes L, Charier T et al. Combination treatment of melasma with pulsed CO2 laser followed by Q-switched alexandrite laser: a pilot study. Dermatol. Surg.25, 494 (1999).
   PubMed Web of Science ®Google Scholar
• Battle EF, Hobbs LM. Laser therapy on darker ethnic skin. Dermatol. Clin.21, 713–723 (2003).
   PubMed Web of Science ®Google Scholar
• Jackson BA. Lasers in ethnic skin: A review. J. Am. Acad. Dermatol.48, S134–S138 (2003).
   Google Scholar
• Victor FC, Gelber J, Rao B. Melasma: a review. J. Cutan. Med. Surg.8(2), 97–102 (2004).
   PubMed Web of Science ®Google Scholar
• Rokhsar CK, Fitzpatrick RE. The treatment of melasma with fractional photothermolysis: a pilot study. Dermatol. Surg.31(12), 1645–1650 (2005).
   PubMed Web of Science ®Google Scholar
• Perez-Bernal A, Munoz-Perez MA, Camacho R. Management of facial hyperpigmentation. Am. J. Clin. Dermatol.1, 261 (2000).
   PubMedGoogle Scholar
• Serrano G, Pujol C, Cuadra J. Riehl’s melanosis: pigmented contact dermatitis caused by fragrances. J. Am. Acad. Dermatol.21, 1057 (1989).
   PubMed Web of Science ®Google Scholar
• Magana-Garcia M, Carrasco E, Herrera-Goepfert R et al. Hyperpigmentation of the clavicular zone: a variant of friction melanosis. Int. J. Dermatol.28(2), 119 (1989).
   Google Scholar
• Osswald SS, Proffer LH, Sartori CR. Erythema dyschromicum perstans: a case report and review. Cutis.68, 25 (2001).
   Google Scholar
• Penagos H, Jimenez V, Fallas V et al. Chlorothalonil, a possible cause of erythema dyschromicum perstans (ashy dermatitis). Contact Dermatitis35, 214 (1996).
   PubMed Web of Science ®Google Scholar
• Baranda L, Torres-Alvarez B, Cortes-Franco R et al. Involvement of cell adhesion and activation molecules in the pathogenesis of erythema dyschromicum perstans (ashy dermatitis). The effect of clofazimine therapy. Arch. Dermatol.133, 325 (1997).
   PubMedGoogle Scholar
• Piquero-Martin J, Perez-Alfonzo R, Abrusci V et al. Clinical trial with clofazimine for treating erythema dyschromicum perstans. Evaluation of cell-mediated immunity. Int. J. Dermatol.28, 198 (1989).
   PubMed Web of Science ®Google Scholar
• Bahadir S, Cobanoglu U, Cimsit G et al. Erythema dyschromicum perstans: response to dapsone therapy. Int. J. Dermatol.43(3), 220–222 (2004).
   PubMedGoogle Scholar
• Jansen T, Gambichler T, von Kobyletzki L et al. Lichen planus actinicus treated with acitretin and topical corticosteroids. Eur. Acad. Dermatol. Venereol.16, 174 (2002).
   Google Scholar
• Albers SE, Glass LF, Fenske NA. Lichen planus subtropicus: direct immunoflourescence findings and therapeutic response to hydroxychloroquine. Int. J. Dermatol.33, 645 (1994).
   PubMed Web of Science ®Google Scholar
• Jang KA, Choi JH, Sung KS et al. Idiopathic eruptive macular pigmentation: report of 10 cases. J. Am. Acad. Dermatol.44, 351 (2001).
   Google Scholar
• Boer A, Misago N, Wolter M et al. Prurigo pigmentosa: a distinctive inflammatory disease of the skin. Am. J. Dermatopathol.25, 117 (2003).
   Google Scholar
• Dereure O. Drug-induced skin pigmentation. Epidemiology, diagnosis and treatment. Am. J. Clin. Dermatol.2(4), 253–262 (2001).
   PubMedGoogle Scholar
• Passeron T, Ostovari N, Zakaria W et al. Topical tacrolimus and the 308-nm excimer laser: a synergistic combination for the treatment of vitiligo. Arch. Dermatol.140(9), 1065–1069 (2004).
   PubMed Web of Science ®Google Scholar
• Hay RJ, Estrada Castanon R, Alarcon Hernandez H et al. Wastage of family income on skin disease in Mexico. Br. Med. J.309, 848 (1994).
   Google Scholar
• Kaya TI, Yazici AC, Tursen U et al. Idiopathic guttate hypomelanosis: idiopathic or ultraviolet induced? Photodermatol. Photoimmunol. Photomed.21(5), 270–271 (2005).
   PubMed Web of Science ®Google Scholar
• Pagnoni A, Kligman AM, Sadiq I et al. Hypopigmented macules of photodamaged skin and their treatment with topical tretinoin. Acta Derm. Venereol.79(4), 305–310 (1999).
   PubMed Web of Science ®Google Scholar
• Hexsel DM. Treatment of idiopathic guttate hypomelanosis by localized superficial dermabrasion. Dermatol. Surg.25(11), 917–918 (1999).
   PubMed Web of Science ®Google Scholar
• Kumarasinghe SP. 3–5 second cryotherapy is effective in idiopathic guttate hypomelanosis. J. Dermatol.31(5), 437–439 (2004).
   PubMed Web of Science ®Google Scholar
• Taylor SC, Cook-Bolden F, Rahman Z et al. Acne vulgaris in skin of color. J. Am. Acad. Dermatol.46, S98–S106 (2002).
   Google Scholar
• Murad H, Shamban AT, Moy LS. Polka-dot syndrome: a more descriptive name for a common problem. Cosmetic Dermatol.2, 57 (1993).
   Google Scholar
• Fitzpatrick SB, Fujii C, Shragg GP et al. Do health care needs of indigent Mexican–American, black, and white adolescents differ? J. Adol. Health Care11, 128 (1990).
   PubMedGoogle Scholar
• Halder RM. The role of retinoids in the management of cutaneous conditions in blacks. J. Am. Acad. Dermatol.39, S98–S103 (1998).
   Google Scholar
• Freyre EA, Rebaza RM, Sami DA et al. The prevalence of facial acne in Peruvian adolescents and its relation to their ethnicity. J. Adol. Health Care22, 480 (1998).
   Google Scholar
• Thiboutot DM, Strauss JS. Diet and acne revisited. Arch. Dermatol.138, 1591 (2002).
   Google Scholar
• Cordain L, Lindeberg S, Hurtado M et al. Acne vulgaris: a disease of Western civilization. Arch. Dermatol.138, 1584 (2002).
   PubMed Web of Science ®Google Scholar
• Jackson BA. Cosmetic considerations and nonlaser cosmetic procedures in ethnic skin. Dermatol. Clin.21, 703–712 (2003).
   Google Scholar
• Cornelison RL. Cutaneous diseases in Native Americans. Dermatol. Clin.21, 699–702 (2003).
   Google Scholar
• Lopez-Gonzalez G. Prurigo solar. Arch. Argent. Dermatol.11, 301–318 (1961).
   Google Scholar
• Magana M, Mendez Y, Rodriguez A et al. The conjunctivitis of solar (actinic) prurigo. Pediatr. Dermatol.17, 432 (2000).
   Google Scholar
• Hojyo-Tomoka T, Granados J, Varga-Alarcon G et al. Further evidence of the role of HLA-DR4 in the genetic susceptibility to actinic prurigo. J. Am. Acad. Dermatol.36, 935 (1997).
   Google Scholar
• Lane PR, Murphy F, Hogan DJ et al. Histopathology of actinic prurigo. Am. J. Dermatopathol.15, 326 (1993).
   Google Scholar
• Herrera-Geopfert R, Magana M. Follicular cheilitis: a distinctive histopathologic finding in actinic prurigo. Am. J. Dermatopathol.17, 357–361 (1995).
   Google Scholar
• Perrett CM, Harwood CA, Khorshid M et al. Primary cutaneous B-cell lymphoma associated with actinic prurigo. Br. J. Dermatol.153, 186–189 (2005).
   Google Scholar
• Lovell CR, Hawk JL, Calnan CD et al. Thalidomide in actinic prurigo. Br. J. Dermatol.108, 467 (1983).
   Google Scholar
• Duran MM, Ordonez CP, Prieto JC et al. Treatment of actinic prurigo in Chimila Indians. Int. J. Dermatol.35, 413 (1996).
   Google Scholar
• Lane PR, Moreland AA, Hogan DJ. Treatment of actinic prurigo with intermittent short-course topical 0.05 percent clobetasol 17-propionate. A preliminary report. Arch Dermatol.126, 1211 (1990).
   Google Scholar
• Las DY, Youn JI, Park MH et al. Actinic prurigo: limited effect of PUVA. Br. J. Dermatol.136, 972 (1997).
   Google Scholar
• Collins P, Ferguson J. Narrow-band UVB (TL-01) phototherapy: an effective preventative treatment for the photodermatoses. Br. J. Dermatol.132, 956 (1995).
   PubMed Web of Science ®Google Scholar
• McCoombes JA, Hirst LW, Green WR. Use of topical cyclosporin for conjunctival manifestations of actinic prurigo. Am. J. Ophthalm.130, 830 (2000).
   Google Scholar
• Torres-Alvarez B, Castanedo-Cazares JP, Moncada B. Pentoxifylline in the treatment of actinic prurigo. Dermatology208, 198–201 (2004).
   Google Scholar
• Wei ML. Hermansky-Pudlak syndrome: a disease of protein trafficking and organelle function. Pigment. Cell Res.19, 19–42 (2006).
   PubMedGoogle Scholar
• Santiago Borrero PJ, Rodriguez-Perez Y, Renta JY et al. Genetic testing for oculocutaneous albinism type 1 and 2 and Hermansky-Pudlak syndrome type 1 and 3 mutations in Puerto Rico. J. Invest. Dermatol.125, 85–90 (2006).
   Google Scholar
• Toro J, Turner M, Gahl WA. Dermatologic manifestations of Hermansky-Pudlak syndrome in patients with and without a 16-base pair duplication in the HPS1 gene. Arch. Dermatol.135, 774 (1999).
   PubMedGoogle Scholar
• Fett DD. Botanical briefs: capsicum peppers. Cuti.72(1), 21–23 (2003).
   Google Scholar
• Lee MR, Shumack S. Prurigo nodularis: a review. Australas. J. Dermatol.46, 211 (2005).
   PubMed Web of Science ®Google Scholar
• Burnett JW. Capsicum pepper dermatitits. Cutis534 (1989).
   Google Scholar
• Jones LA, Tandberg D, Troutman WG. Household treatment for “chile burns” of the hands. Clin. Toxicol.25, 483 (1987).
   Google Scholar
• Stoner JG. Miscellaneous dermatitis-inducing plants. Clin. Dermatol.4, 86–94 (1986).
   Google Scholar
• Kizer WS, Prarie T, Morey AF. Balanitis xerotica obliterans: epidemiologic distribution in an equal access healthcare system. South Med. J.96, 9 (2003).
   PubMed Web of Science ®Google Scholar
• Kiss A, Kiraly L, Kutasy B et al. High incidence of balanitis xerotica obliterans in boys with phimosis: prospective 10-year study. Pediatr. Dermatol.22(4), 305–308 (2005).
   PubMed Web of Science ®Google Scholar
• Drut RM, Gomez MA, Drut R. Human papillomavirus is present in some cases of childhood penile lichen sclerosus: an in situ hybridization and SP-PCR study. Pediatr. Dermatol.15, 85 (1998).
   PubMed Web of Science ®Google Scholar
• Kumaran MS, Kanwar AJ. Squamous cell carcinoma in untreated lichen sclerosus of the penis: a rare complication. J. Dermatol.31(3), 239–241 (2004).
   Google Scholar
• Nasca MR, Innocenzi D, Micali G. Penile cancer among patients with genital lichen sclerosus. J. Am. Acad. Dermatol.41, 911 (1999).
   PubMed Web of Science ®Google Scholar
• Mallon E, Hawkins D, Dinneen M. Circumcision and genital dermatoses. Arch. Dermatol.136, 350 (2000).
   PubMed Web of Science ®Google Scholar
• Vincent MV, Mackinnon E. The response of clinical balanitis xerotica obliterans to the application of topical steroid-based creams. J. Pediatr. Surg.40(4), 709–712 (2005).
   Google Scholar
• Das S, Tunuguntla HS. Balanitis xerotica obliterans – a review. World J. Urol.18(6), 382–387 (2000).
   PubMed Web of Science ®Google Scholar
• Burke JP, Duggirala R, Hale DE et al. Genetic basis of acanthosis nigricans in Mexican Americans and its association with phenotypes related to Type 2 diabetes. Hum. Genet.106, 467 (2000).
   Google Scholar
• Litonjua P, Pinero-Pilona A, Aviles-Santa L et al. Prevalence of acanthosis nigricans in newly-diagnosed Type 2 diabetes. Endocr. Pract.10(2), 101–106 (2004).
   Google Scholar
• Caballero AE. Diabetes in the Latino or Latino population: genes, environment, culture, and more. Curr. Diab. Rep.5(3), 217–225 (2005).
   Google Scholar
• Mukhtar Q, Cleverley G, Voorhees RE et al. Prevalence of acanthosis nigricans and its association with hyperinsulinemia in New Mexico adolescents. J. Adolesc. Health28, 372–376 (2001).
   PubMedGoogle Scholar
• Barbieri RL. Induction of ovulation in infertile women with hyperandrogenism and insulin resistance. Am. J. Obstet. Gynecol.183(6), 1412–1418 (2000).
   Google Scholar
• Hermanns-Le T, Scheen A, Pierard GE. Acanthosis nigricans associated with insulin resistance: pathophysiology and management. Am. J. Clin. Dermatol.5(3), 199–203 (2004).
   PubMed Web of Science ®Google Scholar
• Blobstein SH. Topical therapy with tretinoin and ammonium lactate for acanthosis nigricans associated with obesity. Cutis71(1), 33–34 (2003).
   Google Scholar
• Rosenbach A, Ram R. Treatment of Acanthosis nigricans of the axillae using a long-pulsed (5-msec) alexandrite laser. Dermatol. Surg.30(8), 1158–1160 (2004).
   PubMed Web of Science ®Google Scholar
• Mishriki YY. Skin commotion from repetitive devotion. Prayer callus. Postgrad. Med.105, 153 (1999).
   PubMed Web of Science ®Google Scholar
• Kahana M, Cohen M, Ronnen M et al. Prayer nodules in Moslem men. Cutis38(4), 281–282 (1986).
   Google Scholar
• Cress RD, Holly EA. Incidence of cutaneous melanoma among non-Latino whites, Latinos, Asians, and blacks: an analysis of California cancer registry data, 1988–1993. Cancer Causes Control8, 246 (1997).
   PubMedGoogle Scholar
• Hu S, Soza-Vento RM, Parker DF et al. Comparison of stage at diagnosis of melanoma among Hispanic, black, and white patients in Miami-Dade County, Florida. Arch. Dermatol.142, 704 (2006).
   PubMedGoogle Scholar
• Black WC, Goldhahn RT, Wiggins C. Melanoma within a southwestern Latino population. Arch. Dermatol.123, 1331 (1987).
   PubMedGoogle Scholar
• Piptone M, Robinson JK, Camara C et al. Skin cancer awareness in suburban employees: a Latino perspective. J. Am. Acad. Dermatol.47, 118–123 (2002).
   Google Scholar
• Hoegh HJ, Davis BD, Manthe AF. Sun avoidance practices among non-Latino white Californians. Health Edu. Behavior26, 360 (1999).
   PubMed Web of Science ®Google Scholar
• Friedman LC, Bruce S, Weinberg AD et al. Early detection of skin cancer: racial/ethnic differences in behaviors and attitudes. J. Cancer Edu.9, 105 (1994).
   PubMedGoogle Scholar
• Eide MJ, Weinstock MA. Association of UV index, latitude, and melanoma incidence in nonwhite populations – US Surveillance, Epidemiology, and End Results (SEER) program, 1992 to 2001. Arch. Dermatol.141, 477–481 (2005).
   PubMed Web of Science ®Google Scholar
• Hu S, Ma F, Collado-Mesa F et al. UV Radiation, latitude, and melanoma in US Latinos and Blacks. Arch Dermatol.140, 819–824 (2004).
   PubMedGoogle Scholar
• Hoy WE. Nonmelanoma skin carcinoma in Albuquerque, New Mexico: experience of a major health care provider. Cancer77, 2489–2495 (1996).
   Google Scholar
• Harris RB, Griffith K, Moon TE. Trends in the incidence of nonmelanoma skin cancers in southeastern Arizona, 1985–1996. J. Am. Acad. Dermatol.45, 528 (2001).
   PubMed Web of Science ®Google Scholar
• Zemelman V, von Beck P, Alvarado O et al. Sexual dimorphism in skin eye and hair color and the presence of freckles in Chilean teenagers from two socioeconomic strata. Revista Medica de Chile130, 879 (2002).
   PubMed Web of Science ®Google Scholar
• Bigler C, Feldman J, Hall E et al. Pigmented basal cell carcinoma in Latinos. J. Am. Acad. Dermatol.34, 751 (1996).
   PubMed Web of Science ®Google Scholar
• Abarca JF, Casiccia CC. Skin cancer and ultraviolet-B radiation under the Antarctic ozone hole: southern Chile, 1987–2000. Photoderm. Photoimmunol. Photomed.18, 294 (2002).
   PubMed Web of Science ®Google Scholar
• Calderon-Garciduenas L, Delgado R, Calderon-Garciduenas A et al. Malignant neoplasms of the nasal cavity and paranasal sinuses: a series of 256 patients in Mexico City and Monterrey. Is air pollution the missing link? Otolaryngol. Head Neck Surg.122(4), 499–508 (2000).
   PubMed Web of Science ®Google Scholar
• Hurtig AK, San Sebastain M. Geographical differences in cancer incidence in the Amazon basin of Ecuador in relation to residence near oil fields. Int. J. Epidemiol.31, 1021 (2002).
   PubMed Web of Science ®Google Scholar
• Grinspan D, Bianini R. Chronic endemic regional hydroarsenicism. The manifestations of arsenic poisoning caused by drinking water. Medicina Cutanea Ibero-Latino-Americana13, 85 (1985).
   Google Scholar