98
Views
0
CrossRef citations to date
0
Altmetric
Case Report

Pseudo-Meigs’ Syndrome in Tunisian H Syndrome Female Patient: First Case Reported

, ORCID Icon, , , , , , & show all
Pages 235-239 | Published online: 15 Apr 2021

References

  • Molho-Pessach V, Agha Z, Aamar S, et al. The H syndrome: a genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations. J Am Acad Dermatol. 2008;59(1):79‑85. doi:10.1016/j.jaad.2008.03.021
  • Molho-Pessach V, Lerer I, Abeliovich D, et al. The H syndrome is caused by mutations in the nucleoside transporter hENT3. Am J Hum Genet. 2008;83(4):529‑34. doi:10.1016/j.ajhg.2008.09.013
  • Molho-Pessach V, Ramot Y, Camille F, et al. H syndrome: the first 79 patients. J Am Acad Dermatol. 2014;70(1):80–8. doi:10.1016/j.jaad.2013.09.019
  • Bhatti S, Jamil A, Siddiqui SH, Yaqoob U, Virk LN, Bhatti A. The H Syndrome: a genodermatosis. Cureus. 2018;10(6):e2763.
  • Spiegel R, Cliffe ST, Buckley MF, et al. Expanding the clinical spectrum of SLC29A3 gene defects. Eur J Med Genet. 2010;53(5):309‑13. doi:10.1016/j.ejmg.2010.06.012
  • Emile J-F, Abla O, Fraitag S, et al. Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages. Blood. 2016;127(22):2672‑81. doi:10.1182/blood-2016-01-690636
  • Doviner V, Maly A, Ne’eman Z, et al. H syndrome: recently defined genodermatosis with distinct histologic features. A morphological, histochemical, immunohistochemical, and ultrastructural study of 10 cases. Am J Dermatopathol. 2010;32(2):118‑28. doi:10.1097/DAD.0b013e3181b28572
  • El-Bassyouni HT, Thomas MM, Tosson AMS. Mutation in the SLC29A3 Gene in an Egyptian patient with H syndrome: a case report and review of literature. J Pediatr Genet. 2020;9(2):109‑13. doi:10.1055/s-0039-1697900
  • Rezvani A, Taherifard E, Mokhtari M, Feili A, Movahed H. H syndrome with a possibly new immunological phenotype. Int J Dermatol. 2020;59(7):e248‑51. doi:10.1111/ijd.14867
  • David O, Geylis M, Kristal E, Ling G, Schreiber R. Glomerular involvement in children with H syndrome. Pediatr Nephrol Berl Ger. 2021;36(3):721‑4.
  • Jaouadi H, Zaouak A, Sellami K, et al. H syndrome: clinical, histological and genetic investigation in Tunisian patients. J Dermatol. 2018;45(8):978‑85. doi:10.1111/1346-8138.14359
  • Meigs JV. Fibroma of the ovary with ascites and hydrothorax; Meigs’ syndrome. Am J Obstet Gynecol. 1954;67(5):962‑85. doi:10.1016/0002-9378(54)90258-6
  • Daoudi M, Herrak L, Ftouh ME, Achachi L. Pseudo-Meigs syndrome secondary to ovarian serous cystadenoma. Pan Afr Med J. 2019;33:11. doi:10.11604/pamj.2019.33.11.18128
  • Benjapibal M, Sangkarat S, Laiwejpithaya S, Viriyapak B, Chaopotong P, Jaishuen A. Meigs’ syndrome with elevated serum CA125: case report and review of the literature. Case Rep Oncol. 2009;2(1):61‑6. doi:10.1159/000210441
  • Shiau C-S, Chang M-Y, Hsieh -C-C, Hsieh -T-T, Chiang C-H. Meigs’ syndrome in a young woman with a normal serum CA-125 level. Chang Gung Med J. 2005;28(8):587‑91.