Article Sidebar

Download
PDF (Français) Sans titre (Français) Sans titre (Français)

Main Article Content

Abstract

La maladie de Rendu-Osler-Weber est une affection rare, de transmission autosomique dominante, d’expression variable, jamais décrite au Gabon. Le diagnostic exige la présence d'au moins trois sur quatre critères cliniques de Curaçao. Nous rapportons un cas à atteinte hépatique révélé sous la forme d’une hépatomégalie pseudo-tumorale.

Article Details

How to Cite
Itoudi Bignoumba, P. E., Maganga Moussavou, I., Eyi Nguema, A. G., Mbounja Zue, M., Nzouto, P. D., Saibou, M., & Moussavou Kombila, J. B. (2020). La Maladie de Rendu Osler Weber Révélée par une Hépatomégalie Douloureuse. HEALTH SCIENCES AND DISEASE, 21(2). https://doi.org/10.5281/hsd.v21i2.1825
Download Citation
Endnote/Zotero/Mendeley (RIS)
BibTeX

References

  1. Tortora A, Riccioni ME, Gaetani E, Ojetti V, Holleran G, Gasbarrini A. Rendu-Osler-Weber disease: a gastroenterologist's perspective. Orphanet J Rare Dis. 2019, 7;14(1):130. doi: 10.1186/s13023-019-1107-4.
  2. Boehlen F, landis BN, spahr L et al. Maladie de Rendu-Osler-Weber : importance d’une prise en charge multidisciplinaire. Rev Med Suisse 2016 ; 12 : 1056-62
  3. Dupuis-Girod S, Bailly S, Plauchu H. Hereditary hemorrhagic telangiectasia : from molecular biology to patient care. J Thromb Haemost 2010;8:1447-56.
  4. Garcia-Tsao G. Liver involvement in hereditary hemorrhagic telangiectasia. J Hepatol 2007;46:499-507.
  5. Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 2000;91:66-7.
  6. Geisthoff UW, Nguyen HL, Röth A, Seyfert U. How to manage patients with hereditary haemorrhagic telangiectasia. Br J Haematol 2015;171:443-52.
  7. D upuis-Girod S, Chesnais AL, Ginon I, et al. Long-term outcome of patients with hereditary hemorrhagic telangiectasia and severe hepatic involvement after orthotopic liver transplantation : A single-center study. Liver Transpl 2010;16:340-7.
  8. Welle CL, Welch BT, Brinjikji W, et al. Abdominal manifestations of hereditary hemorrhagic telangiectasia: a series of 333 patients over 15 years. Cureus. 2018 Sep 14;10(9):e3305. doi: 10.7759/cureus.3305
  9. Kiyeng JC, Siika A, Koech C, Bloomfield GS. Definite hereditary hemorrhagic telangiectasia in a 60-year-old black Kenyan woman: a case report. J Med Case Rep. 2016 May 25;10(1):126. doi: 10.1186/s13256-016-0909-4.
  10. Ljaz HM, Lodhi MU, Chowdhury W, et al. Co-existing Gastrointestinal Hemorrhage and Deep Vein Thrombosis in a Patient with Hereditary Hemorrhagic Telangiectasia: Management Dilemma.. 2019 Jul;44(7):2384-2391. doi: 10.1007/s00261-019-01976-7.

Most read articles by the same author(s)