| Literature DB >> 16733390 |
Antoine de Leusse1, Evelyne Dupuy, Marjan Huizing, Claire Danel, Guy Meyer, Raymond Jian, Philippe Marteau.
Abstract
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder characterized by oculocutaneous albinism and platelet dysfunction. A subset of patients also show ceroid deposition, which can result in pulmonary fibrosis or granulomatous colitis. Whether this colitis may be considered Crohn's disease is under debate. We report a case of a patient with HPS associated with inflammatory bowel disease which affected the distal small bowel but not the colon. Ileitis was severe, and recurred rapidly after surgery. Search for mutations in HPS1, ADTB3A, HPS3, HPS4 and for CARD15 were negative. Symptoms and ileal ulcerations which recurred after surgery were successfully treated with azathioprine and infliximab.Entities:
Mesh:
Year: 2006 PMID: 16733390 DOI: 10.1016/s0399-8320(06)73239-0
Source DB: PubMed Journal: Gastroenterol Clin Biol ISSN: 0399-8320