Bathobakae Lefika, Ansari Nida, Mahmoud Anas, Hasan Shayee, Yuridullah Ruhin, Qayyum Sohail, Rae Sam
Internal Medicine, St. Joseph's University Medical Center, Paterson, USA.
Gastroenterology and Hepatology, St. Joseph's University Medical Center, Paterson, USA.
Case Rep Gastrointest Med. 2024 Jan 23;2024:6679725. doi: 10.1155/2024/6679725. eCollection 2024.
Familial Mediterranean fever (FMF) is a hereditary disorder characterized by episodes of fever, polyserositis, or cutaneous inflammation. The FMF attacks last 1-3 days and have no apparent triggers. Recurrent deposition of the serum amyloid A (SAA) protein in the gut can cause intractable diarrhea, dysmotility, and recurrent abdominal pain. Gastrointestinal amyloidosis is a rare, but serious, complication of FMF. In this case report, we describe a rare case of chronic diarrhea and recurrent abdominal pain due to FMF-induced gastrointestinal amyloidosis.
家族性地中海热(FMF)是一种遗传性疾病,其特征为发热、多浆膜炎或皮肤炎症发作。FMF发作持续1 - 3天,且无明显诱因。血清淀粉样蛋白A(SAA)在肠道反复沉积可导致顽固性腹泻、动力障碍和反复腹痛。胃肠道淀粉样变性是FMF一种罕见但严重的并发症。在本病例报告中,我们描述了一例因FMF引起的胃肠道淀粉样变性导致慢性腹泻和反复腹痛的罕见病例。