反复腹水超出通常的怀疑:发现一个被忽视的罪魁祸首。

Case Reports in Hepatology Pub Date : 2025-05-24 eCollection Date: 2025-01-01 DOI:10.1155/crhe/9961539
Binoy Desai, Harjit Singh, Alessandra Martorella, Bryce Kunkle, Amol S Rangnekar
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引用次数: 0

摘要

肝淀粉样变是一种罕见的导致进行性肝功能障碍的疾病。诊断通常具有挑战性,因为临床表现可能多种多样,并取决于肝脏受累程度、淀粉样蛋白沉积的潜在病因以及伴随的肝外表现。腹水,虽然不常见,但可能是肝淀粉样变的一个表现特征,并提出诊断挑战,因为它可以发生在各种肝脏和非肝脏相关疾病。在此,我们报告一例复发性腹水患者的肝淀粉样变,强调在鉴别诊断中考虑这种情况的重要性,这些个体呈现不明原因的腹水。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recurrent Ascites Beyond the Usual Suspects: Uncovering an Overlooked Culprit.

Hepatic amyloidosis is a rare condition that leads to progressive liver dysfunction. Diagnosis is often challenging since clinical presentation may be highly varied and is dependent upon the extent of liver involvement, underlying etiology of amyloid deposition, as well as concomitant extrahepatic manifestations. Ascites, although uncommon, can be a presenting feature of hepatic amyloidosis and pose diagnostic challenges as it can occur in a variety of liver and nonliver-related conditions. Herein, we present a case of hepatic amyloidosis in a patient with recurrent ascites, emphasizing the importance of considering this condition in the differential diagnosis of individuals presenting with unexplained ascites.

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