慢性腹痛和Budd-Chiari综合征:对潜在肿瘤病因的不懈探索。

Canadian liver journal Pub Date : 2022-08-16 eCollection Date: 2022-08-01 DOI:10.3138/canlivj-2021-0039
Natasha Chandok, Said Ishmail, Jeffrey Jaskolka, Sanjeev Sirpal
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引用次数: 0

摘要

在这篇文章中,我们报告了一位62岁的非肝硬化男性,因慢性腹痛、厌食症和体重减轻而就诊于急诊科。初次就诊时,体格检查无明显异常,除了肌肉减少和脾肿大。最初的影像学检查显示从髂静脉到右心房有一个很大的血栓形成。出院后4个月,患者再次到急诊科就诊,因肾功能衰竭和腹水再次入院。确定Budd-Chiari综合征(BCS)的诊断。免疫组化阳性证实为上皮性质的肿瘤形态。该病例为继发性BCS的临床表现提供了一个独特的视角,需要考虑血管旁原因的鉴别诊断。在这种情况下,慢性腹痛,往往被忽视,可能需要进一步的检查,以建立临床诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chronic abdominal pain and Budd-Chiari syndrome: A relentless quest for an underlying neoplastic etiology.

In this article, we report on a 62-year-old non-cirrhotic male presenting to the emergency department (ED) with chronic abdominal pain, anorexia, and weight loss. Upon initial presentation, physical exam was unremarkable, other than for sarcopenia and splenomegaly. Initial imaging studies revealed a large thrombosis from the iliac vein to the right atrium of the heart. Following discharge, the patient re-consulted to the ED four months later and was re-admitted in renal failure and ascites. The diagnosis of Budd-Chiari syndrome (BCS) was established. Positive immunohistochemistry confirmed a neoplastic ideology of epithelial nature. This case offers a unique perspective on the clinical presentation of secondary BCS, necessitating a consideration in the differential diagnosis of a para-vascular cause. In this case, chronic abdominal pain, often overlooked, may necessitate further workup to establish a clinical diagnosis.

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