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布加综合征继发于真性红细胞增多症。病例报告。

Budd-Chiari syndrome secondary to polycythemia vera. A case report.

机构信息

Third Medical Clinic, Radiology Department, University of Medicine and Pharmacy, Croitorilor Str., 19-21, Cluj-Napoca, Romania.

出版信息

J Gastrointestin Liver Dis. 2009 Sep;18(3):363-6.

Abstract

Budd-Chiari syndrome still represents a challenge for the hepatologist with regard to its causes and its most effective therapy. Polycythemia vera is considered to be the most frequent condition causing the Budd-Chiari syndrome (10-40% of cases). We present a 34-year-old patient in post-partum who was admitted for right upper abdominal quadrant pain and asthenia. Laboratory data, abdominal echography and angioMRI all raised the suspicion of BCS, but it was in the haematological department that polycytemia vera was diagnosed as the cause of the hepatic condition.

摘要

布加综合征仍然是肝病学家在病因和最有效治疗方面面临的挑战。真性红细胞增多症被认为是导致布加综合征的最常见疾病(占 10-40%的病例)。我们报告了一位 34 岁的产后患者,因右上腹疼痛和乏力入院。实验室数据、腹部超声和血管 MRI 均提示布加综合征,但在血液科诊断为真性红细胞增多症,导致了肝脏疾病。

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