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遗传性出血性毛细血管扩张症继发胆道出血所致胆管炎和充血性心力衰竭

Cholangitis and Congestive Heart Failure Secondary to Biliary Hemorrhage in Hereditary Hemorrhagic Telangiectasia.

作者信息

Yamamoto Hiroki, Kimura Masamichi, Otoyama Yumi, Imamura Jun, Kimura Kiminori

机构信息

Hepatology, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, JPN.

出版信息

Cureus. 2024 Dec 6;16(12):e75232. doi: 10.7759/cureus.75232. eCollection 2024 Dec.

Abstract

This case report discusses the case of a 74-year-old man who was diagnosed with hereditary hemorrhagic telangiectasia (HHT). The patient initially presented with right upper quadrant abdominal pain and was later diagnosed with cholangitis. Subsequently, heart failure was identified due to hepatic arteriovenous malformations. Although the exact duration of his disease remains unclear, the patient was initially asymptomatic and developed significant complications over time, possibly reflecting the progressive nature of vascular malformations associated with HHT. This case underscores the necessity of regular imaging follow-ups to assess the progression of vascular malformations in various organs, highlighting the clinical significance of the early detection and management of complications in HHT.

摘要

本病例报告讨论了一名74岁男性被诊断为遗传性出血性毛细血管扩张症(HHT)的病例。患者最初表现为右上腹腹痛,随后被诊断为胆管炎。随后,因肝动静脉畸形确诊心力衰竭。尽管其疾病的确切病程尚不清楚,但患者最初无症状,随着时间推移出现了严重并发症,这可能反映了与HHT相关的血管畸形的进展性。该病例强调了定期进行影像学随访以评估各器官血管畸形进展的必要性,突出了HHT并发症早期检测和管理的临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74f4/11700518/5729d5992783/cureus-0016-00000075232-i01.jpg

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