遗传性血管性水肿II型:首次表现为成年期复发性严重腹痛。

Pub Date : 2018-10-29 eCollection Date: 2018-01-01 DOI:10.1155/2018/7435870
Mohamed Abuzakouk, Nada AlMahmeed, Esat Memisoglu, Martine McManus, Aydamir Alrakawi
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引用次数: 6

摘要

一名27岁的阿联酋男子,因身体不同部位反复出现严重肿胀4年,来到阿布扎比克利夫兰诊所急诊科就诊。他以前每周有2次肿胀发作,影响他的脸、手、脚或阴囊,每周有两次严重的腹痛。腹部CT扫描和结肠镜检查显示肠壁水肿。没有类似的家族史或遗传性血管性水肿(HAE)。补体研究证实了HAE II型的诊断。患者开始服用达那唑100 mg,每日2次,症状消失。本病例报告强调了在没有HAE家族史的复发性不明原因腹痛患者中考虑HAE的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hereditary Angioedema Type II: First Presentation in Adulthood with Recurrent Severe Abdominal Pain.

Hereditary Angioedema Type II: First Presentation in Adulthood with Recurrent Severe Abdominal Pain.

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Hereditary Angioedema Type II: First Presentation in Adulthood with Recurrent Severe Abdominal Pain.

A 27-year-old Emirate man presented to Cleveland Clinic Abu Dhabi emergency department with a 4 year history of recurrent episodes of severe swellings affecting different parts of his body. He used to get 2 swelling episodes every week affecting either his face, hands, feet or scrotum and severe abdominal pain twice a week. Abdominal CT scan and a colonoscopy showed bowel wall oedema. There was no family history of similar complaint or of hereditary angioedema (HAE). Complement studies confirmed the diagnosis of HAE type II. He was commenced on danazol 100 mg twice daily and his symptoms resolved. This case report highlights the importance of considering HAE in patients with recurrent unexplained abdominal pain even in the absence of positive family history of HAE.

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