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腹部遗传性血管性水肿的磁共振成像表现。

Abdominal hereditary angio-oedema caught on magnetic resonance imaging.

机构信息

General Medicine, Maidstone and Tunbridge Wells NHS Trust, Tunbridge Wells, UK

General Medicine, Maidstone and Tunbridge Wells NHS Trust, Tunbridge Wells, UK.

出版信息

BMJ Case Rep. 2021 Dec 31;14(12):e246339. doi: 10.1136/bcr-2021-246339.

Abstract

A 17-year-old woman presented with a 3-year history of recurrent, severe abdominal pain with spontaneous resolution within a few days. An ultrasound revealed nothing more than free fluid within the pelvis. An MRI of the small bowel was done within 24 hours of abdominal pain onset, which revealed extensive submucosal oedema associated with moderate volume ascites. A repeat MRI of the small bowel after 72 hours showed near-complete resolution of these changes. Checking C1 inhibitor levels confirmed a diagnosis of hereditary angio-oedema with an abdominal presentation. This is a rare cause of recurrent abdominal pain and, to our knowledge, the first case in which MR images have been obtained during and after an acute attack.

摘要

一位 17 岁女性因反复发作的严重腹痛就诊,腹痛在数天内自行缓解。超声检查除盆腔内有游离液体外无其他异常。腹痛发作后 24 小时内行小肠 MRI 检查,结果显示广泛的黏膜下水肿,伴有中等量腹水。腹痛发作后 72 小时再次行小肠 MRI 检查,显示这些改变几乎完全消退。检查 C1 抑制剂水平后确诊为遗传性血管性水肿伴腹部表现。这是一种罕见的复发性腹痛病因,据我们所知,这是首例在急性发作期间和之后获得 MRI 图像的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68e/8720948/da632a996f0d/bcr-2021-246339f01.jpg

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