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自发性十二指肠壁内血肿伴短暂性胆道梗阻和急性胆囊炎。

Spontaneous intramural duodenal haematoma with transient biliary obstruction and acute cholecystitis.

机构信息

Gastroenterology Unit, Department of Medicine, Raja Isteri Pengiran Anak Saleha Hospital, Bandar Seri, Begawan, BA 1710 Brunei Darussalam.

出版信息

Singapore Med J. 2010 Dec;51(12):e198-200.

Abstract

Intramural duodenal haematoma (IDH) is uncommon and usually presents with upper gastrointestinal bleeding. Trauma, anticoagulant therapy, blood coagulation disorders and endoscopic interventions have been reported to cause IDH. IDH secondary to antiplatelet therapy has not been previously reported in the literature. We report IDH secondary to aspirin therapy that was associated with transient obstructive jaundice and acute cholecystitis in a 47-year-old woman. The patient was successfully managed with conservative management.

摘要

肠壁内十二指肠血肿(IDH)较为少见,通常表现为上消化道出血。创伤、抗凝治疗、血液凝血障碍和内镜介入已被报道可导致 IDH。在文献中,先前未有报道过 IDH 继发于抗血小板治疗。我们报告了一例 47 岁女性,因阿司匹林治疗导致 IDH,同时伴有短暂性梗阻性黄疸和急性胆囊炎。该患者经保守治疗成功治愈。

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