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与胰腺炎相关的胆管自发性破裂。一种罕见的表现。

Spontaneous rupture of the bile duct associated with pancreatitis. A rare presentation.

作者信息

Goenka Mahesh K, Acharyya Bhaswati C, Sethy Pradeepta K, Goenka Usha

机构信息

Institute of Gastroenterology, Apollo Gleneagles Hospital. Kolkata, India.

出版信息

JOP. 2011 Mar 9;12(2):149-51.

Abstract

CONTEXT

Spontaneous rupture of the bile duct, although rare, has been described as a known surgical cause of jaundice in infancy after biliary atresia.

CASE REPORT

This article describes a four-year-old girl who presented with severe abdominal pain and features suggestive of acute pancreatitis, who developed gradual distension of the abdomen, and was found to have a ruptured bile duct, producing biliary peritonitis. She was managed with laparoscopic drainage of the peritoneal cavity. However, in view of the persistent biliary drainage, an ERCP was performed followed by stent placement for a bile duct leak. She was subsequently diagnosed as having a choledochal cyst.

CONCLUSION

A high index of suspicion, appropriate investigation, such as MRCP, combined with early drainage can help in reaching an early diagnosis, and reduced morbidity and mortality in this rare disorder.

摘要

背景

胆管自发性破裂虽罕见,但已被描述为婴儿期胆道闭锁后黄疸的一种已知外科病因。

病例报告

本文描述了一名4岁女孩,她出现严重腹痛及提示急性胰腺炎的特征,随后腹部逐渐膨隆,被发现有胆管破裂,导致胆汁性腹膜炎。她接受了腹腔镜下腹腔引流治疗。然而,鉴于持续的胆汁引流,进行了内镜逆行胰胆管造影(ERCP),随后放置胆管支架以治疗胆管渗漏。她随后被诊断为胆总管囊肿。

结论

高度的怀疑指数、适当的检查(如磁共振胰胆管造影(MRCP))以及早期引流有助于早期诊断,并降低这种罕见疾病的发病率和死亡率。

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