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表现为急腹症的孤立性肠系膜血管异常

Solitary mesenteric vascular anomaly presenting as acute abdomen.

作者信息

Thambidorai C R, Wahab A, Hamzaini A H

机构信息

Paediatric Surgery Unit, Departments of Surgery and Radiology, University Kebangsaan of Malaysia, Cheras, 56000 Kuala Lumpur, Malaysia.

出版信息

J Indian Assoc Pediatr Surg. 2008 Jul;13(3):115-7. doi: 10.4103/0971-9261.43820.

Abstract

A 4-year-old girl with a solitary vascular anomaly of the mesentery presented with acute lower abdominal pain. Despite the use of ultrasound, computed tomography scan and image-guided core biopsies, the lesion was initially mistaken for an inflammatory intra-abdominal mass. The correct diagnosis was made at laparotomy. Solitary vascular anomaly of the mesentery is rare and its presentation as an acute abdomen has not been reported before.

摘要

一名患有肠系膜孤立性血管异常的4岁女孩出现急性下腹痛。尽管使用了超声、计算机断层扫描和图像引导下的核心活检,但该病变最初被误诊为腹腔内炎性肿块。剖腹手术时做出了正确诊断。肠系膜孤立性血管异常罕见,此前尚无其表现为急腹症的报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c15/2788461/24a43a7438a0/JIAPS-13-115-g001.jpg

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