Thambidorai C R, Wahab A, Hamzaini A H
Paediatric Surgery Unit, Departments of Surgery and Radiology, University Kebangsaan of Malaysia, Cheras, 56000 Kuala Lumpur, Malaysia.
J Indian Assoc Pediatr Surg. 2008 Jul;13(3):115-7. doi: 10.4103/0971-9261.43820.
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.
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。
