Saha Priyanka, Rachapalli Keerthika Reddy, Bhat B Rajeshwari, Ansari Waqar Ahmed, Ansari Asif, Desai Hridayanath
Department of General Surgery, Grant Government Medical College and Sir J&J Group of Hospitals, Mumbai, India.
Department of General Surgery, Grant Government Medical College and Sir J&J Group of Hospitals, Mumbai, India.
Int J Surg Case Rep. 2021 Jun;83:106043. doi: 10.1016/j.ijscr.2021.106043. Epub 2021 May 26.
The origin of the mesenteric vasculature is highly variable. One such variation is the common celiaco-mesenteric trunk (CMT). To our knowledge, this is the first reported case of subacute duodenal obstruction caused by common CMT. The awareness of this anomaly helps keep a high index of suspicion for varied presentations, prompts appropriate investigations, timely intervention, and avoids iatrogenic injury.
A 15-year-old boy presented with a history of repeated attacks of colicky abdominal pain with bilious vomiting. Computed tomography of the abdomen with intravenous contrast revealed subacute duodenal obstruction caused by an acute angulation of common CMT with the abdominal aorta. To relieve the obstruction, the patient underwent a side-to-side duodenojejunostomy.
A common CMT, where the coeliac artery (CA) and superior mesenteric artery (SMA) have a common origin from the aorta, accounts for less than 1% of all splanchnic artery anomalies. Most CMTs are incidental findings, but aneurysm or dissection of the common trunk commonly accompany this anatomical aberrancy. Intestinal obstruction due to CMT anomaly is a rare occurrence.
There should be a high index of suspicion concerning vascular anomalies in patients, especially children presenting with repeated episodes of subacute intestinal obstruction. This knowledge of vascular aberrations prevents disastrous iatrogenic complications.
肠系膜血管的起源高度可变。其中一种变异是腹腔干-肠系膜上动脉共干(CMT)。据我们所知,这是首例由CMT导致的亚急性十二指肠梗阻的报告病例。认识到这种异常有助于对各种表现保持高度怀疑指数,促使进行适当的检查、及时干预并避免医源性损伤。
一名15岁男孩,有反复发作的绞痛性腹痛伴胆汁性呕吐病史。腹部增强CT显示,CMT与腹主动脉急性成角导致亚急性十二指肠梗阻。为缓解梗阻,患者接受了十二指肠空肠侧侧吻合术。
CMT是指腹腔干(CA)和肠系膜上动脉(SMA)从主动脉共同起源,占所有内脏动脉异常的比例不到1%。大多数CMT是偶然发现,但共同干的动脉瘤或夹层通常伴随这种解剖变异。CMT异常导致的肠梗阻很少见。
对于反复出现亚急性肠梗阻发作的患者,尤其是儿童,应高度怀疑血管异常。了解血管变异可预防灾难性的医源性并发症。