Jha Rahul, Bhatta Bijay Raj, Shrestha Alina, Shrestha Anish, Dahal Mridul, Maharjan Seejana Singh
Department of General Surgery, National Academy of Medical Sciences, Kathmandu, Nepal.
Department of General Surgery, National Academy of Medical Sciences, Kathmandu, Nepal.
Int J Surg Case Rep. 2025 Jul;132:111452. doi: 10.1016/j.ijscr.2025.111452. Epub 2025 May 19.
Appendicular band syndrome is an extremely rare surgical emergency, and only a few cases have been reported in the literature. Although intestinal obstruction comprises 2 % - 8 % of the cases of acute abdomen presenting to emergency, obstruction due to appendicular band syndrome is a rare entity.
A 43-year-old male presented with features suggestive of small bowel obstruction for 5 days. On examination, the abdomen was distended and tense with generalized mild tenderness all over the abdomen. CECT (abdomen and pelvis) showed a transition point in the distal ileum, with dilated bowel loops proximal to it. On exploratory laparotomy, the appendix was found completely encircling the distal ileum, forming a constricting band, for which release of appendicular band with appendectomy was done.
The initiating event in appendicular band syndrome is acute appendicitis itself. Due to the inflammation of appendix, its tip gets adhered to the caecum, retro-peritoneum, ileal mesentery, or ileum itself, forming a potential gap. A segment of bowel may herniate through this gap and become entrapped, resulting in closed-loop obstruction and subsequent strangulation. In the absence of bowel strangulation, releasing the appendicular band along with appendectomy is sufficient. However, if the bowel loop is found to be gangrenous, resection with primary anastomosis is warranted.
Appendicular band syndrome, often diagnosed intraoperatively, should be kept in mind as one of the differential diagnoses when evaluating patients with features of bowel obstruction. Early diagnosis guides incision planning, while timely surgical intervention is crucial for preventing serious complications.
阑尾束带综合征是一种极其罕见的外科急症,文献中仅报道过少数病例。尽管肠梗阻占急诊就诊的急腹症病例的2% - 8%,但由阑尾束带综合征引起的梗阻是一种罕见情况。
一名43岁男性出现提示小肠梗阻的症状达5天。检查时,腹部膨隆且紧张,全腹有轻度压痛。腹部和盆腔CT血管造影(CECT)显示回肠末端有一个移行点,其近端肠袢扩张。在剖腹探查术中,发现阑尾完全环绕回肠末端,形成一条束带,遂行阑尾束带松解及阑尾切除术。
阑尾束带综合征的起始事件是急性阑尾炎本身。由于阑尾炎症,其尖端粘连至盲肠、腹膜后、回肠系膜或回肠本身,形成一个潜在间隙。一段肠管可能通过此间隙疝出并被卡住,导致闭袢性肠梗阻及随后的绞窄。在无肠绞窄的情况下,连同阑尾切除术一起松解阑尾束带就足够了。然而,如果发现肠袢已坏疽,则需要进行切除并一期吻合。
阑尾束带综合征常于术中诊断,在评估有肠梗阻症状的患者时,应将其作为鉴别诊断之一予以考虑。早期诊断指导切口规划,而及时的手术干预对于预防严重并发症至关重要。