Ayadi Taha Yassine, Behi Hager, Guelmami Hanene, Changuel Amel, Tlili Karima, Khalifa Mohamed Bachir
General Surgery Department, Military Hospital of Tunis, Mont Fleury-1008, Tunis, Tunisia; Faculty of Medicine of Tunis, 15, Djebel Lakhdhar Street - 1007 Bab Saadoun, Tunis, Tunisia.
General Surgery Department, Military Hospital of Tunis, Mont Fleury-1008, Tunis, Tunisia; Faculty of Medicine of Tunis, 15, Djebel Lakhdhar Street - 1007 Bab Saadoun, Tunis, Tunisia.
Int J Surg Case Rep. 2024 Aug;121:109920. doi: 10.1016/j.ijscr.2024.109920. Epub 2024 Jun 20.
Intestinal intussusception is a rare complication in adults, accounting for 1 % of intestinal obstructions. Unlike in children, it is often secondary to a malignant lesion, rarely a benign one. Colonic lipomas are asymptomatic benign tumors often discovered incidentally. Colo-colonic intussusception due to a lipoma is exceptional. Here, we report a rare case of colo-colonic intussusception secondary to a giant caecal lipoma occurring in a 65-year-old woman.
A 65-year-old woman, was admitted in our surgical department for intermittent crampy abdominal pain in the right iliac fossa with an alternation of diarrhea and constipation over the past 10 months. The radiological investigation revealed a colo-colonic intussusception, most likely secondary to a fatty mass in the cecum. A right hemicolectomy was performed with ileocolic anastomosis because of the risk of malignancy. Histopathological examination confirmed the lipomatous nature of the lesion. The patient remained asymptomatic three years after surgery.
Colonic lipomas are often asymptomatic. They can cause intussusception with clinical symptoms varying based on their size and location. CT scan has increased the number of preoperative diagnoses. Treatment options include surveillance, endoscopic intervention, or surgical resection. The appropriate surgical intervention remains a major challenge for surgeons due to the risk of malignancy.
A giant colonic lipoma remains a very rare cause of colonic intussusception, especially in adults. CT scan plays a crucial role in diagnosis. Surgical resection remains the treatment of choice due to the risk of malignancy.
成人肠套叠是一种罕见的并发症,占肠梗阻的1%。与儿童不同,它通常继发于恶性病变,很少继发于良性病变。结肠脂肪瘤是无症状的良性肿瘤,常为偶然发现。脂肪瘤导致的结肠-结肠套叠极为罕见。在此,我们报告一例65岁女性因巨大盲肠脂肪瘤继发结肠-结肠套叠的罕见病例。
一名65岁女性因右下腹间歇性绞痛伴腹泻与便秘交替发作10个月入住我院外科。影像学检查显示为结肠-结肠套叠,极有可能继发于盲肠的一个脂肪性肿物。因存在恶变风险,遂行右半结肠切除术并作回结肠吻合术。组织病理学检查证实了病变的脂肪瘤性质。术后三年患者仍无症状。
结肠脂肪瘤通常无症状。它们可导致套叠,临床症状因大小和位置而异。CT扫描增加了术前诊断的数量。治疗选择包括监测、内镜干预或手术切除。由于存在恶变风险,合适的手术干预对外科医生来说仍是一项重大挑战。
巨大结肠脂肪瘤仍然是结肠套叠的一种非常罕见的病因,尤其是在成人中。CT扫描在诊断中起着关键作用。由于存在恶变风险,手术切除仍是首选治疗方法。