Atri Souhaib, Debiche Ahmed, Sebai Amine, Eya Azouz, Haddad Anis, Kacem Montassar
Hopital la Rabta, Tunis, Tunisia; University of Tunis El Manar Faculty of Medicine of Tunis.
Hopital la Rabta, Tunis, Tunisia; University of Tunis El Manar Faculty of Medicine of Tunis.
Int J Surg Case Rep. 2024 Mar;116:109395. doi: 10.1016/j.ijscr.2024.109395. Epub 2024 Feb 16.
Acute intestinal intussusception (AII) in adults, unlike in children, is a rare manifestation that is frequently secondary to malignant or benign tumors and intestinal intussusception on a lipoma is more exceptional.
We present a rare case of AII caused by a lipoma in a previously healthy 44-year-old man. He experienced severe right lower quadrant pain and constipation. An abdominal CT scan revealed ileocecal intussusception, displaying the classic "sandwich" and "cocarde" images. Additionally, a Caecal lipoma was identified. The patient underwent midline laparotomy, revealing significant small bowel distention upstream of the ileocolic intussusception. Subsequently, a right hemicolectomy with ileocolostomy was performed. Pathological examination confirmed colonic ischemic necrosis attributed to AII originating from a submucosal caecal lipoma.
AII is a rare cause of abdominal pain and accounts for 1 to 5 % of adult intestinal obstructions. In adults, an organic cause is found in 70 to 90 % of cases, often secondary to an endoluminal lesion of malignant nature. Pure colonic intussusception on a lipoma is exceptional. CT scan, can show characteristic images and confirms the fatty nature of the lipoma. Surgical intervention is necessary as treatment for intussusception and anatomopathological examination is required for diagnostic confirmation.
Intestinal intussusception caused by an intestinal lipoma is rare. Imaging, mainly ultrasound and CT scan, plays a crucial role in providing a positive and etiological diagnosis of the condition by showing characteristic images. Treatment is always surgical, and there is no place for reduction under radiological control.
与儿童不同,成人急性肠套叠(AII)是一种罕见的表现,常继发于恶性或良性肿瘤,而脂肪瘤引起的肠套叠更为罕见。
我们报告一例罕见的AII病例,发生在一名44岁既往健康的男性身上,由脂肪瘤引起。他经历了严重的右下腹疼痛和便秘。腹部CT扫描显示回盲部肠套叠,呈现出典型的“三明治”和“徽章”图像。此外,还发现了盲肠脂肪瘤。患者接受了正中剖腹手术,发现回结肠套叠上游的小肠明显扩张。随后,进行了右半结肠切除术并做了回结肠造口术。病理检查证实了由盲肠黏膜下脂肪瘤引起的AII导致的结肠缺血性坏死。
AII是腹痛的罕见原因,占成人肠梗阻的1%至5%。在成人中,70%至90%的病例可发现器质性病因,通常继发于恶性性质的腔内病变。脂肪瘤导致的单纯结肠套叠非常罕见。CT扫描可以显示特征性图像并证实脂肪瘤的脂肪性质。手术干预是治疗肠套叠的必要手段,诊断确认需要进行解剖病理学检查。
肠脂肪瘤引起的肠套叠很罕见。影像学检查,主要是超声和CT扫描,通过显示特征性图像在对该病进行阳性和病因诊断方面起着关键作用。治疗始终是手术治疗,不适合在放射控制下进行复位。