Ayandipo O O, Abdurrazzaaq A I, Ogun G O, Adeniji-Sofoluwe A T, Ademola A F, Ogundiran T O
Afr J Med Med Sci. 2015 Mar;44(1):95-9.
Adult colo-colonic intussusception is a rare abnormality and it may pose a diagnostic challenge.
To report two cases of adult colo-colonic intussusception with benign lesion as the lead points.
The Clinical records of the two patients containing the management details were retrieved and reviewed.
The 1st case was a 60 year old man presenting with a year history of recurrent left abdominal pain a two week history of fullness left upper and lower abdomen. Examination showed an 8cm by 6 cm mass in the left hypochondrium continuing with another 16cm by 8 cm mass spanning the left lumbar and left iliac fossa. Abdominal ultrasound scan showed a huge mixed echogenic mass in the central abdomen spanning the left hypochondriac, left lumber and suprapubic regions. He had exploratory laparotomy which revealed cob-cobonic intussusception involving the ascending colon up to sigmoid colon. He had subtotal colectomy done. The lead point was a hamartomatous polyp The 2nd case was a 35 year old man with a two month history of recurrent abdominal pain and haematochezia, a month history change in bowel habit and five day history of abdominal distension. Examination showed distended abdomen with generalised tenderness. There was a firm mass in the left hypochondrium extending to the left iliac fossa. Abdominal ultrasound scan confirm intussusception: Exploratory laparotomy showed perforation of transverse colon at the neck of cob-colonic intussusception involving the distal third of the transverse colon to the rectum. He had extended left hernicolectomy and Devine colostomy done. He died 36 h6urs post operation. The lead point was an inflammatory polyp.
Adult colo-colonic intussusception is an uncommon disease which may not present in a typical feature of intussusception as occur in children thus posing diagnostic dilemma. High index of suspicion with radiological investigation will serve to aid rapid and accurate diagnosis.
成人结肠-结肠套叠是一种罕见的异常情况,可能带来诊断挑战。
报告两例以良性病变为起始点的成人结肠-结肠套叠病例。
检索并回顾了这两名患者包含治疗细节的临床记录。
第一例患者为一名60岁男性,有一年复发性左腹痛病史,左上腹和左下腹饱满感两周。检查发现左季肋部有一个8厘米×6厘米的肿块,延续至另一个16厘米×8厘米的肿块,横跨左腰部和左髂窝。腹部超声扫描显示中腹部有一个巨大的混合回声肿块,横跨左季肋部、左腰部和耻骨上区域。他接受了剖腹探查术,发现结肠-结肠套叠累及升结肠至乙状结肠。他接受了次全结肠切除术。起始点是一个错构瘤性息肉。第二例患者为一名35岁男性,有两个月复发性腹痛和便血病史,一个月排便习惯改变病史,腹胀五天。检查发现腹部膨隆,有弥漫性压痛。左季肋部有一个坚实肿块,延伸至左髂窝。腹部超声扫描证实为套叠:剖腹探查术显示结肠-结肠套叠颈部的横结肠穿孔,累及横结肠远端三分之一至直肠。他接受了扩大的左半结肠切除术和Devine结肠造口术。他在术后36小时死亡。起始点是一个炎性息肉。
成人结肠-结肠套叠是一种罕见疾病,可能不会表现出儿童套叠的典型特征,从而造成诊断困境。高度的怀疑指数加上影像学检查将有助于快速准确的诊断。