Fatine Amine, Bouali Mounir, El Bakouri Abdelilah, ElHattabi Khalid, Bensardi Fatimazahra, Fadil Abdelaziz
Visceral Surgery Emergency Department, University Hospital Center Ibn Rochd, Casablanca, Morocco.
Faculty of Medecine and Pharmacy, Hassan II University, Casablanca, Morocco.
Ann Med Surg (Lond). 2021 May 12;66:102390. doi: 10.1016/j.amsu.2021.102390. eCollection 2021 Jun.
Retroperitoneal Retrocecal hernias are a rare variety of internal hernias and represent an unusual cause of bowel obstruction. Early diagnosis is based on CT scan and requires knowledge of the pathology in order to avoid small bowel resection. We report a case of retrocecal hernia treated surgically and review the characteristics and treatment of retrocecal hernias in the literature.
Our work is a retrospective case report with a descriptive aim concerning a patient operated for retrocecal hernia within the department of general surgery of CHU Ibn Rochd Casablanca.
A 72-year-old man presented to the emergency department with abdominal pain and vomiting that have been evolving for 9 days complicated by an occlusive syndrome 36 hours before the admission. The patient was apyretic, and the abdominal examination noted abdominal meteorism predominantly in the right iliac fossa, absence of abdominal scarring, and free hernial orifices. The abdominal X-ray showed air-fluid levels and the abdominopelvic CT scan found clumping of the dilated small intestines posteriorly and below the cecum. The diagnosis of retrocecal hernia was suspected and the patient was taken to the operating room. The operation was performed by laparotomy through a midline incision. On exploration, the cecum and ascending colon were pushed forward and viable bowel loops were incarcerated in a fossa located posteriorly and below the cecum. The procedure consisted of a collapse of the retrocecal ligaments by right coloparietal collapse.
A bowel obstruction in an apyretic patient without abdominal scarring or parietal hernia should suggest the diagnosis of internal hernia, which must be investigated.
腹膜后盲肠后疝是一种罕见的内疝类型,是肠梗阻的不常见原因。早期诊断基于CT扫描,需要了解其病理特征以避免小肠切除。我们报告一例经手术治疗的盲肠后疝病例,并复习文献中盲肠后疝的特征及治疗方法。
我们的研究是一项回顾性病例报告,旨在描述一名在卡萨布兰卡伊本·罗什德大学医院普通外科接受盲肠后疝手术的患者。
一名72岁男性因腹痛和呕吐9天就诊于急诊科,入院前36小时并发肠梗阻综合征。患者无发热,腹部检查发现主要在右下腹有肠胀气,无腹部瘢痕,无游离疝孔。腹部X线显示气液平面,腹部盆腔CT扫描发现扩张的小肠在盲肠后方及下方聚集。怀疑为盲肠后疝,遂将患者送入手术室。手术通过中线切口剖腹进行。术中探查发现,盲肠和升结肠向前推移,存活的肠袢嵌顿于盲肠后方及下方的一个隐窝内。手术过程包括通过右结肠旁沟塌陷使盲肠后韧带塌陷。
无发热、无腹部瘢痕或腹外疝的患者出现肠梗阻应提示内疝的诊断,必须进行进一步检查。