Richter’s femoral hernia with spontaneous enterocutaneous fistula: a case report
نویسندگان
چکیده
Richter’s hernia is rare and hard to diagnosis. We reported a male elder with Richter’s hernia in the right femoral tube. It was firstly treated as lymphnoditis, and finally presented as enterocutaneous fistula. We performed wedge excision and suture of the ileum wall defect under laparoscopy, local debridement of the groin and repair for the femoral ring. He had the good recovery with regular follow-up.
منابع مشابه
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BACKGROUND Richter's hernia is a high-risk ischaemic gastrointestinal disorder that is typically diagnosed in a delayed manner due to a lack of obvious symptoms. Spontaneous umbilical enterocutaneous fistula (ECF) resulting from an incarcerated Richter's hernia is extremely rare. CASE PRESENTATION A 62-year-old female presented with a chief complaint of recurrent umbilical region infection fo...
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A 70-year-old woman presented with a short history of a spontaneous enterocutaneos fistula in the left inguinal region. A laparotomy revealed a fistulizing Richter's hernia. The fistulizing small bowel segment was resected and the femoral hernia repaired from below. Although rare, a complicating Richter's hernia should be considered in the differential diagnosis of a groin fistula.
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تاریخ انتشار 2016