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首页> 外文期刊>Oncology, Gastroenterology and Hepatology Reports >Recurrent Intussusception Secondary to Multiple Peutz-jegher polyps: An Unusual Case with Review of Literature
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Recurrent Intussusception Secondary to Multiple Peutz-jegher polyps: An Unusual Case with Review of Literature

机译：继发性肠套叠继发于多个Peutz-jegher息肉：一个不寻常的病例，并有文献复习

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摘要

Peutz-Jegher polyps are hamartomas of the small bowel which occur as part of the Peutz- Jegher syndrome, a rare autosomal dominant condition characterized by gastrointestinal polyps and mucocutaneous melanotic pigmentation. Here we report the case of a young male suffering from this syndrome who presented with acute intestinal obstruction due to intussception. Exploratory laparotomy was done which revealed jejuno-jejunal and jejunoileal intussusceptions for which resection and anastomosis was done. There were multiple intraluminal polyps in the jejunum which on histopathological examination, showed features of Peutz-Jegher Polyp. Patient behaved well in the post-operative period and is still on follow up with us.
机译：Peutz-Jegher息肉是小肠错构瘤，是Peutz-Jegher综合征的一部分，这是一种罕见的常染色体显性疾病，以胃肠息肉和粘膜皮肤黑色素沉着为特征。在这里，我们报告一位患有这种综合征的年轻男性，由于肠套叠而出现急性肠梗阻的病例。进行了探索性剖腹手术，揭示了空肠-空肠和空肠油性肠套叠，并进行了切除和吻合。空肠中有多个管腔内息肉，经组织病理学检查显示有Peutz-Jegher息肉的特征。病人在术后期间表现良好，并且仍在跟进我们。

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