PJS并发肠套叠一例

One Case of the PJ Syndrome Complicated with Intussusception

摘要: PJS是一种少见的家族遗传性疾病，临床表现胃肠道息肉和皮肤黏膜黑色素沉着斑点。早期切除肠息肉可延长PJS患者的生存时间，对PJS家族成员进行致病基因检测有助于及早确诊以及预测癌变风险。 PJS is a rare hereditary disease, and clinical features were pigmented spots on the lips and oral mucosa with gastrointestinal tract polyposis. Early resection of the bowel polyps in PJS patients will prolong survival time, detect causative gene of PJS family members contribute to early diagnosis and early prediction of cancer risk.