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十二指肠壁肌上皮错构瘤

Myoepithelial hamartoma of the duodenal wall.

作者信息

Ryan A, Lafnitzegger J R, Lin D H, Jakate S, Staren E D

机构信息

Rush-Presbyterian-St. Luke's Medical Center, Department of Pathology, Chicago, IL 60612, USA.

出版信息

Virchows Arch. 1998 Feb;432(2):191-4. doi: 10.1007/s004280050155.

Abstract

A rare case of myoepithelial hamartoma of the duodenal wall is presented, and previous case reports found in the literature are reviewed. Myoepithelial hamartomas are thought to arise from displaced pancreatic anlage present along the gastrointestinal tract during embryogenesis, which can differentiate into various pancreatic elements; the most highly differentiated form is heterotopic pancreas. An alternative theory is pancreatic metaplasia of endodermal tissues. We describe a 41-year-old man who presented with abdominal pain and vomiting. CT scanning revealed a mass at the head of the pancreas. A pancreaticoduodenectomy was performed for presumed cystadenoma. Histology of the mass revealed a disorderly arrangement of smooth muscle, dilated and nondilated ducts, pancreatic acinar tissue and mucus glands. The relationship of myoepithelial hamartomas involving the small bowel to similar lesions in the stomach, bile ducts and gallbladder is discussed.

摘要

本文报告一例罕见的十二指肠壁肌上皮错构瘤,并复习了文献中既往的病例报告。肌上皮错构瘤被认为起源于胚胎发育过程中沿胃肠道移位的胰腺原基,其可分化为各种胰腺成分;分化程度最高的形式是异位胰腺。另一种理论是内胚层组织的胰腺化生。我们描述了一名41岁男性,其表现为腹痛和呕吐。CT扫描显示胰腺头部有一肿块。因疑似囊腺瘤而行胰十二指肠切除术。肿块的组织学检查显示平滑肌、扩张和未扩张的导管、胰腺腺泡组织和黏液腺排列紊乱。文中还讨论了累及小肠的肌上皮错构瘤与胃、胆管和胆囊中类似病变的关系。

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