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胆囊原发性神经内分泌癌伴胰胆管合流异常 1 例

A case of primary neuroendocrine carcinoma of the gallbladder associated with anomalous union of the pancreaticobiliary duct.

机构信息

Department of Internal Medicine, Chonnam National University Hospital, Gwangju, Korea.

出版信息

Gut Liver. 2009 Sep;3(3):231-4. doi: 10.5009/gnl.2009.3.3.231. Epub 2009 Sep 30.

Abstract

Primary neuroendocrine carcinoma of the gallbladder is extremely rare because normal gallbladder mucosa does not contain neuroendocrine cells. Neuroendocrine cells can be detected at sites of intestinal metaplasia induced by chronic inflammation, which may be the initial step in the development of neuroendocrine tumor of the gallbladder. Anomalous union of the pancreaticobiliary duct (AUPBD) is an uncommon congenital anomaly that is frequently associated with choledocholithiasis, cholangitis, pancreatitis, and cancer of the gallbladder or bile duct. In AUPBD, cancers of the gallbladder and bile duct can be induced by chronic inflammation. We report herein a case of large-cell neuroendocrine tumor of the gallbladder associated with AUPBD.

摘要

原发性胆囊神经内分泌癌极为罕见,因为正常的胆囊黏膜不含神经内分泌细胞。在慢性炎症引起的肠上皮化生部位可检测到神经内分泌细胞,这可能是胆囊神经内分泌肿瘤发生的初始步骤。胰胆管合流异常(AUPBD)是一种罕见的先天性异常,常与胆总管结石、胆管炎、胰腺炎以及胆囊或胆管癌相关。在 AUPBD 中,慢性炎症可诱发胆囊和胆管癌。我们在此报告一例伴有 AUPBD 的胆囊大细胞神经内分泌癌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb53/2852714/3d1e78cf6c3f/gnl-3-231-g001.jpg

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