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胆囊完全性胰腺异位伴肥厚导管,形似腺肌瘤。

Complete pancreatic heterotopia of gallbladder with hypertrophic duct simulating an adenomyoma.

作者信息

Pilloni Luca, Cois Alessandro, Uccheddu Alessandro, Ambu Rossano, Coni Pierpaolo, Faa Gavino

机构信息

Istituto di Anatomia Patologica, Dipartimento di Citomorfologia, Universitá degli Studi di Cagliari, Via Ospedale 46, Cagliari 09124, Italy.

出版信息

World J Gastroenterol. 2006 Mar 21;12(11):1786-7. doi: 10.3748/wjg.v12.i11.1786.

Abstract

The gallbladder is an unusual location of pancreatic heterotopia, defined as the presence of pancreatic tissue lacking anatomical and vascular continuity with the main body of the gland. A 28-year-old man presented with anorexia, nausea and pain in the right upper abdomen. On physical examination, the abdomen was tender to palpation and Murphy sign was positive. The patient underwent a cholecystecomy. This case, in our opinion, is very interesting since it permits to consider a controversial issue in the pathology of the gallbladder. The histological appearance of ductal structure in pancreatic heterotopia resembles the histological picture of both Aschoff-Rokitansky (AR) sinuses and adenomyomas. This finding suggests that these lesions are linked by a common histogenetic origin. We suggest that the finding of an adenomyoma in the gallbladder should prompt an extensive sampling of the organ in order to verify the coexistence of pancreatic rests.

摘要

胆囊是胰腺异位的一个不寻常部位,胰腺异位定义为存在与胰腺主体缺乏解剖学和血管连续性的胰腺组织。一名28岁男性出现厌食、恶心和右上腹疼痛。体格检查时,腹部触诊有压痛,墨菲氏征阳性。该患者接受了胆囊切除术。我们认为这个病例非常有趣,因为它有助于思考胆囊病理学中一个有争议的问题。胰腺异位中导管结构的组织学表现类似于阿绍夫-罗基坦斯基(AR)窦和腺肌瘤的组织学图像。这一发现表明这些病变有共同的组织发生起源。我们建议,在胆囊中发现腺肌瘤应促使对该器官进行广泛取材,以证实胰腺残余组织的共存情况。

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