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具有胆管腺瘤样纤维瘤特征的未分类多房性胆内肿瘤病例。

A case of unclassified multicystic biliary tumor with biliary adenofibroma features.

机构信息

Department of Pathology & Microbiology, Saga University Faculty of Medicine, Saga, Japan.

出版信息

Pathol Int. 2012 Jul;62(7):506-10. doi: 10.1111/j.1440-1827.2012.02830.x. Epub 2012 May 10.

Abstract

A 40-year-old Japanese man was admitted to our hospital for evaluation of upper abdominal pain. Abdominal computed tomography (CT) revealed a well-circumscribed multicystic mass measuring approximately 7 × 6 cm. The mass contained a solid lesion measuring 3 × 2 cm. Biopsy of a swollen cervical lymph node led to a diagnosis of diffuse large B-cell lymphoma. After initial chemotherapy for lymphoma, the multicystic mass was surgically resected. The tumor was composed of a multicystic lesion and a solid lesion. Histopathologic examination of the multicystic lesion revealed that the locules were lined by biliary epithelium, demonstrating various degrees of cytological atypia. The stroma was fibrous, and the tumor showed marked apocrine snouts. Part of the tumor showed papillary growth with strong cytological atypia. The solid lesion showed tubulocystic proliferation of tumor cells, with prominent apocrine snouts, embedded in dense and partially hyalinized fibrous stroma. The morphology of the solid part was quite similar to that of reported biliary adenofibroma. Despite lengthy discussion, an appropriate pathological diagnosis could not be found among the current classifications of biliary tumor. The tumor was finally diagnosed as unclassified multicystic biliary tumor with adenofibroma features.

摘要

一位 40 岁的日本男性因上腹疼痛到我院就诊。腹部 CT 显示一个边界清楚的多囊性肿块,大小约为 7×6cm。肿块内有一个 3×2cm 的实性病灶。肿大的颈部淋巴结活检提示弥漫性大 B 细胞淋巴瘤。淋巴瘤初始化疗后,行多囊性肿块切除术。肿瘤由多囊性病变和实性病变组成。多囊性病变的组织病理学检查显示,腔隙由胆管上皮细胞衬里,表现出不同程度的细胞学异型性。基质为纤维性,肿瘤显示明显的大汗腺突起。部分肿瘤呈乳头状生长,有强烈的细胞学异型性。实性病变显示肿瘤细胞的小管囊状增生,伴有明显的大汗腺突起,嵌入致密和部分玻璃样化的纤维基质中。实性部分的形态与报道的胆管腺纤维瘤非常相似。尽管进行了长时间的讨论,但在当前的胆管肿瘤分类中仍无法找到合适的病理诊断。该肿瘤最终诊断为具有腺纤维瘤特征的未分类多囊性胆管肿瘤。

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