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伴有浸润性癌的胆管腺纤维瘤:病例报告及文献复习

Biliary Adenofibroma with Invasive Carcinoma: Case Report and Review of the Literature.

作者信息

Godambe Anjali, Brunt Elizabeth M, Fulling Keith H, Reza Kermanshahi Taher

机构信息

Ameripath Indiana, Indianapolis, IN, USA.

Department of Pathology and Immunology, Washington University, St. Louis, MO, USA.

出版信息

Case Rep Pathol. 2016;2016:8068513. doi: 10.1155/2016/8068513. Epub 2016 Jan 13.

Abstract

We report a case of biliary adenofibroma with an invasive carcinoma in a 71-year-old female who presented with bilateral upper abdominal pain. Imaging revealed a 6.3 cm heterogeneously enhancing mass in the left lateral segment of the liver. Histologically, the adenofibroma showed the characteristic components as previously described of biliary adenofibromata, namely, cystic and tubular structures lined by cuboidal to low columnar biliary type epithelium and a dense fibrous stroma composed of spindled cells. Intimately admixed with the adenofibroma was a distinct tumor composed of malignant clear cells which demonstrated stromal and vascular invasion. Although mitotic figures were inconspicuous, Ki67 was brisk and p53 demonstrated 25-50% positivity. Sections also showed a von Meyenberg complex located adjacent to the tumor. This case expands the understanding of this rare tumor and proves two important assertions from previous case reports. First, the presence of an associated von Meyenberg complex with similar morphology and immunohistochemical staining pattern suggests that biliary adenofibromata and von Meyenberg complexes may share related histogenesis. Second, biliary adenofibromata harbor malignant potential and may show malignant transformation. Furthermore, this case highlights the need for these rare tumors to be followed aggressively, as their biological behavior is poorly understood.

摘要

我们报告一例71岁女性的胆管腺纤维瘤合并浸润性癌,该患者表现为双侧上腹部疼痛。影像学检查显示肝脏左外叶有一个6.3厘米的不均匀强化肿块。组织学上,腺纤维瘤显示出如先前所述的胆管腺纤维瘤的特征性成分,即由立方形至低柱状胆管型上皮衬里的囊性和管状结构以及由梭形细胞组成的致密纤维性间质。与腺纤维瘤紧密混合的是一个由恶性透明细胞组成的独特肿瘤,该肿瘤表现出间质和血管浸润。尽管有丝分裂象不明显,但Ki67增殖活跃,p53阳性率为25%-50%。切片还显示在肿瘤附近有一个梅氏复合体。该病例扩展了对这种罕见肿瘤的认识,并证实了先前病例报告中的两个重要论断。首先,存在形态学和免疫组化染色模式相似的相关梅氏复合体,提示胆管腺纤维瘤和梅氏复合体可能具有相关的组织发生。其次,胆管腺纤维瘤具有恶性潜能,可能发生恶性转化。此外,该病例强调了对这些罕见肿瘤进行积极随访的必要性,因为它们的生物学行为尚不清楚。

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