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酷似布加综合征的肝脏上皮样血管内皮瘤

Epithelioid hemangioendothelioma of the liver mimicking Budd-Chiari syndrome.

作者信息

Walsh M M, Hytiroglou P, Thung S N, Fiel M I, Siegel D, Emre S, Ishak K G

机构信息

The Lillian and Henry M. Stratton-Hans Popper Department of Pathology, The Mount Sinai School of Medicine, City University of New York 10029, USA.

出版信息

Arch Pathol Lab Med. 1998 Sep;122(9):846-8.

PMID:9740148
Abstract

A case of epithelioid hemangioendothelioma of the liver in a 34-year-old man with clinical and radiologic findings suggestive of Budd-Chiari syndrome is reported. Despite clinical and radiologic findings, percutaneous liver biopsy was suspicious for epithelioid hemangioendothelioma. The patient underwent liver transplantation 2 months later, and histologic examination confirmed this diagnosis. Unusual histopathologic features included extensive areas of capillary-thin vascular structures with open lumina, lack of significant cytologic atypia in the majority of neoplastic cells, and areas with Budd-Chiari-like features in the hepatic parenchyma surrounding the tumor. The neoplastic cells were focally immunopositive for endothelial markers, such as factor VIII-related antigen and CD34 antigen. The unusual clinical presentation may have been due to tumor invasion and fibrous obliteration of terminal hepatic venules and sublobular veins. Epithelioid hemangioendothelioma should be considered when evaluating patients with clinical features of Budd-Chiari syndrome or veno-occlusive disease.

摘要

报告了一例34岁男性肝脏上皮样血管内皮瘤病例,其临床和影像学表现提示布加综合征。尽管有临床和影像学表现,但经皮肝活检仍怀疑为上皮样血管内皮瘤。患者2个月后接受了肝移植,组织学检查证实了这一诊断。不寻常的组织病理学特征包括广泛的毛细血管样薄血管结构区域,管腔开放,大多数肿瘤细胞缺乏明显的细胞异型性,以及肿瘤周围肝实质内出现布加综合征样特征的区域。肿瘤细胞对内皮标志物如因子VIII相关抗原和CD34抗原呈局灶性免疫阳性。这种不寻常的临床表现可能是由于肿瘤侵犯和终末肝小静脉及小叶下静脉的纤维性闭塞所致。在评估具有布加综合征或静脉闭塞性疾病临床特征的患者时,应考虑上皮样血管内皮瘤。

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