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肝淋巴管瘤病:两例报告及免疫组织化学研究

Hepatic lymphangiomatosis: report of two cases, with an immunohistochemical study.

作者信息

Haratake J, Koide O, Takeshita H

机构信息

Department of Pathology and Oncology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.

出版信息

Am J Gastroenterol. 1992 Jul;87(7):906-9.

PMID:1615949
Abstract

Two cases of hepatic lymphangiomatosis were examined. One tumor was noted incidentally at autopsy, and the other tumor was removed by operation. These liver tumors could not be detected by the naked eye, but ill-defined lace-like areas were seen. Microscopically, small cystic spaces were irregularly aggregated in the hepatic parenchyma and, in part, in the portal tracts. Faintly stained lymph-like material without any erythrocytes was found in the spaces. The silver impregnation method confirmed that most of the cystic lumina were dilated Disse's spaces. Also, some of them were directly connected with lymph vessels in the portal tracts. Thin lining cells along the internal surface of these cystic channels could not be positively stained by Ulex europaens 1 or factor 8-related antigen, both of which were present in the endothelium of the blood vessels in the portal tracts. We describe herein this rare lymphangiomatosis of the liver, with special reference to its immunohistochemistry.

摘要

对两例肝淋巴管瘤病进行了检查。其中一个肿瘤是在尸检时偶然发现的,另一个肿瘤通过手术切除。这些肝脏肿瘤肉眼无法检测到,但可见边界不清的花边状区域。显微镜下,小囊腔在肝实质内不规则聚集,部分位于门管区。囊腔内发现淡染的淋巴样物质,无任何红细胞。银浸染法证实大多数囊腔为扩张的狄氏间隙。此外,其中一些直接与门管区的淋巴管相连。这些囊性通道内表面的薄衬里细胞不能被荆豆凝集素1或因子Ⅷ相关抗原阳性染色,而这两种物质均存在于门管区血管内皮中。我们在此描述这种罕见的肝淋巴管瘤病,并特别提及了其免疫组织化学情况。

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