SYSTEMIC HEMANGIOMATOSIS
SYSTEMIC HEMANGIOMATOSIS
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系统性血管瘤病
DOI：
10.1111/j.1440-1827.1986.tb00219.x
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发表时间：
1986
影响因子：
2.2
通讯作者：
W. Mori
中科院分区：
文献类型：
--
作者：
H. Sugimura;T. Tange;K. Yamaguchi;W. Mori
本文报告一例罕见血管形成肿瘤的尸检病例。这种肿瘤的分布局限于造血系统的器官，如脾、肝和全骨髓。尽管由于广泛播散，它可能被认为是某些脾血管肉瘤的变种，但其良性的组织学特征和特殊的分布表明它是错构瘤性质的。从系统性血管瘤病的角度简要回顾了文献中另外几个类似的病例。
An autopsy case of unusual vasoformative tumor is presented. The distribution of this tumor was restricted to the organ of the hematopoietic system such as the spleen, liver, and whole bone marrow. Although it may be considered as a variant of certain splenic hemangiosarcoma because of widespread dissemination, both the benign‐looking histological features and specific distribution of this tumor suggest its hamartomatous nature. Several additional similar cases in the literatures are briefly reviewed from the viewpoint of systemic hemangiomatosis.