Nakamura T, Watanabe M, Hotchi M, Fujimori N, Mizuno M
Department of Pathology, Shinshu University School of Medicine, Matsumoto, Japan.
Acta Pathol Jpn. 1987 Aug;37(8):1337-46. doi: 10.1111/j.1440-1827.1987.tb00466.x.
Two autopsy cases of neoplastic angioendotheliomatosis (NAE) were presented. Both patients were elderly woman, characterized by an ascending progression of transverse myelopathy and abnormal brain shadows similar to metastatic tumor in computer tomographic examination in Case 1, and by typical clinical features of cerebral infarction in Case 2. Postmortem examinations of both cases revealed an exclusive intravascular distribution of large atypical cells in generalized organs, especially in the central nervous system, and associated multiple cerebral infarcts and, in Case 1, widespread demyelination of the spinal cord. There were no distinct lesions suggestive of a primary focus. In both cases only a few atypical cells were immunohistochemically positive for factor VIII-related antigen, likely due to non-specific absorption of serum factor VIII into the cells. On the other hand, almost all of the atypical cells were immunoreactive for LN-1, LN-2, and leukocyte common antigen, suggestive of lymphocytic (B cell) origin.
本文报告了两例肿瘤性血管内皮瘤病(NAE)的尸检病例。两名患者均为老年女性,病例1的特征是进行性上升性横贯性脊髓病,计算机断层扫描显示脑部阴影异常,类似转移性肿瘤;病例2具有典型的脑梗死临床特征。两例尸检均显示,全身器官,尤其是中枢神经系统中,大的非典型细胞仅在血管内分布,并伴有多发性脑梗死,病例1还伴有脊髓广泛脱髓鞘。未发现提示原发灶的明显病变。在两例中,仅有少数非典型细胞对VIII因子相关抗原呈免疫组化阳性,这可能是由于血清VIII因子非特异性吸收进入细胞所致。另一方面,几乎所有非典型细胞对LN-1、LN-2和白细胞共同抗原呈免疫反应,提示其起源于淋巴细胞(B细胞)。