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[恶性血管内皮瘤病作为脑血管供血不足的罕见病因]

[Malignant angioendotheliomatosis as a rare cause of cerebrovascular insufficiency].

作者信息

Dietzmann K, Franke D, Diete S, Schmitt J, von Bossányi P

机构信息

Institut für Pathologische Anatomie, Medizinischen Akademie Magdeburg.

出版信息

Acta Histochem Suppl. 1992;42:91-8.

PMID:1584992
Abstract

Malignant angioendotheliomatosis, so called intravascular malignant lymphomatosis or angiotropic lymphoma, was found in cerebral hemispheres, spinal cord and nerve roots of a 50-year-old woman who died 4 months after onset of neurological symptoms. The pathological findings were characterised by neoplastic cells within the lumina and wall of small vessels as well as by multiple infarcts in the CNS. Vascular occlusions were caused by tumor cells and secondary changes of the wall. Positive reactions of Common Leucocyte Antigen and B-cell-markers support the idea of a lymphoid origin for the tumor cells. The differentiation to the angiocentric lymphoma as a T-cell tumor and the obscure pathogenesis of this neoplastic process must be clarified in the future.

摘要

恶性血管内皮瘤病,即所谓的血管内恶性淋巴瘤或亲血管性淋巴瘤,在一名50岁女性的大脑半球、脊髓和神经根中被发现,该女性在出现神经症状4个月后死亡。病理结果的特征是小血管管腔和管壁内有肿瘤细胞以及中枢神经系统内有多处梗死。血管闭塞是由肿瘤细胞和血管壁的继发性改变引起的。共同白细胞抗原和B细胞标志物的阳性反应支持肿瘤细胞起源于淋巴组织的观点。未来必须阐明向作为T细胞肿瘤的血管中心性淋巴瘤的分化以及这种肿瘤过程的不明发病机制。

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