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[血管免疫母细胞性淋巴结病]

[Angioimmunoblastic lymphadenopathy].

作者信息

Bak M, Garam T, Bakács T, Döbrentey E, Bodó M, Petrányi G

出版信息

Morphol Igazsagugyi Orv Sz. 1981 Jan;21(1):26-33.

PMID:6973692
Abstract

Cytological, histological and ultrastructural characteristics of a cose of an extranodal and nodal angioimmunoblastic lymphadenopathy persisting during several years are given. Angiomatous proliferation in the case reported seemed to be identical both in the lymph node and in the cutaneous infiltration. Types of cells seen in the angioimmunablastic lymphadenopathy did not differ from those of other immunoreactive processes. In the extranodal infiltrates in addition to other phenomena thickening of the immunological techniques decrease of the natural cytotoxicity and the number of T-lymphocytes could be observed.

摘要

给出了一例结外和结内血管免疫母细胞性淋巴结病持续数年的细胞学、组织学和超微结构特征。所报道病例中的血管瘤样增生在淋巴结和皮肤浸润中似乎是相同的。血管免疫母细胞性淋巴结病中所见的细胞类型与其他免疫反应性过程中的细胞类型并无差异。在结外浸润中,除其他现象外,还可观察到免疫技术增厚、自然细胞毒性降低以及T淋巴细胞数量减少。

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