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血管免疫母细胞性淋巴结病的免疫病理学

Immunopathology of angioimmunoblastic lymphadenopathy.

作者信息

Jones D B, Castleden M, Smith J L, Mepham B L, Wright D H

出版信息

Br J Cancer. 1978 Jun;37(6):1053-62. doi: 10.1038/bjc.1978.153.

Abstract

Eight patients with angioimmunoblastic lymphadenopathy have been studied by a variety of immunological and pathological techniques. They exhibited a spectrum of immunological reactivities that, in this small series, could be roughly correlated with survival. Those patients with relative B-cell predominance as shown by cell marker studies, histologically showed large numbers of plasma cells, and this pattern was associated in 3 of our patients with a survival of 3 years or more. T-cell predominance or both B- and T-cell depletion was associated histologically with large numbers of blast cells and eosinophils, but with few plasma cells. These patients responded poorly to therapy and had short survival times. One patient with B-cell predominance subsequently died of a histiocytic lymphoma.

摘要

我们运用多种免疫和病理技术对8例血管免疫母细胞性淋巴结病患者进行了研究。他们呈现出一系列免疫反应性,在这个小样本系列中,这些反应性大致与生存率相关。细胞标志物研究显示相对B细胞占优势的患者,组织学上可见大量浆细胞,在我们的3例患者中,这种模式与3年或更长时间的生存期相关。T细胞占优势或B细胞和T细胞均减少在组织学上与大量母细胞和嗜酸性粒细胞相关,但浆细胞较少。这些患者对治疗反应不佳,生存期较短。1例B细胞占优势的患者随后死于组织细胞性淋巴瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a83/2009654/003e85e4b5e5/brjcancer00164-0185-a.jpg

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