Turner R R, Meyer P R, Taylor C R, Gill P S, Hofman F M, Nichols P, Rasheed S, Levine A M
Am J Clin Pathol. 1987 Jul;88(1):10-9. doi: 10.1093/ajcp/88.1.10.
Immunohistologic analysis of cellular changes in serial lymph node biopsies of eight patients with persistent generalized lymphadenopathy (PGL) syndrome was performed and correlated with clinical and laboratory findings to better determine the natural history of human immunodeficiency virus (HIV) infection. The authors observed decreased follicle size and area in the second biopsies of six of the eight patients, associated in some with increased numbers of B-cells in medullary regions (four of eight) and more involuted follicles (four of eight). Five cases showed progressively increased paracortical areas in the second biopsies, with increased numbers of T-cytotoxic/suppressor cells and decreased T-helper cells. Seven of the patients also had a progressive loss of T-helper cells in the peripheral blood. These findings provide tissue and peripheral blood evidence for progressive immunologic deterioration in some patients with PGL.
对八例持续性全身性淋巴结病(PGL)综合征患者的系列淋巴结活检进行细胞变化的免疫组织学分析,并将其与临床和实验室检查结果相关联,以更好地确定人类免疫缺陷病毒(HIV)感染的自然病程。作者观察到,八名患者中有六名在第二次活检时卵泡大小和面积减小,其中一些患者伴有髓质区域B细胞数量增加(八名中的四名)和更多萎缩卵泡(八名中的四名)。五例患者在第二次活检时副皮质区逐渐增大,T细胞毒性/抑制细胞数量增加,T辅助细胞减少。七名患者外周血中的T辅助细胞也逐渐减少。这些发现为一些PGL患者的免疫功能进行性恶化提供了组织和外周血证据。