Pallesen G, Gerstoft J, Mathiesen L
Scand J Immunol. 1987 Jan;25(1):83-91. doi: 10.1111/j.1365-3083.1987.tb01049.x.
Lymph nodes from 40 homosexuals with persistent, generalized lymphadenopathy were studied for histological and immunohistological changes and classified into histological stages based on the progressive destruction of lymph node follicles in association with progression of the disease. Three patterns were recognized: stage I was characterized by follicular hyperplasia, mantle zone depletion, and follicular fragmentation in the absence of vasculitis, stage II by signs of follicular involution, and stage III by depletion of follicles and dendritic reticulum cells with development of diffuse pattern. The T zone was gradually depleted of CD4-positive lymphocytes, but on further progression, lymphocytic depletion (which also involved the CD8-positive cells) and fibrosis prevailed. The 40 lymph nodes from homosexuals were classified as stage I in 18 cases, stage II in 11, and stage III in 10. One case did not fulfil our histological criteria for LAV/HTLV-III lymphadenitis, although this patient was seropositive. Convincing correlation was found between histological stages and clinical and laboratory data. The triad of follicular hyperplasia, mantle zone depletion, and follicular fragmentation, in the absence of vasculitis, appears pathognomonic for the early disease. The diffuse pattern, however, may be seen in different disease entities.
对40例患有持续性全身性淋巴结病的同性恋者的淋巴结进行了组织学和免疫组织学变化研究,并根据疾病进展过程中淋巴结滤泡的逐渐破坏情况将其分为组织学阶段。识别出三种模式:I期的特征是滤泡增生、套区缺失和滤泡破碎,无血管炎;II期有滤泡退化的迹象;III期是滤泡和树突状网状细胞缺失,出现弥漫性模式。T区的CD4阳性淋巴细胞逐渐减少,但进一步发展时,淋巴细胞减少(也涉及CD8阳性细胞)和纤维化占主导。40例同性恋者的淋巴结中,18例为I期,11例为II期,10例为III期。1例患者不符合我们关于淋巴结病相关病毒/人嗜T淋巴细胞病毒III型淋巴结炎的组织学标准,尽管该患者血清学呈阳性。在组织学阶段与临床和实验室数据之间发现了令人信服的相关性。在无血管炎的情况下,滤泡增生、套区缺失和滤泡破碎三联征似乎是早期疾病的特征性表现。然而,弥漫性模式可见于不同的疾病实体。