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获得性免疫缺陷综合征(AIDS)或艾滋病相关综合征(ARC)患者的淋巴结改变。45例病例的组织学、免疫组织病理学及超微结构研究。

Lymph node modification in patients with the acquired immunodeficiency syndrome (AIDS) or with AIDS related complex (ARC). A histological, immuno-histopathological and ultrastructural study of 45 cases.

作者信息

Diebold J, Marche C, Audouin J, Aubert J P, Le Tourneau A, Bouton C, Reynes M, Wizniak J, Capron F, Tricottet V

出版信息

Pathol Res Pract. 1985 Dec;180(6):590-611. doi: 10.1016/S0344-0338(85)80037-6.

Abstract

The authors present the results of a histopathological study on the lymph-nodes taken from 45 subjects suffering from either an AIDS or from a chronic adenopathy corresponding to the definition of AIDS related complex (ARC). The various aspects observed were classed as type I to type IV. The lymph-node modifications observed in the 29 patients with an ARC could be divided into three principle groups: an extensive follicular hyperplasia associated with other elementary lesions or type IA (25 lymph-nodes from 23 patients); changes resembling a multicentric Castleman syndrome or type IB (1 case); angioimmunoblastic-like (AIL) lesions or type II (2 cases) and an association of lesions of type II (7 lymph-nodes from 6 patients). During AIDS, the adenopathy usually disappears, and the small lymph-nodes removed, especially on autopsy, show an extensive lymphoid depletion (type III) with systematic sclerosis (15 lymph-nodes from 14 patients). When adenopathy persists, it is due to infections complications (tuberculosis, cryptococcosis, avian mycobacteriosis and Whipple's disease like lesions). Of the 10 patients in whom a Kaposi's sarcoma was observed, only 6 showed lymph-node involvement, or type IV. The different histopathological lesions seem to appear according to an evolving succession, proven by certain association of lesions and by successive biopsies. In our series, 17% of subjects with an ARC evolved to AIDS. Lymph-node biopsy allows a possible ARC to be implicated on the association of the following simple lesions: follicular hyperplasia with partial or total destruction of the perifollicular lymphocytic cisterna, infiltration of the germinative centres by streams of small lymphocytes, evolving to an aspect of a "burst" germinative centre and various sinusal reactions with, in particular, the presence of neutrophilic polynuclear cells. The biopsy also allows the forms with bad prognosis to be recognized: those with AIL-like aspect or multicentric Castleman-like syndrome, which seems to represent a particular evolutive form. Finally, it also detects, in certain cases, the localization of a Kaposi syndrome, signalling the passage to AIDS. The immunopathological studies present a double interest. Firstly, they offer arguments in favour of the diagnosis: increase in the number of T8 lymphocytes in the germinative centres with the formation of small clusters and disruption of the network of dendritic reticular cells, and the inversion of the T4/T8 ratio in the extra-follicular cortical regions, by either a decrease in T4 lymphocytes or by an increase in T8 lymphocytes.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

作者展示了一项组织病理学研究的结果,该研究针对取自45名患者的淋巴结,这些患者要么患有艾滋病,要么患有符合艾滋病相关综合征(ARC)定义的慢性腺病。观察到的各种情况被分为I型至IV型。在29例ARC患者中观察到的淋巴结改变可分为三个主要组:与其他基本病变相关的广泛滤泡增生或IA型(来自23例患者的25个淋巴结);类似多中心Castleman综合征的改变或IB型(1例);血管免疫母细胞样(AIL)病变或II型(2例)以及II型病变的组合(来自6例患者的7个淋巴结)。在艾滋病期间,腺病通常会消失,切除的小淋巴结,尤其是尸检时的淋巴结,显示出广泛的淋巴细胞耗竭(III型)并伴有系统性硬化(来自14例患者的15个淋巴结)。当腺病持续存在时,是由于感染并发症(结核病、隐球菌病、鸟型分枝杆菌病和类惠普尔病样病变)。在观察到卡波西肉瘤的10例患者中,只有6例显示有淋巴结受累,即IV型。不同的组织病理学病变似乎按照一种演变顺序出现,这由病变的某些关联以及连续活检所证实。在我们的系列研究中,17%的ARC患者发展为艾滋病。淋巴结活检通过以下简单病变的关联可提示可能患有ARC:滤泡增生伴有滤泡周围淋巴细胞池部分或完全破坏、生发中心被小淋巴细胞流浸润、演变为“爆发”样生发中心以及各种窦状反应,特别是存在嗜中性多形核细胞。活检还能识别预后不良的类型:具有AIL样外观或多中心Castleman样综合征的类型,这似乎代表一种特殊的演变形式。最后,在某些情况下,它还能检测到卡波西综合征的定位,标志着已发展为艾滋病。免疫病理学研究具有双重意义。首先,它们为诊断提供依据:生发中心T8淋巴细胞数量增加,形成小簇,树突状网状细胞网络破坏,以及滤泡外皮质区域T4/T8比值倒置,表现为T4淋巴细胞减少或T8淋巴细胞增加。(摘要截断于400字)

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