Histopathologic findings in the lymphoid and reticuloendothelial system in pediatric HIV infection: a postmortem study.

G Quijano, M Siminovich, R Drut
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Abstract

The present report describes the histopathological features of lymphoreticular tissues in 29 pediatric autopsies of human immunodeficiency virus (HIV)-infected patients. Mean age for the whole group was 1.77 years; 68.9% and 62% of the cases were 2 years old or less and 1 year old or less at the time of death, respectively. Twenty-one cases were categorized as acquired immunodeficiency syndrome (AIDS) and the rest included seven HIV-positive newborns and infants and two infants belonging to a high-risk group. The thymus (24 cases) showed severe lymphoid depletion (atrophy) in 16 (66.6%) cases, microcystic transformation of Hassall's corpuscles (HCs) in 4, calcified HCs in 3, absence of HCs in 3, and plasmacytic infiltrates and Warthin-Finkeldey-type multinucleated giant cells (also found in lymph nodes and bowel lymphoid aggregates in the same case) in 1. Lymph nodes (25 cases) revealed extensive lymphocyte depletion (68%); selective follicular (2 cases) or paracortical (3 cases) atrophy; hemophagocytosis (44%); some type of hyperplasia (plasmacytosis, enlarged follicles) in 5 cases; some type of lymphadenitis (12 cases), 5 cases of which were due to opportunistic infections (cytomegalovirus, 2; histoplasmosis, cryptococcosis, Mycobacterium avium-intracellulare, 1 each). Main findings in the spleen (28 cases) were extensive lymphocyte depletion (10 cases), limited to the white pulp in 4 and including the red pulp in 7; some type of lymphoid hyperplasia (limited to white pulp in 6 cases and involving the red pulp in 5); hemophagocytosis (7 cases); and foci exhibiting a peculiar arrangement of spindle-shaped cells combined with capillaries, plasma cells, and occasionally siderophages in 11. These we have termed kaposiform areas due to the resemblance to the so-called inflammatory variant of Kaposi's sarcoma. This pattern was also recognized in lymph nodes of two cases. Although atrophy was the main theme, cases with hyperplasia were also noticed. The possible relationship, if it exists at all, between kaposiform areas and Kaposi's sarcoma remains to be established. No tumor was found in this series. No specific histopathologic pattern of lymphoid tissues atributable to HIV emerged form this study aside from kaposiform areas, a microscopic feature not previously reported in this circumstance in pediatrics.

儿童HIV感染的淋巴和网状内皮系统的组织病理学发现:一项死后研究。
本报告描述了29例人类免疫缺陷病毒(HIV)感染儿童尸体解剖的淋巴网状组织的组织病理学特征。整个组的平均年龄为1.77岁;68.9%和62%的病例死亡时年龄分别为2岁及以下和1岁及以下。21例被归类为获得性免疫缺陷综合征(艾滋病),其余包括7名艾滋病毒阳性的新生儿和婴儿以及2名属于高危群体的婴儿。胸腺(24例)出现严重淋巴细胞萎缩16例(66.6%),Hassall小体(HCs)微囊化4例,钙化3例,无HCs 3例,浆细胞浸润和warthin - finkeldey型多核巨细胞(也见于淋巴结和肠淋巴样聚集物)1例。淋巴结(25例)广泛淋巴细胞耗竭(68%);选择性滤泡萎缩(2例)或皮质旁萎缩(3例);hemophagocytosis (44%);不同类型增生(浆细胞增多、卵泡增大)5例;某些类型淋巴结炎(12例),其中5例为机会性感染(巨细胞病毒2例;组织胞浆菌病、隐球菌病、鸟胞内分枝杆菌各1例)。脾脏(28例)主要表现为广泛淋巴细胞耗竭(10例),局限于白髓4例,含红髓7例;某些类型的淋巴样增生(6例局限于白髓,5例累及红髓);噬血细胞症(7例);病灶表现出纺锤状细胞的特殊排列,与毛细血管、浆细胞和偶尔的侧噬细胞结合在一起。我们将这些区域称为卡波西样区,因为它们与卡波西肉瘤的炎症变体相似。在两例淋巴结中也发现了这种模式。虽然萎缩是主要的,但也注意到增生的病例。卡波西样区和卡波西肉瘤之间的可能关系,如果存在的话,还有待确定。本组未见肿瘤。在本研究中,除了卡样区外,没有出现可归因于HIV的淋巴组织的特定组织病理学模式,卡样区是以前在儿科中未报道过的一种显微镜特征。
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