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再探风湿性阿绍夫小体:细胞成分的免疫组织学重新评估

Rheumatic Aschoff nodules revisited: an immunohistological reappraisal of the cellular component.

作者信息

Fraser W J, Haffejee Z, Cooper K

机构信息

Department of Anatomical Pathology, School of Pathology, South African Institute for Medical Research, Johannesburg, South Africa.

出版信息

Histopathology. 1995 Nov;27(5):457-61. doi: 10.1111/j.1365-2559.1995.tb00310.x.

DOI:10.1111/j.1365-2559.1995.tb00310.x
PMID:8575737
Abstract

Rheumatic fever is still the leading cause of acquired heart disease in children and young adults in developing countries. Recent reports have documented a rising incidence of rheumatic fever in both the USA and Europe. The disease is characterized by specific lesions in the heart muscle and valves called Aschoff nodules. The Aschoff nodule has been neglected in the last few decades as most of the studies were conducted in the 1960s on autopsy tissues. This study examines Aschoff nodules using heart valve material obtained at valve surgery with updated commercially available immunohistochemical antibodies to determine the phenotypic characteristics of the cells involved in the formation of these lesions. Fifteen cases of rheumatic valvulitis, as indicated by the presence of Aschoff nodules, were examined. The Anitschkow and Aschoff cells stained prominently with macrophage markers. Three stages of nodules with Aschoff and Anitschkow cells were identified: stage 1, central fibrinoid necrosis without lymphocytes, stage 2 with occasional T lymphocytes (< 10) and stage 3 with lymphoid aggregates containing both T- and B-lymphocytes (with occasional admixed macrophages). We propose that the stage 1 lesion is the earliest granulomatous stage with the lymphoid aggregates being a later stage in the development of Aschoff nodules. The Aschoff and Anitschkow cells demonstrated mitotic activity and stained with antibodies to the proliferation cell nuclear antigen (PCNA) suggesting that the multinucleated giant cells may be formed, at least partially, by nuclear division rather than fusion.

摘要

在发展中国家,风湿热仍是儿童和青年获得性心脏病的主要病因。最近的报告显示,美国和欧洲的风湿热发病率都在上升。该疾病的特征是心肌和瓣膜出现特定病变,称为阿绍夫小体。在过去几十年里,阿绍夫小体一直被忽视,因为大多数研究是在20世纪60年代对尸检组织进行的。本研究使用瓣膜手术中获取的心脏瓣膜材料,并结合最新的市售免疫组化抗体来检测阿绍夫小体,以确定参与这些病变形成的细胞的表型特征。对15例存在阿绍夫小体的风湿性瓣膜炎病例进行了检查。阿绍夫细胞和安itschkow细胞与巨噬细胞标志物染色明显。确定了含有阿绍夫细胞和安itschkow细胞的小体的三个阶段:第1阶段,中央纤维蛋白样坏死,无淋巴细胞;第2阶段,偶尔有T淋巴细胞(<10个);第3阶段,有含有T淋巴细胞和B淋巴细胞的淋巴样聚集物(偶尔有混合巨噬细胞)。我们认为,第1阶段病变是最早的肉芽肿阶段,淋巴样聚集物是阿绍夫小体发展的后期阶段。阿绍夫细胞和安itschkow细胞表现出有丝分裂活性,并用增殖细胞核抗原(PCNA)抗体染色,提示多核巨细胞可能至少部分是由核分裂而非融合形成的。

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