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风湿性心肌炎的阿绍夫小体是源于组织细胞的肉芽肿性病变。

Aschoff bodies of rheumatic carditis are granulomatous lesions of histiocytic origin.

作者信息

Love G L, Restrepo C

机构信息

Department of Pathology, Louisiana State University Medical Center, New Orleans.

出版信息

Mod Pathol. 1988 Jul;1(4):256-61.

PMID:3070554
Abstract

The histogenesis of the Aschoff body of rheumatic carditis is controversial. Proliferative Aschoff bodies in heart sections from 6 patients with acute rheumatic heart disease were tested by avidin-biotin peroxidase labeling methods for the presence of desmin, muscle-specific actin, S-100, neurofilament, leukocyte common antigen, receptor for Ulex europeus I lectin, Factor VIII-related antigen, vimentin, alpha 1-antichymotrypsin, and myeloid/histiocyte antigen. Lack of Aschoff body labeling for desmin and muscle-specific actin, S-100 and neurofilament, and Ulex europeus I and Factor VIII-related antigen is not consistent with histogenesis from smooth or striated cardiac muscle, nerve or nerve sheath, and lymphatic or vascular endothelium, respectively. Strong labeling of Aschoff body cells for vimentin is evidence for a mesenchymal origin, and labeling for myeloid/histiocyte antigen is consistent with a histiocytic origin. Furthermore, weak, variable labeling of Aschoff body cells for leukocyte common antigen suggests that at least some Aschoff body cells were originally derived from blood-borne monocytes. Both multinucleated Aschoff cells and "owl's eye," Anitschkow cells label identically, suggesting a common origin. Alpha 1-Antichymotrypsin, a widely utilized marker of histiocytes, was unexpectedly negative. Perhaps histiocytes that form Aschoff bodies do not express this lysosomal enzyme. Aschoff bodies appear to be a unique and distinctive form of granuloma.

摘要

风湿性心肌炎阿绍夫小体的组织发生存在争议。采用抗生物素蛋白-生物素过氧化物酶标记法,对6例急性风湿性心脏病患者心脏切片中的增殖性阿绍夫小体进行检测,以确定是否存在结蛋白、肌肉特异性肌动蛋白、S-100、神经丝、白细胞共同抗原、欧洲荆豆I凝集素受体、VIII因子相关抗原、波形蛋白、α1抗糜蛋白酶和髓样/组织细胞抗原。阿绍夫小体对结蛋白和肌肉特异性肌动蛋白、S-100和神经丝、欧洲荆豆I和VIII因子相关抗原均无标记,这分别与平滑肌或横纹肌、神经或神经鞘、淋巴管或血管内皮的组织发生不一致。阿绍夫小体细胞对波形蛋白有强标记,证明其起源于间充质,对髓样/组织细胞抗原的标记与组织细胞起源一致。此外,阿绍夫小体细胞对白细胞共同抗原的标记较弱且变化不定,提示至少部分阿绍夫小体细胞最初来源于血源性单核细胞。多核阿绍夫细胞和“枭眼”样阿尼奇科夫细胞的标记相同,提示它们有共同起源。α1抗糜蛋白酶是一种广泛应用的组织细胞标志物,结果却意外呈阴性。或许形成阿绍夫小体的组织细胞不表达这种溶酶体酶。阿绍夫小体似乎是一种独特且有别于其他的肉芽肿形式。

相似文献

1
Aschoff bodies of rheumatic carditis are granulomatous lesions of histiocytic origin.风湿性心肌炎的阿绍夫小体是源于组织细胞的肉芽肿性病变。
Mod Pathol. 1988 Jul;1(4):256-61.
2
Immunohistochemical and histochemical profile of Aschoff bodies in rheumatic carditis in excised left atrial appendages: an immunoperoxidase study in fresh and paraffin-embedded tissue.切除的左心耳中风湿性心肌炎阿绍夫小体的免疫组织化学和组织化学特征:新鲜组织和石蜡包埋组织的免疫过氧化物酶研究
Int J Cardiol. 1992 Feb;34(2):199-207. doi: 10.1016/0167-5273(92)90156-w.
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[Aschoff-Talalaev granuloma (problems of histogenesis, evolution and clinical significance)].[阿绍夫-塔拉莱夫肉芽肿(组织发生、演变及临床意义问题)]
Revmatologiia (Mosk). 1986 Jan-Mar(1):45-51.
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Degeneration of cardiac muscle followed by cell transformation, regeneration and fibrogenesis in rheumatic fever.风湿热时心肌变性,随后发生细胞转化、再生和纤维生成。
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[Pathology review. Acute rheumatic fever--Aschoff nodule].[病理学回顾。急性风湿热——阿绍夫小体]
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[Evaluating active rheumatism with biopsy of the ventricular myocardium].
Zhonghua Xin Xue Guan Bing Za Zhi. 1992 Oct;20(5):301-2, 325.
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Evidence that Aschoff bodies of rheumatic myocarditis develop from injured myofibers.风湿性心肌炎的阿绍夫小体由受损肌纤维发展而来的证据。
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Immunohistochemical characterisation of Aschoff nodules and endomyocardial inflammatory infiltrates in left atrial appendages from patients with chronic rheumatic heart disease.慢性风湿性心脏病患者左心耳中Aschoff小结和心肌内膜炎性浸润的免疫组织化学特征
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Anitschkow myocytes or cardiac histiocytes in human hearts.
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Histopathology. 1995 Nov;27(5):457-61. doi: 10.1111/j.1365-2559.1995.tb00310.x.

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