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两名肺透明变性肉芽肿患者的免疫异常

Immunologic abnormalities in two patients with pulmonary hyalinizing granuloma.

作者信息

Schlosnagle D C, Check I J, Sewell C W, Plummer A, York R M, Hunter R L

出版信息

Am J Clin Pathol. 1982 Aug;78(2):231-5. doi: 10.1093/ajcp/78.2.231.

Abstract

Pulmonary hyalinizing granuloma (PHG) is a disease of slowly enlarging pulmonary nodules made up of dense bundles of collagen accompanied by an infiltrate of chronic inflammatory cells. The etiology is unknown. Although it has been suggested that the lesions represent an exaggerated immune response to unidentified agents, results of a detailed immunologic work-up of these patients have not been published. This report presents the laboratory findings of two patients with biopsy-proven PHG who have been followed four and eighteen years. Autoantibodies were detected (antinuclear antibody, rheumatoid factor, and positive antiglobulin tests), although clinically there was no evidence of a specific collagen-vascular disorder. Both patients had elevated levels of circulating immune complexes. These data suggest that immune complex mechanisms may be important in the pathogenesis of PHG.

摘要

肺透明变性肉芽肿(PHG)是一种由致密的胶原束伴慢性炎症细胞浸润组成的、肺部结节逐渐增大的疾病。其病因不明。尽管有人提出这些病变代表对不明病原体的过度免疫反应,但这些患者详细的免疫检查结果尚未发表。本报告介绍了两名经活检证实为PHG且分别随访了4年和18年的患者的实验室检查结果。检测到自身抗体(抗核抗体、类风湿因子和阳性抗球蛋白试验),尽管临床上没有特定胶原血管疾病的证据。两名患者循环免疫复合物水平均升高。这些数据表明免疫复合物机制可能在PHG的发病机制中起重要作用。

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