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肺透明变性肉芽肿:与多发性硬化症的一种不寻常关联。

Pulmonary hyalinizing granuloma: an unusual association with multiple sclerosis.

作者信息

John P G, Rahman J, Payne C B

机构信息

Department of Family Medicine, Wright State University School of Medicine, Dayton, Ohio 45408, USA.

出版信息

South Med J. 1995 Oct;88(10):1076-7.

PMID:7481968
Abstract

Pulmonary hyalinizing granuloma (PHG) is a rare entity included in the differential diagnosis of pulmonary nodules of unknown origin. The pathologic entity may represent a peculiar form of pulmonary immune reaction. We report the case of a 40-year-old white woman who had nodular lesions in both lung bases after a 10-year history of multiple sclerosis. An open lung biopsy was required to make the diagnosis. The association of pulmonary hyalinizing granuloma with multiple sclerosis could be coincidental, but since there is a possibility of immune reaction in the pathogenesis of both diseases, the association may be significant.

摘要

肺透明变性肉芽肿(PHG)是一种罕见的疾病,在不明原因的肺结节鉴别诊断中需要考虑。该病理实体可能代表一种特殊形式的肺免疫反应。我们报告一例40岁白人女性病例,该患者在患多发性硬化症10年后双肺底部出现结节性病变。需要进行开胸肺活检以明确诊断。肺透明变性肉芽肿与多发性硬化症的关联可能是巧合,但由于两种疾病的发病机制都有可能存在免疫反应,这种关联可能具有重要意义。

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