[肉芽肿性淋巴细胞间质性肺疾病(GLILD)作为常见变异性免疫缺陷(CVID)肺部改变的表现-病例报告]。

Przeglad lekarski Pub Date : 2016-01-01
Elżbieta Marciszewska, Anna Szaflarska, Anna Pituch-Noworolska
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引用次数: 0

摘要

常见变异性免疫缺陷(CVID)包括不同种类的原发性低γ -球蛋白血症,大多病因不明。该疾病的发病及其临床症状可在儿童和成人中出现。除了对细菌、病毒和真菌感染的易感性外,还经常观察到其他临床症状(自身免疫、非感染性肺和胃肠道疾病、肿瘤)。约58%的cvid患者发展为肉芽肿性和淋巴细胞间质性肺疾病(GLILD),与早期死亡相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Granulomatous lymphocytic interstitial lung disease (GLILD) as a manifestation of pulmonary changes in common variable immunodeficiency (CVID) – case report].

Common variable immunodeficiency (CVID) comprise different kinds of primary hypogammaglobulinemias of mostly unknown etiology. The onset of the disease and its clinical symptoms may appear as well in children as in adults. Apart from susceptibility to bacterial, viral and fungal infections, other clinical signs (autoimmunization, non-infectious lung and gastrointestinal diseases, neoplasm) are frequently observed. About 58% of patients with CVID develops granulomatous and lymphocytic interstitial lung disease (GLILD) associated with early mortality.

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