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一名患有常见可变免疫缺陷综合征患者的肺黏膜相关淋巴组织淋巴瘤。

Pulmonary mucosa-associated lymphoid tissue lymphoma in a patient with common variable immunodeficiency syndrome.

作者信息

Reichenberger F, Wyser C, Gonon M, Cathomas G, Tamm M

机构信息

Division of Pneumology, Department of Internal Medicine, University Hospital, Basel, Switzerland.

出版信息

Respiration. 2001;68(1):109-12. doi: 10.1159/000050475.

Abstract

Common variable immunodeficiency syndrome (CVID) is a primary immunodeficiency typically presenting with recurrent sinopulmonary infections. Non-Hodgkin's lymphoma and other secondary cancers are typical late complications of CVID. We report on a patient suffering from CVID with a history of recurrent sinopulmonary infections, interstitial pulmonary changes and hepatic granulomas. Despite treatment with intravenous immunoglobulin followed by a reduction in the number of pulmonary infections, reticular and nodular lung changes progressed. Video-assisted thoracoscopic lung biopsy showed a low-grade B cell lymphoma of the mucosa-associated lymphoid tissue (MALT) of the bronchus without evidence of pulmonary infection. In conclusion, MALT lymphoma of the lung should be considered in the differential diagnosis of progressive lung disease in CVID.

摘要

普通可变型免疫缺陷综合征(CVID)是一种原发性免疫缺陷病,通常表现为反复的鼻窦肺部感染。非霍奇金淋巴瘤和其他继发性癌症是CVID典型的晚期并发症。我们报告了一名患有CVID的患者,有反复鼻窦肺部感染、间质性肺部改变和肝肉芽肿病史。尽管接受了静脉注射免疫球蛋白治疗,随后肺部感染次数减少,但网状和结节状肺部改变仍有进展。电视辅助胸腔镜肺活检显示支气管黏膜相关淋巴组织(MALT)的低度B细胞淋巴瘤,无肺部感染证据。总之,在CVID患者出现进行性肺部疾病的鉴别诊断中应考虑肺MALT淋巴瘤。

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