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一名既往健康的40岁女性中与原发性IgG2/IgG4缺乏相关的滤泡性细支气管炎

Follicular Bronchiolitis Associated With Primary IgG2/IgG4 Deficiency in a Previously Healthy 40-Year-Old Woman.

作者信息

Assaad Mansur, Aqeel Anam, Walsh James

机构信息

Pulmonary and Critical Care Medicine, Guthrie Robert Packer Hospital, Sayre, USA.

Internal Medicine, Guthrie Robert Packer Hospital, Sayre, USA.

出版信息

Cureus. 2022 Feb 13;14(2):e22183. doi: 10.7759/cureus.22183. eCollection 2022 Feb.

Abstract

Follicular bronchiolitis (FB) associated with immunodeficiency is not commonly reported in peer-reviewed literature. Herein, we present a case of FB associated with IgG2/IgG4 deficiency. The presence of non-specific respiratory symptoms, including cough and dyspnea with exertion, led to a CT scan of the chest, which showed diffuse, peripheral, micronodular tree-in-bud opacities and an isolated area of bronchiectasis. Despite an extensive workup, including a non-diagnostic transbronchial biopsy, no obvious etiology for the patient's clinical presentation was established, and a surgical lung biopsy was needed to confirm the diagnosis of FB. Further lab testing to evaluate for immunodeficiency confirmed an isolated deficiency in both IgG2 and IgG4. Although treating the underlying cause of FB is the standard of care, there are no established guidelines regarding standard management of FB associated with immunodeficiency, specifically IgG2/IgG4 deficiency. Therefore, a careful evaluation for immunodeficiency should be considered when evaluating for the underlying etiology of FB, as management options differ depending on the underlying diagnosis.

摘要

与免疫缺陷相关的滤泡性细支气管炎(FB)在同行评审文献中并不常见。在此,我们报告一例与IgG2/IgG4缺乏相关的FB病例。非特异性呼吸道症状的出现,包括咳嗽和劳力性呼吸困难,导致进行胸部CT扫描,结果显示弥漫性、外周性、微结节状的树芽征样混浊以及一个孤立的支气管扩张区域。尽管进行了广泛的检查,包括未得出诊断结果的经支气管活检,但仍未确定该患者临床表现的明显病因,需要进行外科肺活检以确诊FB。进一步的实验室检测以评估免疫缺陷,证实存在IgG2和IgG4的孤立性缺乏。虽然治疗FB的潜在病因是标准治疗方法,但对于与免疫缺陷相关的FB,特别是IgG2/IgG4缺乏,尚无既定的标准管理指南。因此,在评估FB的潜在病因时,应考虑对免疫缺陷进行仔细评估,因为管理方案会因潜在诊断的不同而有所差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02bb/8923243/b8d7615b3df6/cureus-0014-00000022183-i01.jpg

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