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原发性干燥综合征患者的缩窄性细支气管炎。

Constrictive Bronchiolitis in Patients With Primary Sjögren Syndrome.

机构信息

From the Department of Internal Medicine and.

Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN.

出版信息

J Clin Rheumatol. 2019 Mar;25(2):74-77. doi: 10.1097/RHU.0000000000000771.

DOI:10.1097/RHU.0000000000000771
PMID:29596206
Abstract

OBJECTIVE

Constrictive bronchiolitis (CB) is a poorly understood pulmonary manifestation of primary Sjögren syndrome (pSS). We aimed to clarify the presenting clinicoradiologic features and clinical course of pSS-associated CB through a retrospective cohort study.

METHODS

We retrospectively identified 11 patients with pSS and CB (defined by mosaic pattern with air trapping on computed tomography) encountered at our institution over 9 years from 2007 to 2015. Presenting clinical features, laboratory results, radiologic findings, and clinical course were analyzed.

RESULTS

Our patients were mostly women (91%), with a median age 53 years (range, 31-76 years) at the time of pulmonary symptom (dyspnea or cough) onset. Most (64%) were nonsmokers. Average interval between diagnosis of pSS and the onset of pulmonary symptoms was 4.4 years; in 4 patients (36%), CB was the presenting manifestation of pSS. Chest radiographs were normal (67%) or demonstrated hyperinflation (33%). Pulmonary function testing demonstrated airflow obstruction in 7 patients (63%), and 2 patients (18%) had an isolated reduction in diffusing capacity, whereas the remaining 2 patients manifested mixed physiology or normal results. Surgical lung biopsy was performed in 2 patients and confirmed the diagnosis of CB in both. Treatment was variable among our patients included glucocorticoids, hydroxychloroquine, mycophenolate mofetil, and cyclophosphamide. Among 6 patients with follow-up computed tomography and pulmonary function, the results remained stable or worsened.

CONCLUSIONS

Constrictive bronchiolitis is a rare extraglandular manifestation and can sometimes be the presenting manifestation of pSS. This pulmonary manifestation is associated with an indolent clinical course and does not respond well to immunosuppressive therapy.

摘要

目的

缩窄性细支气管炎(CB)是原发性干燥综合征(pSS)一种尚未被充分认识的肺部表现。我们旨在通过回顾性队列研究阐明 pSS 相关 CB 的临床表现和放射学特征以及临床病程。

方法

我们回顾性地确定了 2007 年至 2015 年 9 年间在我院发现的 11 例患有 pSS 和 CB(定义为 CT 上有马赛克模式伴空气潴留)的患者。分析了患者的临床表现、实验室结果、放射学发现和临床病程。

结果

我们的患者大多为女性(91%),在出现肺部症状(呼吸困难或咳嗽)时的中位年龄为 53 岁(范围为 31-76 岁)。大多数患者(64%)为不吸烟者。pSS 诊断与肺部症状出现之间的平均间隔为 4.4 年;4 例患者(36%)以 CB 为 pSS 的首发表现。胸部 X 线片正常(67%)或显示过度充气(33%)。7 例患者(63%)存在气流阻塞性肺功能障碍,2 例患者(18%)单纯弥散能力下降,其余 2 例患者表现为混合性生理学或正常结果。2 例患者进行了外科肺活检,均证实为 CB。我们的患者接受的治疗各不相同,包括糖皮质激素、羟氯喹、霉酚酸酯和环磷酰胺。在 6 例具有随访 CT 和肺功能的患者中,结果保持稳定或恶化。

结论

缩窄性细支气管炎是一种罕见的腺外表现,有时可作为 pSS 的首发表现。这种肺部表现与慢性临床病程相关,且对免疫抑制治疗反应不佳。

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