Prevalence and recurrence rates of spontaneous pneumothorax in patients with diffuse cystic lung diseases in China.

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY Orphanet Journal of Rare Diseases Pub Date : 2025-02-11 DOI:10.1186/s13023-025-03587-6
Rui Wang, Xianmeng Chen, Shicheng Xu, Xianliang Jiang, Jinli Liu, Xuehan Liu, Jay H Ryu, Xiaowen Hu
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Abstract

Objectives: To investigate the prevalence and recurrence rates of spontaneous pneumothorax (SP) in patients with diffuse cystic lung diseases (DCLDs).

Methods: We retrospectively identified and analyzed medical records of patients with DCLDs encountered at the First Affiliated Hospital of University of Science and Technology of China from Jan 1, 2017 to December 31, 2023.

Results: A total of 289 patients were identified with DCLDs; 212 females and 77 males, with a median age of 48 years (range, 18-81 years). Among them, 89 (31%) patients had experienced SP; 59% among 115 patients with Birt-Hogg-Dubé (BHD), 34% of 41 patients with lymphangioleiomyomatosis (LAM, all women), 36% of 11 patients with pulmonary Langerhans cell histiocytosis (PLCH), none of 57 patients with Sjögren's syndrome-associated diffuse cystic lung disease (SS-DCLD), and 5% of 65 patients with no identifiable underlying disease (χ² = 90.585, P < 0.001). The overall recurrence rate of SP was higher with observation or chest tube placement strategy compared to surgical intervention, 59% vs. 11% (P < 0.001, 95% CI [0.1, -0.4]), respectively. The recurrence rate after surgical management was significantly lower compared to conservative management in patients with BHD (10% vs. 69%, P < 0.001, 95% CI [0.1, 0.3]) and LAM (20% vs. 57%, P = 0.322, 95% CI [0.1, 2.1]). Among patients with BHD, LAM, and PLCH, those who had pneumothorax as the initial presentation were diagnosed of their underlying disease at a significantly younger age (42.2 ± 13.0 years) compared to those without pneumothorax (48.1 ± 11.8 years) (P = 0.032, 95% CI [-8.24, -0.36]). Notably, eight of LAM patients who were treated with sirolimus after the initial SP did not experience recurrence of SP.

Conclusion: The risk of SP secondary to DCLDs was highest in patients with BHD, followed by those with PLCH and LAM. It was extremely low in SS-DCLD. Pneumothorax as the initial presentation often facilitated diagnosis of the underlying disease. Surgical treatment was associated with a lower recurrence rate of SP compared to nonsurgical management. In addition, sirolimus therapy may reduce the risk of pneumothorax recurrence in patients with LAM.

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中国弥漫性囊性肺疾病患者自发性气胸的患病率及复发率
目的:探讨弥漫性囊性肺疾病(DCLDs)患者自发性气胸(SP)的患病率及复发率。方法:回顾性分析2017年1月1日至2023年12月31日在中国科学技术大学第一附属医院就诊的DCLDs患者的病历。结果:289例患者被确诊为DCLDs;女性212人,男性77人,中位年龄48岁(范围18-81岁)。其中89例(31%)患者发生过SP;115例birt - hogg - dub (BHD)患者中有59%,41例淋巴管扁平肌瘤病(LAM,均为女性)中有34%,11例肺朗格汉斯细胞组织细胞增多症(PLCH)中有36%,57例Sjögren综合征相关弥漫性囊性肺疾病(SS-DCLD)中无,65例无可识别基础疾病的患者中有5% (χ²= 90.585,P)结论:BHD患者继发于DCLDs的SP风险最高,PLCH和LAM患者次之。在ss - dld中极低。气胸作为最初的表现往往有助于诊断潜在的疾病。与非手术治疗相比,手术治疗与较低的SP复发率相关。此外,西罗莫司治疗可降低LAM患者气胸复发的风险。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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