Department of Pulmonology, Rijnstate Hospital Arnhem, Wagnerlaan 55, 6815 AD, Arnhem, The Netherlands.
Department of Human Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, De Boelelaan 1118, 1081 HZ, Amsterdam, The Netherlands.
BMC Pulm Med. 2022 Aug 26;22(1):325. doi: 10.1186/s12890-022-02107-7.
Birt-Hogg-Dubé syndrome (BHD) is an inherited disease caused by pathogenic variants in the FLCN gene. One of the characteristics is the increased risk for spontaneous pneumothorax, likely due to the presence of pulmonary cysts mainly distributed under the carina. Due to variable expression and lack of awareness, BHD is likely to be underdiagnosed. We aimed to examine the prevalence of BHD in patients presenting with an apparent primary spontaneous pneumothorax and to evaluate the contribution of chest CT in establishing the diagnosis.
Patients who presented with apparent primary spontaneous pneumothorax between 2004 and 2017 in a large Dutch teaching hospital were enrolled in this quantitative cross-sectional study. A questionnaire was sent to eligible patients. Patients who completed the questionnaire and consented to further participation were invited to visit the hospital for genetic testing and low dose, volumetric chest CT.
Genetic testing was performed in 88 patients with apparent primary spontaneous pneumothorax. Three patients were found to have a pathogenic variant in the FLCN gene (3.4%). No variants of unknown significance were detected. Pulmonary cysts were detected in 14 out of 83 participants with an available chest CT, six had more than one cyst. All three patients with BHD had multiple pulmonary cysts.
Based on previous literature and the present study, we believe that performing a chest CT in every patient presenting with primary spontaneous pneumothorax is justified. Subsequent genetic testing of the FLCN gene should be considered when multiple pulmonary cysts are present.
The study was registered at clinicaltrials.gov with reference NCT02916992. Three out of 88 patients with an apparent primary spontaneous pneumothorax were diagnosed with Birt-Hogg-Dubé syndrome in this study and all three had multiple pulmonary cysts. We believe that performing a chest CT in every patient with an apparent primary spontaneous pneumothorax is justified to identify underlying diseases.
Birt-Hogg-Dubé 综合征(BHD)是一种由 FLCN 基因突变引起的遗传性疾病。其特征之一是自发性气胸的风险增加,这可能是由于隆突下主要分布的肺大疱。由于表现多样且缺乏认识,BHD 可能被漏诊。我们旨在研究表现为明显特发性自发性气胸的患者中 BHD 的患病率,并评估胸部 CT 在确立诊断中的作用。
本研究为一项定量的横断面研究,纳入了 2004 年至 2017 年期间在荷兰一所大型教学医院就诊的表现为明显特发性自发性气胸的患者。向符合条件的患者发送问卷。完成问卷并同意进一步参与的患者被邀请到医院进行基因检测和低剂量、容积式胸部 CT 检查。
对 88 例表现为明显特发性自发性气胸的患者进行了基因检测。在 3 例患者中发现了 FLCN 基因突变(3.4%)。未发现意义未明的变异。在可进行胸部 CT 检查的 83 名参与者中有 14 名发现了肺大疱,其中 6 名有多个肺大疱。所有 3 例 BHD 患者均有多个肺大疱。
根据既往文献和本研究,我们认为对所有特发性自发性气胸患者进行胸部 CT 检查是合理的。当存在多个肺大疱时,应考虑对 FLCN 基因进行后续基因检测。
本研究在 clinicaltrials.gov 上注册,参考号为 NCT02916992。在这项研究中,3 例表现为明显特发性自发性气胸的患者被诊断为 Birt-Hogg-Dubé 综合征,他们均有多个肺大疱。我们认为,对所有表现为明显特发性自发性气胸的患者进行胸部 CT 检查是合理的,可以识别潜在疾病。