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Birt-Hogg-Dubé syndrome presenting with spontaneous pneumothorax and extensive pulmonary cysts in the absence of skin lesions or renal pathology.Birt-Hogg-Dubé综合征表现为自发性气胸和广泛的肺囊肿,而无皮肤病变或肾脏病理改变。
BMJ Case Rep. 2019 Sep 6;12(9):e231039. doi: 10.1136/bcr-2019-231039.
2
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Delayed diagnosis of Birt-Hogg-Dubé syndrome due to marked intrafamilial clinical variability: a case report.因家族内临床表现明显差异而导致的伯特-霍格-杜布综合征延迟诊断:病例报告。
BMC Med Genet. 2018 Mar 16;19(1):45. doi: 10.1186/s12881-018-0558-0.
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Birt-Hogg-Dubé syndrome: diagnosis and management.Birt-Hogg-Dubé 综合征:诊断与管理。
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Birt-Hogg-Dubé syndrome.Birt-Hogg-Dubé 综合征。
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Birt-Hogg-Dubé syndrome - a rare genetic disorder complicated by pneumothorax: A case report.Birt-Hogg-Dubé综合征——一种并发气胸的罕见遗传性疾病:病例报告
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Comment on Balsamo et al.: "Birt-Hogg-Dubé syndrome with simultaneous hyperplastic polyposis of the gastrointestinal tract: case report and review of the literature".关于巴尔萨莫等人的评论:“伴有胃肠道同时性增生性息肉病的Birt-Hogg-Dubé综合征:病例报告及文献综述”
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A systematic review assessing the existence of pneumothorax-only variants of FLCN. Implications for lifelong surveillance of renal tumours.系统评价评估有无仅存在气胸的常染色体显性遗传多囊肾病(FLCN)变异型。对肾肿瘤终身监测的影响。
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本文引用的文献

1
Familial pneumothorax: towards precision medicine.家族性气胸:迈向精准医学。
Thorax. 2018 Mar;73(3):270-276. doi: 10.1136/thoraxjnl-2017-211169. Epub 2017 Dec 28.
2
Novel clinical scoring system to identify patients with pneumothorax with suspicion for Birt-Hogg-Dubé syndrome.新型临床评分系统,用于识别疑似 Birt-Hogg-Dubé 综合征的气胸患者。
Respirology. 2018 Apr;23(4):414-418. doi: 10.1111/resp.13191. Epub 2017 Sep 27.
3
Diffuse cystic lung diseases: differential diagnosis.弥漫性囊性肺疾病:鉴别诊断
J Bras Pneumol. 2017 Mar-Apr;43(2):140-149. doi: 10.1590/S1806-37562016000000341.
4
Birt-Hogg-Dubé syndrome: a case report and a review of the literature.Birt-Hogg-Dubé综合征:一例病例报告及文献综述
Eur Clin Respir J. 2017 Feb 20;4(1):1292378. doi: 10.1080/20018525.2017.1292378. eCollection 2017.
5
H255Y and K508R missense mutations in tumour suppressor folliculin (FLCN) promote kidney cell proliferation.肿瘤抑制因子卵泡抑素(FLCN)中的H255Y和K508R错义突变促进肾细胞增殖。
Hum Mol Genet. 2017 Jan 15;26(2):354-366. doi: 10.1093/hmg/ddw392.
6
Molecular genetics and clinical features of Birt-Hogg-Dubé syndrome.Birt-Hogg-Dubé综合征的分子遗传学与临床特征
Nat Rev Urol. 2015 Oct;12(10):558-69. doi: 10.1038/nrurol.2015.206. Epub 2015 Sep 1.
7
Diagnosis and management of BHD-associated kidney cancer.BHD 相关性肾癌的诊断与治疗。
Fam Cancer. 2013 Sep;12(3):397-402. doi: 10.1007/s10689-013-9657-4.
8
Birt-Hogg-Dube syndrome: clinicopathological features of the lung.Birt-Hogg-Dube 综合征:肺部的临床病理特征。
J Clin Pathol. 2013 Mar;66(3):178-86. doi: 10.1136/jclinpath-2012-201200. Epub 2012 Dec 8.
9
Renal cancer and pneumothorax risk in Birt-Hogg-Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families.Birt-Hogg-Dubé 综合征中肾癌和气胸的风险:35 个 BHD 家族 115 名 FLCN 突变携带者的分析。
Br J Cancer. 2011 Dec 6;105(12):1912-9. doi: 10.1038/bjc.2011.463.
10
Birt-Hogg-Dubé syndrome: diagnosis and management.Birt-Hogg-Dubé 综合征:诊断与管理。
Lancet Oncol. 2009 Dec;10(12):1199-206. doi: 10.1016/S1470-2045(09)70188-3.

Birt-Hogg-Dubé综合征表现为自发性气胸和广泛的肺囊肿,而无皮肤病变或肾脏病理改变。

Birt-Hogg-Dubé syndrome presenting with spontaneous pneumothorax and extensive pulmonary cysts in the absence of skin lesions or renal pathology.

作者信息

Kumar Kartik, Ross Clare

机构信息

Department of Respiratory Medicine, St Mary's Hospital, Imperial College Healthcare NHS Trust, London, UK.

出版信息

BMJ Case Rep. 2019 Sep 6;12(9):e231039. doi: 10.1136/bcr-2019-231039.

DOI:10.1136/bcr-2019-231039
PMID:31494588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6731778/
Abstract

Birt-Hogg-Dubé (BHD) syndrome is an autosomal dominant condition which classically manifests with skin lesions such as fibrofolliculomas, pulmonary cysts that predispose to spontaneous pneumothorax and an increased risk of developing renal cell carcinoma. We describe the case of a patient who presented with a spontaneous pneumothorax on a background of multiple lung cysts, in the absence of cutaneous fibrofolliculomas and renal tumours. A germline mutation in the folliculin FLCN gene was subsequently identified, confirming BHD syndrome. Our case highlights the importance of considering a broad differential diagnosis for the cause of a spontaneous pneumothorax in the presence of unexplained cystic lung disease and emphasises the value of maintaining a high index of clinical suspicion for inherited causes of pneumothoraces.

摘要

Birt-Hogg-Dubé(BHD)综合征是一种常染色体显性疾病,典型表现为皮肤病变,如纤维毛囊瘤、易导致自发性气胸的肺囊肿以及患肾细胞癌风险增加。我们描述了一例患者,该患者在存在多个肺囊肿的背景下出现自发性气胸,且无皮肤纤维毛囊瘤和肾肿瘤。随后鉴定出卵泡抑素FLCN基因的种系突变,确诊为BHD综合征。我们的病例强调了在存在不明原因的囊性肺病时,对自发性气胸病因进行广泛鉴别诊断的重要性,并强调了对气胸的遗传病因保持高度临床怀疑指数的价值。