Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
Intervalo de ano de publicação
1.
Orphanet J Rare Dis ; 15(1): 120, 2020 05 24.
Artigo em Inglês | MEDLINE | ID: mdl-32448321

RESUMO

BACKGROUND: Birt-Hogg-Dubé syndrome (BHD) is a rare autosomal dominant disorder caused by mutations in the FLCN gene coding for folliculin. Its clinical expression includes cutaneous fibrofolliculomas, renal tumors, multiple pulmonary cysts, and recurrent spontaneous pneumothoraces. Data on lung function in BHD are scarce and it is not known whether lung function declines over time. We retrospectively assessed lung function at baseline and during follow-up in 96 patients with BHD. RESULTS: Ninety-five percent of BHD patients had multiple pulmonary cysts on computed tomography and 59% had experienced at least one pneumothorax. Mean values of forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC), FEV1/FVC ratio, and total lung capacity were normal at baseline. Mean (standard deviation) residual volume (RV) was moderately increased to 116 (36) %pred at baseline, and RV was elevated > 120%pred in 41% of cases. Mean (standard deviation) carbon monoxide transfer factor (DLco) was moderately decreased to 85 (18) %pred at baseline, and DLco was decreased < 80%pred in 33% of cases. When adjusted for age, gender, smoking and history of pleurodesis, lung function parameters did not significantly decline over a follow-up period of 6 years. CONCLUSIONS: Cystic lung disease in BHD does not affect respiratory function at baseline except for slightly increased RV and reduced DLco. No significant deterioration of lung function occurs in BHD over a follow-up period of 6 years.


Assuntos
Síndrome de Birt-Hogg-Dubé , Pneumopatias , Pneumotórax , Síndrome de Birt-Hogg-Dubé/genética , Criança , Humanos , Pulmão , Pneumopatias/genética , Pneumotórax/genética , Estudos Retrospectivos
2.
Rev Med Suisse ; 9(407): 2142-4, 2146-9, 2013 Nov 20.
Artigo em Francês | MEDLINE | ID: mdl-24354248

RESUMO

During pregnancy several adaptations develop in response to the enhanced maternal and fetal metabolic needs. This review summarizes the major cardiorespiratory modifications of pregnancy as well as their consequences in chronic respiratory diseases such as restrictive ventilatory defects (post-tuberculosis pneumonectomy, kyphoscoliosis, neuromuscular disorders), asthma, cystic fibrosis, and pulmonary hypertension. It is important to recognize early the cardiorespiratory situations for which pregnancy is contraindicated or associated with a high risk of respiratory complications. Clinical management by an expert and often pluridisciplinary team is recommended.


Assuntos
Pulmão/metabolismo , Complicações na Gravidez/fisiopatologia , Doenças Respiratórias/fisiopatologia , Feminino , Humanos , Pulmão/fisiopatologia , Equipe de Assistência ao Paciente , Gravidez , Complicações na Gravidez/terapia , Doenças Respiratórias/complicações , Doenças Respiratórias/terapia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA