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[Pulmonary manifestations of antisynthetase syndrome]. / Les manifestations pulmonaires du syndrome des antisynthétases.
Jouneau, S; Hervier, B; Jutant, E-M; Decaux, O; Kambouchner, M; Humbert, M; Delaval, P; Montani, D.
Afiliação
  • Jouneau S; Service de pneumologie, centre de compétences des maladies pulmonaires rares de Bretagne, hôpital Pontchaillou, 2, rue Henri-Le-Guilloux, 35033 Rennes cedex, France; IRSET UMR 1085, université de Rennes 1, Rennes, France. Electronic address: stephane.jouneau@chu-rennes.fr.
  • Hervier B; Service de médecine interne et immunologie clinique, groupe hospitalier Pitié-Salpêtrière, AP-HP-UPMC, Paris, France.
  • Jutant EM; Service de pneumologie, centre de référence de l'hypertension pulmonaire sévère, faculté de médecine, université Paris-Sud, hôpital de Bicêtre, AP-HP, département hospitalo-universitaire (DHU) Thorax Innovation (TORINO), 94270 Le-Kremlin-Bicêtre, France; UMR_S 999, université Paris-Sud, Inserm, labo
  • Decaux O; Service de médecine interne, hôpital sud, Rennes, France; UMR CNRS 6290 IGDR, université de Rennes 1, Rennes, France.
  • Kambouchner M; Service d'anatomie pathologique, hôpital Avicenne, AP-HP, Bobigny, France.
  • Humbert M; Service de pneumologie, centre de référence de l'hypertension pulmonaire sévère, faculté de médecine, université Paris-Sud, hôpital de Bicêtre, AP-HP, département hospitalo-universitaire (DHU) Thorax Innovation (TORINO), 94270 Le-Kremlin-Bicêtre, France; UMR_S 999, université Paris-Sud, Inserm, labo
  • Delaval P; Service de pneumologie, centre de compétences des maladies pulmonaires rares de Bretagne, hôpital Pontchaillou, 2, rue Henri-Le-Guilloux, 35033 Rennes cedex, France; IRSET UMR 1085, université de Rennes 1, Rennes, France.
  • Montani D; Service de pneumologie, centre de référence de l'hypertension pulmonaire sévère, faculté de médecine, université Paris-Sud, hôpital de Bicêtre, AP-HP, département hospitalo-universitaire (DHU) Thorax Innovation (TORINO), 94270 Le-Kremlin-Bicêtre, France; UMR_S 999, université Paris-Sud, Inserm, labo
Rev Mal Respir ; 32(6): 618-28, 2015 Jun.
Article em Fr | MEDLINE | ID: mdl-26231412
ABSTRACT
Antisynthetase syndrome is an inflammatory myopathy frequently associated with pulmonary manifestations, especially interstitial lung diseases, and uncommonly pulmonary hypertension. In the context of a suggestive clinical and radiological picture, positive anti-RNA synthetase antibodies confirm the diagnosis. Anti-Jo1, anti-PL7, and anti-PL12 antibodies are the more commonly encountered. The presence of a number of extra-thoracic manifestations in association with pulmonary disease may suggest the diagnosis. These include myalgia or muscular deficit, Raynaud's phenomenon, polyarthritis, fever, mechanics hands. Serum creatine kinase levels are usually increased. Electromyogram, muscular magnetic resonance imaging or muscle pathology are not mandatory to make the diagnosis. There is a high variability in symptoms and severity, between patients but also during the course of the disease in the same patient. The presence of an interstitial lung disease is a major prognostic factor and an indication for more intensive treatment, principally with systemic corticosteroids with or without immunosuppressive drugs. Improving respiratory physicians' knowledge of this disease, which is often revealed by its pulmonary manifestations, should help diagnosis, therapeutic management, and possibly prognosis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Pulmonares Intersticiais / Hipertensão Pulmonar / Miosite Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Humans Idioma: Fr Revista: Rev Mal Respir Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Pulmonares Intersticiais / Hipertensão Pulmonar / Miosite Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Humans Idioma: Fr Revista: Rev Mal Respir Ano de publicação: 2015 Tipo de documento: Article