Pregled bibliografske jedinice broj: 606303
Pulmonary manifestations of connective tissue disease(CTD) ; lung invlvement as the initial sign of CTD
Pulmonary manifestations of connective tissue disease(CTD) ; lung invlvement as the initial sign of CTD // Lung in non-pulmonary and systemic disease / Peroš-Golubičić, Tatjana (ur.).
Zagreb: Medicinska naklada, 2013. str. 206-219
CROSBI ID: 606303 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Pulmonary manifestations of connective tissue disease(CTD) ; lung invlvement as the initial sign of CTD
Autori
Peroš-Golubičić, Tatjana
Vrsta, podvrsta i kategorija rada
Poglavlja u knjigama, znanstveni
Knjiga
Lung in non-pulmonary and systemic disease
Urednik/ci
Peroš-Golubičić, Tatjana
Izdavač
Medicinska naklada
Grad
Zagreb
Godina
2013
Raspon stranica
206-219
ISBN
978-953-176-577-0
Ključne riječi
connective tissue disease, pulmonary manifestations
Sažetak
Numerous connective tissue diseases (CTD) involve the lungs, but most frequently systemic sclerosis (SSc), rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), polymyositis/dermatomyositis (PM/DM), mixed connective tissue disease (MCTD) and Sjögren syndrome (SS). Many other connective tissue diseases (i.e. overlap syndromes, ankylosing spondylitis) also show number of different pulmonary manifestations. Interstitial lung disease, bronchiolitis, bronchiectasis, pleural effusion, respiratory muscle weakness, diffuse alveolar hemorrhage and pulmonary hypertension are seen. The patients with established diagnosis of connective tissue disease and lung affection are in most cases a therapeutic problem. The early recognition of these complications is important because timely and adequate, often aggressive immunosuppressive therapy is needed in order to preserve organ integrity and function. On the other hand, there is a group of patients who present as interstitial lung disease, pleural effusion, diffuse alveolar hemorrhage or bronchiolitis, as the commencing, initial sign of connective tissue disease. Here we present a group of 26 patients with interstitial lung disease in which during time, months or even years the connective tissue disease was diagnosed. Finally, there were 6 pts with SSc, five with RA, five with MCTD, four SLE, two with PM/DM, and the rest were unclassified CTD. The characteristics of clinical presentation, diagnostic procedures and prognosis are shown.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Klinika za plućne bolesti "Jordanovac"
Profili:
Tatjana Peroš-Golubičić
(autor)