Conţinutul numărului revistei |
Articolul precedent |
Articolul urmator |
910 12 |
Ultima descărcare din IBN: 2023-03-05 11:12 |
Căutarea după subiecte similare conform CZU |
616.23/.24-003.4-073:575 (1) |
Patologia sistemului respirator. Tulburări ale organelor de respiraţie (757) |
Genetică generală. Citogenetică generală (427) |
SM ISO690:2012 ŞCIUCA, Svetlana, GUDUMAC, Eva, SELEVESTRU, Rodica, BALANEŢCHI, Ludmila, CRIVCEANSCHI, Maxim, CRIVCEANSCHI, Eugenia. Modificări imagistice pulmonare în fibroza chistică. In: Buletin de Perinatologie, 2016, nr. 4(72), pp. 22-25. ISSN 1810-5289. |
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Buletin de Perinatologie | |||||||
Numărul 4(72) / 2016 / ISSN 1810-5289 | |||||||
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CZU: 616.23/.24-003.4-073:575 | |||||||
Pag. 22-25 | |||||||
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Rezumat | |||||||
Cystic fibrosis is a hereditary disease which the clinical triad: chronic lung disease (chronic coughing with purulent expectoration, dyspnoea, cyanosis), exocrine pancreatic insufficiency with maldigestion and malabsorbtion (high degree of fat in faeces, fetid, high quantity), high chlorid levels in sweat. In this work there were evaluated the peculiarities of lung anatomo-morphological substrate in 50 patients with cystic fibrosis by spiral computed tomography. Tomography scans showed the presence of severe changes of lung parenchyma in the most of cases such as broshiectasis, focal or diffuse fibrosis, air- fluid level cysts, and signs of chronic bronchopulmonary process. |
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