نتایج جستجو برای: interstitial lung disease

تعداد نتایج: 1739449  

Journal: :Deutsches Arzteblatt international 2015
Lars Hagmeyer Winfried Randerath

BACKGROUND Smoking-related interstitial lung diseases (SR-ILDs) are a heterogeneous group of diseases with major clinical significance. Reliable epidemiological data are not yet available. METHOD Review of pertinent literature retrieved by a selective search in PubMed. RESULTS The available data on many aspects of SR-ILDs are sparse, but recent studies on the pathophysiology and targeted tr...

Journal: :Thorax 1996
D B Coultas M P Hughes

BACKGROUND The sensitivity and accuracy of death certificates and mortality data as sources of population based data on the occurrence of interstitial lung diseases has received limited attention. To determine the usefulness of these data sources, death certificates and mortality data from patients in New Mexico were examined. METHODS Patients with an interstitial lung disease were identified...

2013
Fujiko Someya Naoki Mugii

Although the relationship between muscle strength and exercise capacity has been demonstrated in dermatomyositis without lung dysfunction, little is known about the association between exercise capacity and interstitial lung disease in dermatomyositis. Eleven patients with dermatomyositis with interstitial lung disease without the manifestation of muscle weakness and 12 patients with idiopathic...

2013
Hyun Jung Kim Kyu Jin Kim Kwan Ho Lee Kyeong-Cheol Shin Jin Hong Chung Myung Soo Hyun Ki-Hong Kim

Dyskeratosis congenita is a rare congenital disorder characterized by a triad of reticular pigmentation of the skin, dystrophic nails, and leukoplakia of the mucous membrane. Sometimes it is associated with bone marrow failure, secondary malignancy and interstitial lung disease. Though it is rare, Dyskeratosis congenita is diagnosed relatively easily when clinicians suspect it. It can be diagno...

Journal: :Thorax 1969
E Cruz J Rodriguez C Lisboa R Ferretti

Desquamative interstitial pneumonia is a disease characterized by massive alveolar cell proliferation and desquamation with sparse interstitial involvement. The reported case shows an unusually widespread radiographic reticulo-nodular image and abundant alveolar cells in the sputum. Functional studies reveal the expected diffusion defect with practically normal mechanical properties of the lung...

Journal: :JAAD case reports 2016
Melissa J Danesh Drew K Saylor Lorriana E Leard Jeffrey P North Lindy P Fox

AN: acanthosis nigricans CTD: connective tissue disease ILD: interstitial lung disease NSIP: nonspecific interstitial pneumonia TP: tripe palms INTRODUCTION Tripe palms [(TP); acral acanthosis nigricans (AN)], is a rare cutaneous syndrome in which the palms develop velvety thickening and rugosity that creates an exaggeration or distortion of dermatoglyphics, resembling boiled tripe. In more tha...

Journal: :iranian red crescent medical journal 0
hakan tanriverdi department of chest diseases and tuberculosis, faculty of medicine, bulent ecevit university, zonguldak, turkey; department of chest diseases and tuberculosis, faculty of medicine, bulent ecevit university, zonguldak, turkey. tel: +90-3722612685, fax: +90-3722612001 fatma erboy department of chest diseases and tuberculosis, faculty of medicine, bulent ecevit university, zonguldak, turkey bulent altinsoy department of chest diseases and tuberculosis, faculty of medicine, bulent ecevit university, zonguldak, turkey firat uygur department of chest diseases and tuberculosis, faculty of medicine, bulent ecevit university, zonguldak, turkey mehmet arasli department of immunology, faculty of medicine, bulent ecevit university, zonguldak, turkey ishak ozel tekin department of immunology, faculty of medicine, bulent ecevit university, zonguldak, turkey

results in total, 261 patients (119 sarcoidosis and 142 non-sarcoidosis ilds) were enrolled. the median (interquartile range) bal cd4/cd8 ratio and lymphocyte fraction were significantly higher in sarcoidosis than in non-sarcoidosis ilds: 3.88 (3.76) versus 0.88 (1.01), respectively, and 20.6 (28.3) versus 6.0 (13.7), respectively. t cell receptor γ delta, cd16+56+, cd103+, cd8+103+, and cd3+16...

2005
Hyo-Bin Kim So-Yeon Lee Ja-Hyung Kim Ju-Young Jang Jooryung Huh Seong-Jong Park Soo-Jong Hong

Most of the interstitial lung diseases are rare, chronic, progressive and fatal disorders, especially in familial form. The etiology of the majority of interstitial lung disease is still unknown. Host susceptibility, genetic and environmental factors may influence clinical expression of each disease. With familial interstitial lung diseases, mutations of surfactant protein B and surfactant prot...

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