Results 61 to 70 of about 54,323 (280)

Histological features and survival in idiopathic pulmonary fibrosis [PDF]

, 2003
BACKGROUND: Idiopathic pulmonary fibrosis was recently redefined as usual interstitial pneumonia of unknown etiology. Consequently, the prognostic value of histological findings needs to be reassessed.
Coletta, Ester Nei Aparecida Martins, Ferreira, Rimarcs Gomes, Nunes, Tatiana Santos Malheiros, Pereira, Carlos Alberto de Castro, Rubin, Adalberto Sperb, Stávale, João Norberto, Villela, Lucimara Sonja   +6 more
core   +2 more sources

Comorbid Conditions in Idiopathic Pulmonary Fibrosis: Recognition and Management. [PDF]

, 2017
Idiopathic pulmonary fibrosis (IPF), a fibrosing interstitial pneumonia of unknown etiology, primarily affects older adults and leads to a progressive decline in lung function and quality of life.
Collard, Harold R, Oldham, Justin M
core   +2 more sources

Interstitial lung disease in a female patient with rheumatoid arthritis

Современная ревматология, 2014
Rheumatoid arthritis (RA) is a progressive disease, resulting in joint deformation and development of severe functional disorders. Meanwhile, RA patients frequently have systemic inflammatory disorders of internal organs, which may significantly worsen ...
Yuliya Valeryavna Averkieva, T A Raskina, O S Malyshenko, M A Volykova, O M Maslova   +4 more
doaj   +1 more source

Fibrosing pneumonia – how to diagnose, and how to recognize the etiology?

Surgical and Experimental Pathology, 2020
Background Fibrosing pneumonias are a group of interstitial lung diseases with a different etiologic background and divergent prognosis. They are differentiated into usual interstitial pneumonia (UIP), non-specific interstitial pneumonia (NSIP), and ...
Helmut H.- Popper
doaj   +1 more source

Pulmonary vasospasm in systemic sclerosis: noninvasive techniques for detection [PDF]

, 2014
In a subgroup of patients with systemic sclerosis (SSc), vasospasm affecting the pulmonary circulation may contribute to worsening respiratory symptoms, including dyspnea.
Giannarou, S, Hansell, DM, Keir, GJ, MacDonald, P, Nair, A, Oldershaw, P, Wells, AU, Wort, SJ, Yang, G-Z   +8 more
core   +1 more source

Evaluation of the histological parameters in usual interstitial pneumonia (idiopathic pulmonary fibrosis) [PDF]

, 2000
Idiopathic pulmonary fibrosis (cryptogenic fibrosing alveolitis) is a progressive interstitial pulmonary disease of unknown etiology. Since Hamman's and Rich's (1944) reports, many studies have tried to find a histological marker for the correlation ...
Coletta, Ester Nei Aparecida Martins, Ferreira, Rimarcs Gomes, Giannotti Filho, Osvaldo   +2 more
core   +3 more sources

Serum Metabolomic Profiling in Rheumatoid Arthritis Patients With Interstitial Lung Disease: A Case–Control Study

Frontiers in Medicine, 2020
Objectives: Interstitial lung disease (ILD) is an extra-articular manifestation in rheumatoid arthritis (RA), detected in 10.7% of patients, and causing a poor prognosis. Hence, biomarkers for ILD are urgently required in RA.
Hiroshi Furukawa, Hiroshi Furukawa, Shomi Oka, Shomi Oka, Kota Shimada, Kota Shimada, Akira Okamoto, Atsushi Hashimoto, Atsushi Hashimoto, Akiko Komiya, Akiko Komiya, Koichiro Saisho, Koichiro Saisho, Norie Yoshikawa, Masao Katayama, Toshihiro Matsui, Toshihiro Matsui, Naoshi Fukui, Kiyoshi Migita, Kiyoshi Migita, Shigeto Tohma, Shigeto Tohma   +21 more
doaj   +1 more source

Sjögren Syndrome Complicated by Mucosa-Associated Lymphoid Tissue Lymphoma and Lymphocytic Interstitial Pneumonia. [PDF]

, 2015
Sjögren syndrome (SS) is an autoimmune disease with exocrine glands dysfunction and multiorgan involvement. It is associated with increased risk of lymphoproliferative disorders, especially B-cell marginal zone lymphoma.
Ahmed, Fatma, Marwaha, Nitin, Muzaffar, Razi, Osman, Medhat M, Parkar, Nadeem, Raslan, Osama   +5 more
core   +4 more sources

Esclerose sistémica progressiva – Um caso clínico

Revista Portuguesa de Pneumologia, 2002
RESUMO: A esclerose sistémica é uma doença relativamente rara sendo a terceira doença mais frequente do tecido conjuntivo, logo após a artrite rewnatoide e o lupus eritematoso sistemico. A sua forma de apresentação é variada e depende dos órgão
Inês Vicente, Eduardo Silva, Deolinda Portelinha, Manuela Meruje, Rui Pato   +4 more
doaj   +1 more source

Morphological and molecular motifs of fibrosing pulmonary injury patterns

The Journal of Pathology: Clinical Research, 2019
Interstitial lung diseases encompass a large number of entities, which are characterised by a small number of partially overlapping fibrosing injury patterns, either alone or in combination.
Danny Jonigk, Helge Stark, Peter Braubach, Lavinia Neubert, Hoen‐oh Shin, Nicole Izykowski, Tobias Welte, Sabina Janciauskiene, Gregor Warnecke, Axel Haverich, Mark Kuehnel, Florian Laenger   +11 more
doaj   +1 more source