Results 1 to 10 of about 54,323 (280)

Usual interstitial pneumonia. [PDF]

Pan Afr Med J, 2022
This clinical scenario includes a male, aged 83 years, a retired railway worker with complaints of breathlessness (modified Medical Research Council scale grade V), cough with expectorations (thick yellow-colored), and chest pain (sudden in onset, gradually progressive, and retrosternal in nature).
Badjate DM, Jain M.
europepmc   +7 more sources

The usual Interstitial pneumonia pattern in autoimmune rheumatic diseases [PDF]

BMC Pulmonary Medicine, 2023
Usual Interstitial Pneumonia (UIP) is characterized by progression of lung parenchyma that may be observed in various autoimmune rheumatic diseases (ARDs), including rheumatoid arthritis and connective tissue diseases.
Fabrizio Luppi, Andreina Manfredi, Paola Faverio, Michael Brun Andersen, Francesca Bono, Fabio Pagni, Carlo Salvarani, Elisabeth Bendstrup, Marco Sebastiani   +8 more
doaj   +3 more sources

CT-based lung motion differences in patients with usual interstitial pneumonia and nonspecific interstitial pneumonia [PDF]

Frontiers in Physiology, 2022
We applied quantitative CT image matching to assess the degree of motion in the idiopathic ILD such as usual interstitial pneumonia (UIP) and nonspecific interstitial pneumonia (NSIP). Twenty-one normal subjects and 42 idiopathic ILD (31 UIP and 11 NSIP)
Jiwoong Choi, Jiwoong Choi, Jiwoong Choi, Kum Ju Chae, Gong Yong Jin, Ching-Long Lin, Ching-Long Lin, Ching-Long Lin, Archana T. Laroia, Eric A. Hoffman, Chang Hyun Lee, Chang Hyun Lee   +11 more
doaj   +3 more sources

A Deep Learning-Based Radiomic Classifier for Usual Interstitial Pneumonia. [PDF]

Chest, 2023
Chung JH, Chelala L, Pugashetti JV, Wang JM, Adegunsoye A, Matyga AW, Keith L, Ludwig K, Zafari S, Ghodrati S, Ghasemiesfe A, Guo H, Soo E, Lyen S, Sayer C, Hatt C, Oldham JM.   +16 more
europepmc   +4 more sources

Molecular markers of telomere dysfunction and senescence are common findings in the usual interstitial pneumonia pattern of lung fibrosis. [PDF]

Histopathology, 2021
Idiopathic pulmonary fibrosis (IPF) is a genetically mediated, age‐associated, progressive form of pulmonary fibrosis characterised pathologically by a usual interstitial pneumonia (UIP) pattern of fibrosis.
Lee JS, La J, Aziz S, Dobrinskikh E, Brownell R, Jones KD, Achtar-Zadeh N, Green G, Elicker BM, Golden JA, Matthay MA, Kukreja J, Schwartz DA, Wolters PJ.   +13 more
europepmc   +4 more sources

Lung cancer resection in patients with underlying usual interstitial pneumonia: a meta-analysis. [PDF]

BMJ Open Respir Res, 2023
Objective Patients with lung cancer with underlying idiopathic pulmonary fibrosis and usual interstitial pneumonia (UIP) pattern on CT represent a very high-risk group in terms of postoperative UIP acute exacerbations (AEs) and in-hospital mortality.
Patel AJ, Walters GI, Watkins S, Rogers V, Fallouh H, Kalkat M, Naidu B, Bishay ES.   +7 more
europepmc   +2 more sources

Interstitial lung disease progression after genomic usual interstitial pneumonia testing. [PDF]

Eur Respir J, 2023
Background A genomic classifier for usual interstitial pneumonia (gUIP) has been shown to predict histological UIP with high specificity, increasing diagnostic confidence for idiopathic pulmonary fibrosis (IPF).
Chaudhary S, Weigt SS, Ribeiro Neto ML, Benn BS, Pugashetti JV, Keith R, Chand A, Oh S, Kheir F, Ramalingam V, Solomon JJ, Harper R, Lasky JA, Oldham JM.   +13 more
europepmc   +2 more sources

MUC5B promoter variant rs35705950, rare but significant susceptibility locus in rheumatoid arthritis-interstitial lung disease with usual interstitial pneumonia in Asian populations. [PDF]

RMD Open, 2022
Background MUC5B variant rs35705950 is the common and most significant risk variant for rheumatoid arthritis-interstitial lung disease (RA-ILD) in Western populations.
Joo YB, Ahn SM, Bang SY, Park Y, Hong SJ, Lee Y, Cho SK, Choi CB, Sung YK, Kim TH, Jun JB, Yoo DH, Bae SC, Lee HS.   +13 more
europepmc   +2 more sources

A Handcrafted Radiomics-Based Model for the Diagnosis of Usual Interstitial Pneumonia in Patients with Idiopathic Pulmonary Fibrosis. [PDF]

J Pers Med, 2022
The most common idiopathic interstitial lung disease (ILD) is idiopathic pulmonary fibrosis (IPF). It can be identified by the presence of usual interstitial pneumonia (UIP) via high-resolution computed tomography (HRCT) or with the use of a lung biopsy.
Refaee T, Bondue B, Van Simaeys G, Wu G, Yan C, Woodruff HC, Goldman S, Lambin P.   +7 more
europepmc   +2 more sources

Probable usual interstitial pneumonia pattern on chest CT: is it sufficient for a diagnosis of idiopathic pulmonary fibrosis? [PDF]

European Respiratory Journal, 2020
Recent studies have suggested that in patients with an idiopathic interstitial pneumonia (IIP), a probable usual interstitial pneumonia (UIP) pattern on chest computed tomography (CT) is sufficient to diagnose idiopathic pulmonary fibrosis (IPF) without ...
Jun Fukihara, Yasuhiro Kondoh, Kevin K. Brown, Tomoki Kimura, Kensuke Kataoka, Toshiaki Matsuda, Yasuhiko Yamano, Atsushi Suzuki, Taiki Furukawa, Hiromitsu Sumikawa, Osamu Takahashi, Takeshi Johkoh, Tomonori Tanaka, Junya Fukuoka, Naozumi Hashimoto, Yoshinori Hasegawa   +15 more
openalex   +2 more sources