Page last updated: 2024-10-30

mechlorethamine and Idiopathic Pulmonary Fibrosis

mechlorethamine has been researched along with Idiopathic Pulmonary Fibrosis in 1 studies

nitrogen mustard : Compounds having two beta-haloalkyl groups bound to a nitrogen atom, as in (X-CH2-CH2)2NR.

Idiopathic Pulmonary Fibrosis: A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (100.00)2.80

Authors

AuthorsStudies
Solopov, P1
Colunga Biancatelli, RML1
Dimitropoulou, C1
Catravas, JD1

Other Studies

1 other study available for mechlorethamine and Idiopathic Pulmonary Fibrosis

ArticleYear
Sex-Related Differences in Murine Models of Chemically Induced Pulmonary Fibrosis.
    International journal of molecular sciences, 2021, May-31, Volume: 22, Issue:11

    Topics: Animals; Collagen; Female; Gene Expression Regulation; HSP90 Heat-Shock Proteins; Humans; Hydrochlor

2021