Page last updated: 2024-11-06

hydrocortisone acetate and Graft vs Host Disease

hydrocortisone acetate has been researched along with Graft vs Host Disease in 3 studies

hydrocortisone acetate: RN given refers to cpd without isomeric designation

Graft vs Host Disease: The clinical entity characterized by anorexia, diarrhea, loss of hair, leukopenia, thrombocytopenia, growth retardation, and eventual death brought about by the GRAFT VS HOST REACTION.

Research Excerpts

ExcerptRelevanceReference
"We describe five patients with vaginal stenosis that was due to chronic graft-versus-host reaction after bone marrow transplantation."1.32Treatment of vaginal outflow tract obstruction in graft-versus-host reaction. ( Haddad, B; Louis-Sylvestre, C; Paniel, BJ, 2003)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Rajkumar, S1
Lewis, F1
Nath, R1
Louis-Sylvestre, C1
Haddad, B1
Paniel, BJ1
SCHLESINGER, M1
MARK, R1

Other Studies

3 other studies available for hydrocortisone acetate and Graft vs Host Disease

ArticleYear
The importance of topical steroids after adhesiolysis in erosive lichen planus and graft versus host disease.
    Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology, 2019, Volume: 39, Issue:1

    Topics: Administration, Cutaneous; Anti-Inflammatory Agents; Clobetasol; Female; Graft vs Host Disease; Huma

2019
Treatment of vaginal outflow tract obstruction in graft-versus-host reaction.
    American journal of obstetrics and gynecology, 2003, Volume: 188, Issue:4

    Topics: Administration, Intravaginal; Administration, Topical; Adult; Anti-Inflammatory Agents; Constriction

2003
WASTING DISEASE INDUCED IN YOUNG MICE BY ADMINISTRATION OF CORTISOL ACETATE.
    Science (New York, N.Y.), 1964, Feb-28, Volume: 143, Issue:3609

    Topics: Acetates; Animals; Cachexia; Graft vs Host Disease; Hydrocortisone; Metabolic Diseases; Mice; Resear

1964