Estrogen and progesterone receptors - Their role in postsclerotherapy angiogenesis telangiectatic matting (TM)

Citation
Ns. Sadick et C. Urmacher, Estrogen and progesterone receptors - Their role in postsclerotherapy angiogenesis telangiectatic matting (TM), DERM SURG, 25(7), 1999, pp. 539-542
Citations number
36
Categorie Soggetti
Dermatology
Journal title
DERMATOLOGIC SURGERY
ISSN journal
10760512 → ACNP
Volume
25
Issue
7
Year of publication
1999
Pages
539 - 542
Database
ISI
SICI code
1076-0512(199907)25:7<539:EAPR-T>2.0.ZU;2-0
Abstract
BACKGROUND. Postsclerotherapy neoangiogenesis telangiectatic matting (TM) o ccurs in up to 24% of individuals treated by sclerotherapy. Although the et iology is unknown, obstructive now factors, angiogenic factors, estrogen, i nflammatory, and endogenous factors have all been postulated to play a role in its pathogenesis. OBJECTIVE. The aim of the study was to ascertain the presence or absence of estrogen and progesterone receptors in postsclerotherapy TM lesions and th us substantiate their possible role in the pathogenesis of TM. METHODS. Ten women, median age 37.7 years, were included in the study popul ation who developed TM following a single sclerotherapy treatment session e mploying Sotradecol 0.25% for class I-II telangiectasia/venulectasia. Four of 10 patients had a history of previous hormonal therapy or pregnancy in t he previous 12 months prior to entering into the study. Three millimeter pu nch biopsies were taken at 12 weeks posttreatment and assayed for estrogen and progesterone receptors by the ERICA and ERICA (estrogen/progesterone im mune cytochemical assay) techniques. RESULTS. Zero of 10 patients were positive for estrogen/progesterone recept ors as assayed by the ERICA/PRICA technique in biopsied sites of postsclero therapy TM. CONCLUSION. Although estrogen and progesterone may play an indirect role in the development of postsclerotherapy TM via vasodilatory or secondary angi ogenic or cytokine release mechanisms, they do not appear to play a primary role in promoting postsclerotherapy neoangiogenesis as demonstrated in thi s study.