Electronic brachytherapy management of atypical fibroxanthoma: report of 8 lesions

PURPOSETo evaluate the suitability of treating atypical fibroxanthoma (AFX), an uncommon skin malignancy, with electronic brachytherapy. MATERIAL AND METHODSFrom Feb 2013 to Sep 2014, we were referred a total of 8 cases of AFX in 7 patients, all involving the scalp. All of them were treated with ele...

Full description

Saved in:
Bibliographic Details
Published inJournal of contemporary brachytherapy Vol. 9; no. 2; pp. 158 - 160
Main Authors Doggett, Stephen, Brazil, James, Limova, Marketa, Press, Leah, Smith, Sidney, Peck, Jeremy
Format Report
LanguageEnglish
Published 01.04.2017
Online AccessGet full text

Cover

Loading…
More Information
Summary:PURPOSETo evaluate the suitability of treating atypical fibroxanthoma (AFX), an uncommon skin malignancy, with electronic brachytherapy. MATERIAL AND METHODSFrom Feb 2013 to Sep 2014, we were referred a total of 8 cases of AFX in 7 patients, all involving the scalp. All of them were treated with electronic brachytherapy 50 Kev radiations (Xoft Axxent®, Fremont, California). All lesions received 40 Gy in two fractions per week with 5mm margins. RESULTSAt a median follow-up of 23.7 months, the local recurrence rate is 12.5%. The single lesion that failed was not debulked surgically prior to electronic brachytherapy. CONCLUSIONSTo our knowledge, this is the first report in the literature on the use of radiation therapy as curative primary treatment for AFX. No contraindication to the use of radiations is found in the literature, with surgery being the sole treatment for AFX noted. Our recurrence rate is 0% for debulked lesions. Risk of recurrence is mitigated with surgical debulking prior to brachytherapy. Electronic brachytherapy appears to be a safe and effective treatment for debulked AFX. Multiple excisions, skin grafting, and wound care can be avoided in elderly patients by the use of electronic brachytherapy.
Bibliography:ObjectType-Case Study-2
content type line 59
SourceType-Reports-1
ObjectType-Report-1
ISSN:1689-832X
DOI:10.5114/jcb.2017.65454