Document Detail


Superficial acral fibromyxoma of the great toe: case report and mini-review of the literature.
MedLine Citation:
PMID:  23317489     Owner:  NLM     Status:  In-Data-Review    
Abstract/OtherAbstract:
Superficial acral fibromyxoma (SAF) is a rare, distinctive, benign soft tissue tumor with a predilection for the hands and feet, first described by Fetsch et al. in 2001. Histologically, SAF tumors are unencapsulated, mostly located in the dermis or subcutis, and composed of spindled and stellate-shaped cells with random, loose storiform and fascicular growth patterns. The stromal component of the tumor was Alcian blue-positive. The tumor cells were mostly immunopositive for CD34, vimentin, and CD99; often immunopositive for EMA; and immunonegative for S-100, HMB-45, SMA, desmin, and keratin. There have been 19 reports of 149 SAF cases in the English language literature. However, SAF is not widely recognized because it is an uncommon occurrence that has been described only relatively recently. Herein, we report a case of SAF and describe the clinicopathologic characteristics based on a review of published SAF cases from July 2001 to July 2011.
Authors:
Yusuke Wakabayashi; Noriaki Nakai; Hideya Takenaka; Norito Katoh
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Acta dermatovenerologica Croatica : ADC     Volume:  20     ISSN:  1847-6538     ISO Abbreviation:  Acta Dermatovenerol Croat     Publication Date:  2012 Dec 
Date Detail:
Created Date:  2013-01-15     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9433781     Medline TA:  Acta Dermatovenerol Croat     Country:  Croatia    
Other Details:
Languages:  eng     Pagination:  263-6     Citation Subset:  IM    
Affiliation:
Noriaki Nakai, MD, PhD, Department of Dermatology, Kyoto, Prefectural University of Medicine Graduate School of Medical Science, 465 Kajii-cho, Kawaramachi Hirokoji, Kamigyo-ku, Kyoto 602-8566, Japan; nnakai@koto.kpu-m.ac.jp.
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