Ostalo
Superficial Acral Fibromyxoma of the Great Toe: Case Report and Mini-Review of the Literature
Yusuke Wakabayashi
; Department of Dermatology, Kyoto Prefectural University of Medicine Graduate School of Medical Science 465 Kajii-cho, Kawaramachi Hirokoji, Kamigyo-ku Kyoto 602-8566 Japan
Noriaki Nakai
; Department of Dermatology, Kyoto Prefectural University of Medicine Graduate Sch
Hideya Takenaka
; Department of Dermatology, Kyoto Prefectural University of Medicine Graduate Sch
Norito Katoh
; Department of Dermatology, Kyoto Prefectural University of Medicine Graduate Sch
Sažetak
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.
Ključne riječi
superficial acral fibromyxoma; benign soft tissue tumor; mini-review; clinicopathologic characteristic
Hrčak ID:
95701
URI
Datum izdavanja:
11.1.2013.
Posjeta: 1.191 *