Goo Jawoong, Jung Ye-Jin, Kim Jae-Hong, Lee Sung-Yul, Ahn Sung Ku
Department of Dermatology, Wonju College of Medicine, Yonsei University, Wonju, Korea.
Ann Dermatol. 2010 Feb;22(1):110-3. doi: 10.5021/ad.2010.22.1.110. Epub 2010 Feb 28.
Superficial acral fibromyxoma (SAFM) is a rare myxoid tumor that was first described in 2001. The presence of a very slow growing solitary tender mass in the subungual area is the typical clinical feature at presentation. Histopathologically, SAFM is composed of stellate cells in a myxocollagenous matrix with a poorly circumscribed margin. This tumor is thought to be benign, but its natural course is not fully understood. We describe a 15-year-old patient with recurrent SAFM and discuss the proper treatment and follow up.
浅表性肢端纤维黏液瘤(SAFM)是一种罕见的黏液样肿瘤,于2001年首次被描述。甲下区域出现生长极为缓慢的孤立性压痛肿块是其典型的临床表现。组织病理学上,SAFM由位于黏液胶原基质中的星状细胞组成,边界不清。该肿瘤被认为是良性的,但其自然病程尚未完全明确。我们报道一名15岁复发性SAFM患者,并讨论恰当的治疗及随访措施。