Kim Ji Hyun, Kim Dong Chul, Lee Ryun, Shin Chi Ho, Han Yea Sik, Chung Sang Hun, Paik So Ya
Department of Plastic and Reconstructive Surgery, Bundang Jesaeng Hospital, Seongnam, Korea.
Department of Pathology, Bundang Jesaeng Hospital, Seongnam, Korea.
Arch Craniofac Surg. 2017 Dec;18(4):269-272. doi: 10.7181/acfs.2017.18.4.269. Epub 2017 Dec 23.
Myxoid solitary fibrous tumor (SFT) is very rare soft tissue neoplasm. It is microscopically composed of spindle cells which is individually separated by delicate band of collagen fibers. And this tumor cells are immunohisto-chemistrically highlighted by CD34. Myxoid SFT has indolent clinical course and a good prognosis, so it is important to make a diagnosis because of its morphological similarities to myxoid spindle cell neoplasms that have different prognoses and treatment. We report the case of a 20-year-old female with a myxoid SFT found in the left temporo-parietal scalp. This case report appears to be the first reported scalp occurrence of this rare tumor.
黏液样孤立性纤维性肿瘤(SFT)是一种非常罕见的软组织肿瘤。显微镜下,它由梭形细胞组成,这些细胞被纤细的胶原纤维带单个分隔开。并且这种肿瘤细胞在免疫组织化学上表现为CD34阳性。黏液样SFT临床病程惰性,预后良好,由于其形态与预后和治疗不同的黏液样梭形细胞瘤相似,因此做出诊断很重要。我们报告了一例20岁女性,其左侧颞顶头皮发现黏液样SFT。该病例报告似乎是首例报道的该罕见肿瘤发生于头皮的病例。