Usmani Naila, Merchant W, Yung A
Department of Dermatology, Leeds General Infirmary, Leeds, UK.
J Cutan Pathol. 2008 Mar;35(3):329-31. doi: 10.1111/j.1600-0560.2007.00803.x.
We describe the case of a cutaneous symplastic leiomyoma in a 37-year-old woman who presented with a 4-year history of a painful slow growing lesion on the left upper arm. The lesion was excised and subjected to histological examination. A poorly circumscribed lesion was seen in the dermis composed of spindle shaped cells with marked nuclear pleomorphism. No mitotic figures or necrosis were seen. The cells stained strongly positive with desmin and smooth muscle actin, and negative with S100, melan A, MNF116 a mouse monoclonal antibody to cytokeratin and CK5/6. The diagnosis was felt to be in keeping with a cutaneous symplastic leiomyoma, a rarely reported variant of the pilar leiomyoma. Histologically, it shows features similar to the symplastic variant of uterine leiomyoma with cytological atypia, nuclear pleomorphism and minimal mitotic activity. Although the long-term outlook is probably benign, the presence of cytological atypia and mitoses in any spindle cell tumor is generally a concerning feature and warrants long-term follow up.
我们描述了一名37岁女性皮肤异型性平滑肌瘤的病例,该患者左上臂出现一个疼痛性缓慢生长的肿物,病史长达4年。肿物被切除并进行组织学检查。真皮层可见一个边界不清的肿物,由梭形细胞组成,细胞核具有明显的多形性。未见核分裂象或坏死。细胞结蛋白和平滑肌肌动蛋白染色呈强阳性,而S100、黑素A、MNF116(一种抗细胞角蛋白的小鼠单克隆抗体)和CK5/6染色呈阴性。诊断为皮肤异型性平滑肌瘤,这是一种很少报道的毛囊平滑肌瘤变体。组织学上,它表现出与子宫平滑肌瘤异型性变体相似的特征,具有细胞学异型性、核多形性和最小限度的核分裂活性。虽然长期预后可能是良性的,但任何梭形细胞瘤中出现细胞学异型性和核分裂象通常都是令人担忧的特征,需要长期随访。