首页> 外文期刊>Journal of cutaneous pathology >A case of cutaneous symplastic leiomyoma - a rare variant of cutaneous pilar leiomyoma.
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A case of cutaneous symplastic leiomyoma - a rare variant of cutaneous pilar leiomyoma.

机译:皮肤共生性平滑肌瘤一例-皮肤毛细血管平滑肌瘤的罕见变体。

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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.
机译:我们描述了一名37岁妇女皮肤共生性平滑肌瘤的病例,该病患者在左上臂出现缓慢缓慢的病灶已有4年历史。切除病灶并进行组织学检查。在由纺锤形细胞组成的真皮中发现了一个界限分明的病变,具有明显的核多态性。未见有丝分裂图或坏死。细胞被结蛋白和平滑肌肌动蛋白染色呈强阳性,而被S100,黑色素A,MNF116呈阴性的细胞角蛋白和CK5 / 6小鼠单克隆抗体呈阴性。认为该诊断与皮肤共生性平滑肌瘤一致,这是很少报道的柱状平滑肌瘤的变体。在组织学上,它显示出与子宫平滑肌瘤的共生变体相似的特征,具有细胞学上的异型性,核多态性和最小的有丝分裂活性。尽管长期前景可能是良性的,但任何纺锤状细胞肿瘤中细胞学上的异型性和有丝分裂的存在通常是一个令人关注的特征,需要长期随访。

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