Mandai K, Moriwaki S, Motoi M
Division of Pathology, Shikoku Cancer Center Hospital, Matsuyama, Japan.
Acta Pathol Jpn. 1990 Dec;40(12):927-34. doi: 10.1111/j.1440-1827.1990.tb03340.x.
A case of aggressive angiomyxoma of the vulva is reported. A 43-year-old woman presented initially in 1987 with a left vulvar mass which clinically was thought to be a lipoma or a Bartholin gland cyst. Local excision was performed after a 27-month follow-up without any change in size. The resected tumor measured 2.7 x 2.0 x 2.0 cm and had a smooth, glistening and myxoid cut surface. Histologically, the lesion was composed of spindle-shaped or stellate neoplastic cells, which were loosely textured in the fibromyxoid matrix, and a prominent vascular component characterized by randomly distributed vascular channels of variable caliber. Immunohistochemically, the tumor cells were positive for vimentin, but not for desmin and myosin. The fine structure of the neoplastic cells was compatible with that of fibroblasts rather than myofibroblasts. These findings suggest the fibroblastic differentiation of this tumor. The patient is currently well with no evidence of recurrence, 7 months after excision of the tumor.
本文报告了一例外阴侵袭性血管黏液瘤。一名43岁女性于1987年初因左侧外阴肿物就诊,临床考虑为脂肪瘤或巴氏腺囊肿。经过27个月的随访,肿物大小无变化,遂行局部切除术。切除的肿瘤大小为2.7×2.0×2.0 cm,切面光滑、发亮,呈黏液样。组织学上,病变由梭形或星状肿瘤细胞组成,这些细胞在纤维黏液样基质中排列疏松,并有一个显著的血管成分,其特征为口径不一的血管通道随机分布。免疫组化显示,肿瘤细胞波形蛋白阳性,结蛋白和肌球蛋白阴性。肿瘤细胞的超微结构与成纤维细胞而非肌成纤维细胞相符。这些发现提示该肿瘤具有成纤维细胞分化。肿瘤切除7个月后,患者目前情况良好,无复发迹象。