Grove A, Backman Nøhr S
Institute of Pathology, Aalborg Hospital, Denmark.
APMIS. 1992 Dec;100(12):1081-8. doi: 10.1111/j.1699-0463.1992.tb04044.x.
Superficial perineal leiomyosarcomas are rare, with only three previously reported examples. We encountered a superficial (deep subcutaneous) perineal leiomyosarcoma in a 17-year-old female. At follow-up two years after a wide excision, there were no signs of recurrence. The tumour was well differentiated and showed immunoreactivity for alpha-smooth muscle actin and desmin. A review of the literature on superficial leiomyosarcomas indicates that superficial perineal leiomyosarcomas may be more aggressive than superficial leiomyosarcomas in general. As the presented tumour occurred in a female, it was compared with vulvar leiomyosarcomas.
浅表会阴平滑肌肉瘤罕见,此前仅有3例报道。我们遇到1例17岁女性的浅表(深皮下)会阴平滑肌肉瘤。广泛切除术后两年随访,无复发迹象。肿瘤分化良好,对α-平滑肌肌动蛋白和结蛋白呈免疫反应性。对浅表平滑肌肉瘤的文献回顾表明,浅表会阴平滑肌肉瘤总体上可能比浅表平滑肌肉瘤更具侵袭性。由于该肿瘤发生在女性,故将其与外阴平滑肌肉瘤进行了比较。