Hachi H, Ottmany A, Bougtab A, Achaachi L, Baroudi C E, Tijami F, Jalil A, Benjelloune S, Ahyoud F, Souadka A, al Bouzidi A, Gamra L, Belabas M, Benomar S
Institut national d'oncologie Sidi Mohammed Ben Abdellah, Rabat, Maroc.
Bull Cancer. 1997 Feb;84(2):215-7.
Vaginal leiomyosarcoma is unfrequent. We report on a case in a 50-year-old multipara patient who had presented a posterior vaginal swelling since 6 months. The tumor was discovered at the occasion of pains and non hemorragic discharge. The histological pattern of the tumor was well-differentiated spindle cell sarcoma with pleiomorphic areas. The immunohistochemistry confirmed the smooth myogenic differentiation. The treatment consisted of posterior pelvic exenteration extended to the vagina. The patient is alive and free of disease at 20 months of fellow-up.
阴道平滑肌肉瘤并不常见。我们报告一例50岁经产妇病例,该患者6个月来一直存在阴道后壁肿物。肿瘤是在出现疼痛和非血性分泌物时被发现的。肿瘤的组织学类型为高分化梭形细胞肉瘤,伴有多形性区域。免疫组化证实为平滑肌源性分化。治疗包括扩大至阴道的后盆腔脏器清除术。随访20个月时患者存活且无疾病复发。