Kazadi Buanga J, De Alava Casado E, Jurado Chacon M
Departamento de Ginecologia, Clinica Universitaria, Pamplona, Navarra, Espana.
Rev Fr Gynecol Obstet. 1995 Apr-May;90(4):222-7.
Vaginal leiomyosarcoma is a very rare tumor. The authors report a case of primary presentation in a 51-year-old multipara who complained of the development, since about 12 months previously, of a vaginal swelling accompanied by bloody discharge and pain. The outcome was fatal twenty two months later following treatment combining chemotherapy, radiotherapy, and surgery. The case is discussed in the light of data from the literature.
阴道平滑肌肉瘤是一种非常罕见的肿瘤。作者报告了一例51岁经产妇的原发性病例,该患者自大约12个月前开始出现阴道肿物,并伴有血性分泌物和疼痛。在联合化疗、放疗和手术治疗22个月后,患者死亡。本文结合文献数据对该病例进行了讨论。