Kaserer K, Kainz C, Reinthaller A, Amann G, Beer F, Breitenecker G
Gynäkopathologische Abteilung, Institut für klinische Pathologie, Universität Wien, Allgemeines Krankenhaus.
Pathologe. 1995 Jul;16(4):287-91. doi: 10.1007/s002920050104.
Embryonal rhabdomyosarcomas of the female genital tract usually occur during infancy in the vagina. Only in rare cases can they be found in the cervix, where they are most commonly seen in adolescence. Their prognosis seems to be good since the introduction of a combination of surgery and chemotherapy. We report a case of cervical embryonal rhabdomysarcoma in IRS stage Ia in a 32-year-old female. After surgical resection and chemotherapy there has been no evidence of disease for 7 months. The case is compared with the published literature and prognostically relevant features, and possible problems in the differential diagnosis in biopsies are discussed.
女性生殖道胚胎性横纹肌肉瘤通常发生于婴儿期的阴道。仅在极少数情况下可出现在宫颈,多见于青春期。自采用手术和化疗联合治疗以来,其预后似乎良好。我们报告一例32岁女性处于国际横纹肌肉瘤分期(IRS)Ia期的宫颈胚胎性横纹肌肉瘤病例。手术切除及化疗后7个月无疾病证据。将该病例与已发表文献及预后相关特征进行比较,并讨论活检中鉴别诊断可能存在的问题。