Case Ashley S, Kirby Tyler O, Conner Michael G, Huh Warner K
Department of Obstetrics and Gynecology, University of Alabama at Birmingham, 618 South 19th Street, Old Hillman Building, Room 340, Birmingham, AL 35233, USA.
Gynecol Oncol. 2005 Mar;96(3):850-3. doi: 10.1016/j.ygyno.2004.11.009.
Alveolar rhabdomyosarcoma is an uncommon malignant soft tissue tumor rarely found in the genital tract. This tumor is associated with a poor prognosis, especially in the adult population. Equally as rare are non-puerperal uterine inversions secondary to sarcomas.
A 21-year-old obese woman was initially evaluated with excessive vaginal bleeding. On exam, a large pedunculated mass protruding from the cervix was seen and biopsy of this mass revealed an alveolar rhabdomyosarcoma. The patient was treated with adjuvant chemotherapy consisting of VAC (Vincristine, Actinomycin, and Cyclophosphamide) for a presumed cervical rhabdomyosarcoma. After five cycles of chemotherapy the patient underwent a total abdominal hysterectomy and bilateral salpingo-oophorectomy, at which time a complete uterine inversion was noted with the tumor located at the fundus of the uterus. Final pathology showed alveolar rhabdomyosarcoma of the uterus. The patient then received additional postoperative VAC regimen for a total of 10 treatments and remains in good health with no evidence of disease 20 months from diagnosis.
This case report describes the only reported case of uterine inversion secondary to alveolar rhabdomyosarcoma of the uterus and discusses current therapeutic options for adults.
肺泡状横纹肌肉瘤是一种罕见的恶性软组织肿瘤,很少见于生殖道。该肿瘤预后较差,尤其是在成人中。同样罕见的是肉瘤继发的非产褥期子宫内翻。
一名21岁肥胖女性因阴道大量出血接受初步评估。检查时,可见一个从宫颈突出的带蒂大肿块,对该肿块进行活检显示为肺泡状横纹肌肉瘤。考虑到可能是宫颈横纹肌肉瘤,患者接受了由长春新碱、放线菌素和环磷酰胺组成的辅助化疗。化疗五个周期后,患者接受了全腹子宫切除术和双侧输卵管卵巢切除术,此时发现子宫完全内翻,肿瘤位于子宫底部。最终病理显示为子宫肺泡状横纹肌肉瘤。患者随后又接受了总共10次的术后VAC方案治疗,自诊断以来20个月一直健康,无疾病迹象。
本病例报告描述了唯一一例子宫肺泡状横纹肌肉瘤继发子宫内翻的病例,并讨论了成人目前的治疗选择。