Kurtoglu E, Celik H, Kokcu A, Kefeli M, Ozdemir A Z, Danaci M
Eur J Gynaecol Oncol. 2016;37(3):401-3.
Primary sarcomas account for of 2-3% of all female genital tract cancers and ovaries are unusual sites for sarcomas. The authors aimed to report a case of primary ovarian sarcoma.
A 46-year-old woman presented with abdominal pain and distention. Abdominal MRI revealed a 20-cm-sized complex mass in the right adnexa and ascites. Preoperative CA-125 was 289 U/ml. She underwent optimal debulking surgery and diagnosed with undifferentiated pleomorphic sarcoma with focally rhabdomyosarcomatous differentiation.
The patient presented with severe abdominal pain and distention 32 days after the operation and recurrent disease was diagnosed. First cure of adjuvant chemotherapy was administered, but she died 15 days later.
Coexistence of undifferentiated pleomorphic sarcoma and rhabdomyosarcoma shows highly aggressive behavior and its prognosis is extremely poor. To the best of the authors' knowledge, this is the second case report of the coexistence of these type tumors in the literature.
原发性肉瘤占所有女性生殖道癌症的2 - 3%,卵巢是肉瘤的罕见发病部位。作者旨在报告一例原发性卵巢肉瘤病例。
一名46岁女性因腹痛和腹胀就诊。腹部磁共振成像(MRI)显示右附件区有一个20厘米大小的复杂肿块及腹水。术前癌抗原125(CA - 125)为289 U/ml。她接受了肿瘤细胞减灭术,术后诊断为伴有局灶性横纹肌肉瘤分化的未分化多形性肉瘤。
患者术后32天出现严重腹痛和腹胀,诊断为疾病复发。首先给予辅助化疗,但她在15天后死亡。
未分化多形性肉瘤和横纹肌肉瘤并存表现出高度侵袭性,其预后极差。据作者所知,这是文献中第二例关于这两种类型肿瘤并存的病例报告。