中国肿瘤临床
中國腫瘤臨床
중국종류림상
CHINESE JOURNAL OF CLINICAL ONCOLOGY
2014年
9期
589-592
,共4页
李林%吴令英%张蓉%宋艳%李晓光%马绍康%白萍
李林%吳令英%張蓉%宋豔%李曉光%馬紹康%白萍
리림%오령영%장용%송염%리효광%마소강%백평
卵巢肿瘤%小细胞癌%治疗%预后
卵巢腫瘤%小細胞癌%治療%預後
란소종류%소세포암%치료%예후
ovarian neoplasm%small cell carcinoma%treatment%prognosis
目的:探讨原发性卵巢小细胞癌(Small Cell Carcinoma of the Ovary,SCCO)临床病理特点、诊断、治疗及预后。方法:对中国医学科学院肿瘤医院2005年1月至2012年12月收治的4例SCCO病例资料进行回顾性分析。结果:4例SCCO患者平均发病年龄43.75(17~57)岁;绝经后2例,<30岁l例。Ⅰ期1例,Ⅲ~Ⅳ期3例。除1例无法分型外,余3例均为肺型。4例患者中1例行保留生育功能手术,3例行减瘤术;4例患者术后均给予铂类为基础的多药联合化疗,3例行TC方案化疗,无术后放疗者。本组治疗后随诊7~30个月,2例于初次诊断后的9、12个月死于本病,2例治疗后分别生存7、30个月,无复发迹象。结论:SCCO较罕见,预后差,免疫组织化学检测可用于鉴别诊断。治疗上以减瘤术及术后铂类为基础化疗为主要手段,最优化疗方案仍需进一步研究。
目的:探討原髮性卵巢小細胞癌(Small Cell Carcinoma of the Ovary,SCCO)臨床病理特點、診斷、治療及預後。方法:對中國醫學科學院腫瘤醫院2005年1月至2012年12月收治的4例SCCO病例資料進行迴顧性分析。結果:4例SCCO患者平均髮病年齡43.75(17~57)歲;絕經後2例,<30歲l例。Ⅰ期1例,Ⅲ~Ⅳ期3例。除1例無法分型外,餘3例均為肺型。4例患者中1例行保留生育功能手術,3例行減瘤術;4例患者術後均給予鉑類為基礎的多藥聯閤化療,3例行TC方案化療,無術後放療者。本組治療後隨診7~30箇月,2例于初次診斷後的9、12箇月死于本病,2例治療後分彆生存7、30箇月,無複髮跡象。結論:SCCO較罕見,預後差,免疫組織化學檢測可用于鑒彆診斷。治療上以減瘤術及術後鉑類為基礎化療為主要手段,最優化療方案仍需進一步研究。
목적:탐토원발성란소소세포암(Small Cell Carcinoma of the Ovary,SCCO)림상병리특점、진단、치료급예후。방법:대중국의학과학원종류의원2005년1월지2012년12월수치적4례SCCO병례자료진행회고성분석。결과:4례SCCO환자평균발병년령43.75(17~57)세;절경후2례,<30세l례。Ⅰ기1례,Ⅲ~Ⅳ기3례。제1례무법분형외,여3례균위폐형。4례환자중1례행보류생육공능수술,3례행감류술;4례환자술후균급여박류위기출적다약연합화료,3례행TC방안화료,무술후방료자。본조치료후수진7~30개월,2례우초차진단후적9、12개월사우본병,2례치료후분별생존7、30개월,무복발적상。결론:SCCO교한견,예후차,면역조직화학검측가용우감별진단。치료상이감류술급술후박류위기출화료위주요수단,최우화료방안잉수진일보연구。
Objective:This study analyzes the clinicopathological characteristics, pathological diagnosis, treatment, and prognosis of ovarian small cell carcinoma (SCCO). Methods:The medical records of SCCO patients in the Cancer Hospital of Peking Union Medical College between 2005 and 2012 were reviewed. Results:The mean age of patients was 43. 75 years old (ranging from 17 to 57), two cases were postmenopausal, and one case was less than 30 years old. Twenty-one patients had FIGO stageⅠ, whereas three cases had stageⅢto Ⅳ. Three cases were classified as pulmonary type. Forty-three patients received cytoreductive surgery, and one underwent fertili ty-conserving surgery. All patients were postoperatively treated with platinum-based chemotherapy, whereas three cases received Paclitaxel plus Carboplatin. No patient received adjuvant radiotherapy. One patient died nine months after the initial diagnosis, and one died 12 months after the initial diagnosis. The other two cases remain alive with no evidence of recurrence after follow up at 7 and 30 months after diagnosis. Conclusion:SCCO is a rare ovarian tumor with high malignancy potential and thus has poor prognosis. The clinical manifestations of SCCO resemble those of epithelial ovarian cancer. Immunohistochemistry can be used for differential diagnosis. The standard SCCO treatments are cytoreductive surgery and adjuvant platinum-based chemotherapy. The optimal chemotherapy regimen requires further research.