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儿童内胚窦瘤

Endodermal sinus tumor in children.

作者信息

Davidoff A M, Hebra A, Bunin N, Shochat S J, Schnaufer L

机构信息

Department of Surgery, Children's Hospital of Philadelphia, PA 19104, USA.

出版信息

J Pediatr Surg. 1996 Aug;31(8):1075-8; discussion 1078-9. doi: 10.1016/s0022-3468(96)90090-1.

Abstract

Malignant germ cell tumors account for about 3% of neoplasms in children, and endodermal sinus tumor (EST) is the most common histological subtype. The authors reviewed 22 years' experience (at their institution) in the management of 37 patients with this tumor. Fifteen of them (41%) had a sacrococcygeal primary, 10 had a testicular tumor (27%), 6 had an ovarian tumor (16%), 3 had a vaginal tumor (8%) and 3 had tumors at other sites (8%). Seven (19%) patients presented with metastatic disease, primarily pulmonary. The serum alpha-fetoprotein (AFP) level was elevated in all cases tested. The initial chemotherapy regimen included vincristine, actinomycin, cyclophosphamide (VAC), and Adriamycin (6 patients), but since 1985 the regimen has been changed to include cisplatin or Carboplatin, etoposide, and bleomycin (21 patients). Eight patients with testicular tumors initially were treated with surgical excision alone. Computed tomography results were a poor predictor of recurrence, but AFP surveillance was extremely sensitive. No second-look operation detected residual tumor in the absence of AFP elevation. Initial relapse for all patients tended to occur early (within 2 years), locally, and often with pulmonary metastases. Although historically the prognosis for patients with EST has been poor, the overall 2-year survival rate in this series was 70%. The best prognosis was among the children who had a testicular primary tumor (survival rate, 100%). The 2-year survival rate for patients with ovarian tumors was 67%; for those with sacrococcygeal primaries it was 60%. These results suggest that the prognosis for children with EST has improved significantly over the past decade. Contributing factors include therapy based on cisplatin, etoposide, and bleomycin, and relapse surveillance with serial AFP determinations. Second-look procedures should be reserved for patients who have an increasing level of serum AFP, suspicious computed tomography findings, and no obvious evidence of metastatic disease.

摘要

恶性生殖细胞肿瘤约占儿童肿瘤的3%,而内胚窦瘤(EST)是最常见的组织学亚型。作者回顾了(其所在机构)22年来对37例该肿瘤患者的治疗经验。其中15例(41%)原发于骶尾部,10例为睾丸肿瘤(27%),6例为卵巢肿瘤(16%),3例为阴道肿瘤(8%),3例肿瘤位于其他部位(8%)。7例(19%)患者出现转移性疾病,主要为肺部转移。所有检测病例的血清甲胎蛋白(AFP)水平均升高。初始化疗方案包括长春新碱、放线菌素、环磷酰胺(VAC)和阿霉素(6例患者),但自1985年起,方案改为顺铂或卡铂、依托泊苷和博来霉素(21例患者)。8例睾丸肿瘤患者最初仅接受手术切除治疗。计算机断层扫描结果对复发的预测性较差,但AFP监测极为敏感。在AFP未升高的情况下,二次探查手术未发现残留肿瘤。所有患者的初始复发往往较早(2年内),多为局部复发,且常伴有肺部转移。尽管从历史上看,EST患者的预后较差,但本系列患者的总体2年生存率为70%。预后最佳的是原发性睾丸肿瘤患儿(生存率为100%)。卵巢肿瘤患者的2年生存率为67%;骶尾部原发性肿瘤患者的2年生存率为60%。这些结果表明,在过去十年中,EST患儿的预后有了显著改善。促成因素包括基于顺铂、依托泊苷和博来霉素的治疗,以及通过连续测定AFP进行复发监测。二次探查手术应仅用于血清AFP水平升高、计算机断层扫描结果可疑且无明显转移疾病证据的患者。

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