Successful multimodality therapy of recurrent multifocal juvenile granulosa cell tumor of the ovary

被引：18

作者：

Erdreich-Epstein, A

Monforte, HL

Lavey, RS

Joshi, S

Phillips, JD

Villablanca, JG

机构：

[1] Childrens Hosp Los Angeles, Div Hematol Oncol, Keck Sch Med, Dept Pediat, Los Angeles, CA 90027 USA

[2] Childrens Hosp Los Angeles, Dept Pathol, Keck Sch Med, Los Angeles, CA 90027 USA

[3] Childrens Hosp Los Angeles, Dept Radiat Oncol, Keck Sch Med, Los Angeles, CA 90027 USA

[4] Univ So Calif, Los Angeles, CA USA

[5] Univ N Carolina, Dept Surg, Sch Med, Chapel Hill, NC USA

来源：

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY | 2002年 / 24卷 / 03期

关键词：

autologous bone marrow transplant; chemotherapy; juvenile granulosa cell tumor; radiation;

D O I：

10.1097/00043426-200203000-00015

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Juvenile granulosa cell tumor (JGCT) of the ovary, a rare pediatric cancer, carries a very poor prognosis in advanced and recurrent cases. A 10-year-old girl with stage IA JGCT, initially treated with resection only, presented with extensive unresectable multifocal pelvic recurrence. She underwent surgery, chemotherapy (cisplatin/paclitaxel alternating with cisplatin/cyclophosphamide/etoposide/bleomycin), myeloablative chemotherapy (carboplatin/etoposide/melphalan) with autologous bone marrow transplant, and pelvic radiation. She tolerated therapy well and is in complete remission 69 months after her recurrence.

引用

页码：229 / 233

页数：5

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