Pediatric extragonadal germ cell tumor of the scalp

被引:4
|
作者
Puri, A
Agarwala, S
Gupta, AK
Bhatnagar, V [1 ]
机构
[1] All India Inst Med Sci, Dept Pediat Surg, New Delhi 110029, India
[2] All India Inst Med Sci, Dept Radiodiag, New Delhi 110029, India
关键词
extragonadal germ cell tumor; scalp;
D O I
10.1053/jpsu.2001.27069
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Extragonadal germ cell tumors are relatively rare tumors, accounting for 5% to 10% of all germ cell tumors in adults. In children, approximately two thirds of germ cell tumors are extragonadal. Extragonadal germ cell tumor of the scalp is exceedingly rare. The authors report the case of a 1 1/2-year-old boy with extragonadal germ cell tumor over the occipital region. Examination of the chest, abdomen, and gonads was normal. Computed tomography scan of the head showed a large, well-defined, lobulated, heterogeneously enhancing soft tissue mass lesion in the occipital region. The underlying bone was normal with no evidence of intracranial extension. Biopsy results of the scalp mass showed features consistent with embroynal carcinoma. Serum alpha-fetoprotein (AFP) level was elevated. The child was started on chemotherapy and received 4 cycles of cisplatin, etoposide, and bleomycin (PEB). There was more than 90% reduction in the size of the mass at the end of the fourth cycle. The residual mass was excised and followed up with 2 cycles of postoperative FEB. Ten months after excision the patient is well, without recurrence, and the AFP level is normal. Copyright (C) 2001 by W.B. Saunders Company.
引用
收藏
页码:1602 / 1603
页数:2
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