Hypothalamic hamartoma successfully treated by operation. Case report.
Hypothalamic hamartoma successfully treated by operation. Case report.
复制标题
下丘脑错构瘤通过手术成功治愈。
DOI：
10.3171/jns.1985.62.2.0288
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发表时间：
1985
影响因子：
4.1
通讯作者：
T. Kuwabara
中科院分区：
文献类型：
--
作者：
Y. Kyuma;E. Kato;K. Sekido;T. Kuwabara
一名18个月大的男孩被诊断出患有下丘脑错构瘤。当他1岁时，他出现了性早熟，在18个月大时，内分泌学检查显示卵泡刺激素、黄体生成素和睾酮水平异常高。错构瘤的中心被次全切除，正如术后计算机断层扫描所证实的那样。手术后性早熟消退。
An 18-month-old boy was diagnosed as having a hypothalamic hamartoma. When he was 1 year old, he developed precocious puberty, and at 18 months old, endocrinological tests revealed abnormally high follicle-stimulating hormone, luteinizing hormone, and testosterone levels. The center of the hamartoma was subtotally excised, as confirmed on the postoperative computerized tomography scan. Precocious puberty subsided after the operation.