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下丘脑错构瘤与性早熟:一例报告

Hypothalamic hamartoma and precocious puberty: report of a case.

作者信息

Hsiao P H, Tsai W Y, Lee J S, Liu H M, Hsieh F J

机构信息

Department of Pediatrics, National Taiwan University Hospital, Taipei, R.O.C.

出版信息

J Formos Med Assoc. 1992 Oct;91(10):1017-20.

PMID:1362668
Abstract

Hypothalamic hamartoma is reported to be associated with precocious puberty. Here, the authors present a seven-year-old girl whose onset of puberty occurred at the age of two. Under the impression of idiopathic precocious puberty, cyproterone acetate was initially tried. Since the effect of her medication was not satisfactory, it was discontinued at the age of five years and 11 months. However, rapid advance of bone age and vaginal spotting recurred after the withdrawal of treatment. She was re-evaluated at the age of six, and a magnetic resonance image (MRI) study of the head revealed a hypothalamic hamartoma. At that time, a long-acting analog of luteinizing hormone-releasing hormone (LHRHa), leuprolide acetate, was prescribed. Her secondary sex characteristics regressed and her hypothalamic-pituitary-gonad axis was suppressed after treatment. The clinical presentation, mechanism and treatment of precocious puberty caused by hypothalamic hamartomas are fully discussed in this report.

摘要

据报道,下丘脑错构瘤与性早熟有关。在此,作者介绍了一名七岁女孩,其在两岁时开始出现青春期发育。在特发性性早熟的诊断印象下,最初尝试使用醋酸环丙孕酮。由于药物治疗效果不佳,在五岁零十一个月时停药。然而,停药后骨龄迅速增长且再次出现阴道点滴出血。她在六岁时接受了重新评估,头部磁共振成像(MRI)检查发现了下丘脑错构瘤。当时,开具了长效促黄体生成素释放激素(LHRHa)类似物醋酸亮丙瑞林。治疗后,她的第二性征消退,下丘脑 - 垂体 - 性腺轴受到抑制。本报告全面讨论了下丘脑错构瘤所致性早熟的临床表现、机制及治疗。

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