Suppr超能文献

髓母细胞瘤患儿手术后、放疗和化疗后的长期内分泌后遗症。

Long-term endocrine sequelae after surgery, radiotherapy, and chemotherapy in children with medulloblastoma.

作者信息

Pasqualini T, Diez B, Domene H, Escobar M E, Gruñeiro L, Heinrich J J, Martinez A, Iorcansky S, Sackmann-Muriel F, Rivarola M

出版信息

Cancer. 1987 Feb 15;59(4):801-6. doi: 10.1002/1097-0142(19870215)59:4<801::aid-cncr2820590424>3.0.co;2-z.

Abstract

Thirteen children with medulloblastoma, were studied after 2 to 62 months off radiotherapy and chemotherapy with methotrexate and BCNU. Ages at time of study ranged from 2.3 to 15.7 years. Eleven patients, followed for a mean of 22 months, showed a significant decrease of height score, whereas nine patients had deficient growth hormone (GH) response to provocative tests. Clinical pubertal progression was normal in all patients, and three of five girls with advanced pubertal development had menarche. No evidences of gonadotropin disturbances were found in five patients whereas seven had raised basal follicle-stimulating hormone (FSH) level or FSH response to luteinizing hormone-releasing hormone (LH-RH). Abnormalities in thyrotrophin (TSH) secretion were found in 9 of 13 patients. This study shows that poor growth and GH deficiency were frequent in our patients. The high frequency of thyroid disturbances observed point out the need of evaluating thyroid function for adequate replacement therapy. Perhaps modification of adjuvant chemotherapy in the future can diminish drug-induced gonadal damage.

摘要

对13名髓母细胞瘤患儿在停止放疗以及使用甲氨蝶呤和卡氮芥进行化疗2至62个月后进行了研究。研究时患儿年龄在2.3岁至15.7岁之间。11名平均随访22个月的患者身高评分显著下降,而9名患者对激发试验的生长激素(GH)反应不足。所有患者的临床青春期发育进程均正常,5名青春期发育提前的女孩中有3名月经初潮。5名患者未发现促性腺激素紊乱的证据,而7名患者基础促卵泡生成素(FSH)水平升高或FSH对促黄体生成素释放激素(LH-RH)的反应增强。13名患者中有9名促甲状腺激素(TSH)分泌异常。这项研究表明,生长发育不良和生长激素缺乏在我们的患者中很常见。观察到的甲状腺功能紊乱的高频率表明需要评估甲状腺功能以进行适当的替代治疗。也许未来辅助化疗方案的调整可以减少药物引起的性腺损伤。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验