{"title":"视神经胶质瘤对1型神经纤维瘤病青春期和生长的影响:来自三级中心的20年经验。","authors":"Robyn Haysom, Amish Chinoy","doi":"10.1177/08830738251341591","DOIUrl":null,"url":null,"abstract":"<p><p>Children with neurofibromatosis type 1 have an increased incidence of optic pathway gliomas and central precocious puberty. This study explores whether the presence and location of optic pathway gliomas is associated with the changes in height and pubertal onset that are seen in these children. Retrospective analysis was undertaken of 75 individuals with a diagnosis of both neurofibromatosis type 1 and optic pathway gliomas, known to a single quaternary neurofibromatosis type 1 center, over a 20-year period. Central precocious puberty was more likely with optic pathway gliomas, observed in 28% of the cohort, and was associated with either optic chiasm involvement (<i>P</i> = .046) or bilateral optic pathway gliomas (<i>P</i> < .001). This is presumably due to disruption in the hypothalamic-pituitary axis. Height standard deviation scores were not significantly different from the general population. Increased clinical monitoring of pubertal status is consequently required for children with neurofibromatosis type 1 and an optic pathway glioma.</p>","PeriodicalId":15319,"journal":{"name":"Journal of Child Neurology","volume":" ","pages":"8830738251341591"},"PeriodicalIF":2.0000,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Impact of Optic Pathway Gliomas on Puberty and Growth in Neurofibromatosis Type 1: A 20-Year Experience From a Tertiary Center.\",\"authors\":\"Robyn Haysom, Amish Chinoy\",\"doi\":\"10.1177/08830738251341591\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Children with neurofibromatosis type 1 have an increased incidence of optic pathway gliomas and central precocious puberty. This study explores whether the presence and location of optic pathway gliomas is associated with the changes in height and pubertal onset that are seen in these children. Retrospective analysis was undertaken of 75 individuals with a diagnosis of both neurofibromatosis type 1 and optic pathway gliomas, known to a single quaternary neurofibromatosis type 1 center, over a 20-year period. Central precocious puberty was more likely with optic pathway gliomas, observed in 28% of the cohort, and was associated with either optic chiasm involvement (<i>P</i> = .046) or bilateral optic pathway gliomas (<i>P</i> < .001). This is presumably due to disruption in the hypothalamic-pituitary axis. Height standard deviation scores were not significantly different from the general population. Increased clinical monitoring of pubertal status is consequently required for children with neurofibromatosis type 1 and an optic pathway glioma.</p>\",\"PeriodicalId\":15319,\"journal\":{\"name\":\"Journal of Child Neurology\",\"volume\":\" \",\"pages\":\"8830738251341591\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-05-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Child Neurology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1177/08830738251341591\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Child Neurology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/08830738251341591","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
Impact of Optic Pathway Gliomas on Puberty and Growth in Neurofibromatosis Type 1: A 20-Year Experience From a Tertiary Center.
Children with neurofibromatosis type 1 have an increased incidence of optic pathway gliomas and central precocious puberty. This study explores whether the presence and location of optic pathway gliomas is associated with the changes in height and pubertal onset that are seen in these children. Retrospective analysis was undertaken of 75 individuals with a diagnosis of both neurofibromatosis type 1 and optic pathway gliomas, known to a single quaternary neurofibromatosis type 1 center, over a 20-year period. Central precocious puberty was more likely with optic pathway gliomas, observed in 28% of the cohort, and was associated with either optic chiasm involvement (P = .046) or bilateral optic pathway gliomas (P < .001). This is presumably due to disruption in the hypothalamic-pituitary axis. Height standard deviation scores were not significantly different from the general population. Increased clinical monitoring of pubertal status is consequently required for children with neurofibromatosis type 1 and an optic pathway glioma.
期刊介绍:
The Journal of Child Neurology (JCN) embraces peer-reviewed clinical and investigative studies from a wide-variety of neuroscience disciplines. Focusing on the needs of neurologic patients from birth to age 18 years, JCN covers topics ranging from assessment of new and changing therapies and procedures; diagnosis, evaluation, and management of neurologic, neuropsychiatric, and neurodevelopmental disorders; and pathophysiology of central nervous system diseases.