Endocrine Disorder in Patients With Craniopharyngioma
Craniopharyngioma is an intracranial congenital epithelial tumor growing along the pathway of the embryonic craniopharyngeal tube. The main clinical symptoms of patients with craniopharyngioma include high intracranial pressure, visual field defect, endocrine dysfunction, and hypothalamic dysfunctio...
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Frontiers Media S.A.
2021
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oai:doaj.org-article:1ebfaddb50b34d729bae31bbdc625a8d2021-12-02T11:50:31ZEndocrine Disorder in Patients With Craniopharyngioma1664-229510.3389/fneur.2021.737743https://doaj.org/article/1ebfaddb50b34d729bae31bbdc625a8d2021-12-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fneur.2021.737743/fullhttps://doaj.org/toc/1664-2295Craniopharyngioma is an intracranial congenital epithelial tumor growing along the pathway of the embryonic craniopharyngeal tube. The main clinical symptoms of patients with craniopharyngioma include high intracranial pressure, visual field defect, endocrine dysfunction, and hypothalamic dysfunction. At present, the preferred treatment remains the surgical treatment, but the recovery of endocrine and hypothalamic function following surgery is limited. In addition, endocrine disorders often emerge following surgery, which seriously reduces the quality of life of patients after operation. So far, research on craniopharyngioma focuses on ways to ameliorate endocrine dysfunction. This article reviews the latest research progress on pathogenesis, manifestation, significance, and treatment of endocrine disorders in patients with craniopharyngioma.Zihao ZhouSheng ZhangFangqi HuFrontiers Media S.A.articlecraniopharyngiomaendocrine disorderspituitary hormone deficiencytreatmentriskNeurology. Diseases of the nervous systemRC346-429ENFrontiers in Neurology, Vol 12 (2021) |
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topic |
craniopharyngioma endocrine disorders pituitary hormone deficiency treatment risk Neurology. Diseases of the nervous system RC346-429 |
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craniopharyngioma endocrine disorders pituitary hormone deficiency treatment risk Neurology. Diseases of the nervous system RC346-429 Zihao Zhou Sheng Zhang Fangqi Hu Endocrine Disorder in Patients With Craniopharyngioma |
description |
Craniopharyngioma is an intracranial congenital epithelial tumor growing along the pathway of the embryonic craniopharyngeal tube. The main clinical symptoms of patients with craniopharyngioma include high intracranial pressure, visual field defect, endocrine dysfunction, and hypothalamic dysfunction. At present, the preferred treatment remains the surgical treatment, but the recovery of endocrine and hypothalamic function following surgery is limited. In addition, endocrine disorders often emerge following surgery, which seriously reduces the quality of life of patients after operation. So far, research on craniopharyngioma focuses on ways to ameliorate endocrine dysfunction. This article reviews the latest research progress on pathogenesis, manifestation, significance, and treatment of endocrine disorders in patients with craniopharyngioma. |
format |
article |
author |
Zihao Zhou Sheng Zhang Fangqi Hu |
author_facet |
Zihao Zhou Sheng Zhang Fangqi Hu |
author_sort |
Zihao Zhou |
title |
Endocrine Disorder in Patients With Craniopharyngioma |
title_short |
Endocrine Disorder in Patients With Craniopharyngioma |
title_full |
Endocrine Disorder in Patients With Craniopharyngioma |
title_fullStr |
Endocrine Disorder in Patients With Craniopharyngioma |
title_full_unstemmed |
Endocrine Disorder in Patients With Craniopharyngioma |
title_sort |
endocrine disorder in patients with craniopharyngioma |
publisher |
Frontiers Media S.A. |
publishDate |
2021 |
url |
https://doaj.org/article/1ebfaddb50b34d729bae31bbdc625a8d |
work_keys_str_mv |
AT zihaozhou endocrinedisorderinpatientswithcraniopharyngioma AT shengzhang endocrinedisorderinpatientswithcraniopharyngioma AT fangqihu endocrinedisorderinpatientswithcraniopharyngioma |
_version_ |
1718395151593766912 |