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颅咽管、牵牛花盘状异常与垂体功能减退:它们有何共同之处?

Craniopharyngeal canal, morning glory disc anomaly and hypopituitarism: what do they have in common?

作者信息

Kasim Nader, Choudhri Asim, Alemzadeh Ramin

机构信息

Le Bonheur Children's Hospital, Memphis, TN, USA.

Department of Pediatric Endocrinology, University of Tennessee Health Science Center, Memphis, TN, USA.

出版信息

Oxf Med Case Reports. 2018 Jun 11;2018(6):omy018. doi: 10.1093/omcr/omy018. eCollection 2018 Jun.

DOI:10.1093/omcr/omy018
PMID:29977576
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6007484/
Abstract

A 14-year-old girl with a history of mid-line defects, basal encephalocele and morning glory disc anomaly presented with untreated growth hormone deficiency, pubertal delay and hypothyroidism. She was found to have a large craniopharyngeal canal based on MRI scan. Craniopharyngeal canal is an uncommon condition that has not been well described in the pediatric population. Consideration of craniopharyngeal canal in the differential diagnosis for basal encephaloceles and understanding its presentation can impact medical decision making and follow-up for patients.

摘要

一名14岁女孩,有中线缺陷、基底脑膨出和牵牛花盘状异常病史,出现未经治疗的生长激素缺乏、青春期延迟和甲状腺功能减退。根据磁共振成像扫描,发现她有一个大的颅咽管。颅咽管是一种罕见的疾病,在儿科人群中尚未得到充分描述。在基底脑膨出的鉴别诊断中考虑颅咽管并了解其表现,会影响患者的医疗决策和随访。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cf4/6007484/90a96e5c2c16/omy018f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cf4/6007484/90a96e5c2c16/omy018f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cf4/6007484/90a96e5c2c16/omy018f01.jpg

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Persisting Embryonal Infundibular Recess in Morning Glory Syndrome: Clinical Report of a Novel Association.永存胚胎漏斗部凹陷在牵牛花综合征中的新关联:临床报告。

本文引用的文献

1
Craniopharyngeal canal and its spectrum of pathology.颅咽管及其病变谱。
AJNR Am J Neuroradiol. 2014 Apr;35(4):772-7. doi: 10.3174/ajnr.A3745. Epub 2013 Nov 1.
2
Morning glory disc anomaly: characteristic MR imaging findings.朝颜盘畸形:特征性磁共振成像表现。
AJNR Am J Neuroradiol. 2013 Oct;34(10):2010-4. doi: 10.3174/ajnr.A3542. Epub 2013 May 9.
3
Rathke's pouch remnant and its regression process in the prenatal period.拉特克囊残余物及其在胎儿期的退化过程。
AJNR Am J Neuroradiol. 2019 May;40(5):899-902. doi: 10.3174/ajnr.A6005. Epub 2019 Mar 7.
4
Prevalence of anatomical variants in the clivus: fossa navicularis magna, canalis basilaris medianus, and craniopharyngeal canal.斜坡解剖变异的患病率:大舟状窝、基底正中管和颅咽管。
Surg Radiol Anat. 2019 Apr;41(4):477-483. doi: 10.1007/s00276-019-02200-3. Epub 2019 Feb 6.
Childs Nerv Syst. 2013 May;29(5):761-9. doi: 10.1007/s00381-012-2015-2. Epub 2013 Jan 12.
4
The Craniopharyngeal Canal in Man and Anthropoids.人类和类人猿的颅咽管。
J Anat. 1931 Apr;65(Pt 3):363-7.
5
The craniopharyngeal canal reviewed and reinterpreted.颅咽管的回顾与重新诠释。
Anat Rec. 1950 Jan;106(1):1-16. doi: 10.1002/ar.1091060102.
6
Encephaloceles of the anterior cranial fossa.前颅窝脑膨出
Pediatr Neurosurg. 1995;23(3):148-58. doi: 10.1159/000120952.
7
Human fetal pituitary gland in holoprosencephaly and anencephaly.全前脑畸形和无脑儿中的人类胎儿垂体
J Craniofac Genet Dev Biol. 1995 Oct-Dec;15(4):222-9.
8
Basal encephaloceles with morning glory syndrome, and progressive hormonal and visual disturbances: case report and review of the literature.
Brain Dev. 1995 May-Jun;17(3):196-201. doi: 10.1016/0387-7604(95)00021-3.
9
Transsphenoidal encephaloceles.
Surg Neurol. 1983 Dec;20(6):471-80. doi: 10.1016/0090-3019(83)90030-7.
10
Anterior basal encephalocele of the neonatal and infantile period.新生儿和婴儿期前基底型脑膨出
Neurosurgery. 1986 Sep;19(3):468-78. doi: 10.1227/00006123-198609000-00025.