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

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 uncomm...

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Detalles Bibliográficos
Autores principales: Kasim, Nader, Choudhri, Asim, Alemzadeh, Ramin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007484/
https://www.ncbi.nlm.nih.gov/pubmed/29977576
http://dx.doi.org/10.1093/omcr/omy018
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author Kasim, Nader
Choudhri, Asim
Alemzadeh, Ramin
author_facet Kasim, Nader
Choudhri, Asim
Alemzadeh, Ramin
author_sort Kasim, Nader
collection PubMed
description 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.
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spelling pubmed-60074842018-07-05 Craniopharyngeal canal, morning glory disc anomaly and hypopituitarism: what do they have in common? Kasim, Nader Choudhri, Asim Alemzadeh, Ramin Oxf Med Case Reports Case Report 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. Oxford University Press 2018-06-11 /pmc/articles/PMC6007484/ /pubmed/29977576 http://dx.doi.org/10.1093/omcr/omy018 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Kasim, Nader
Choudhri, Asim
Alemzadeh, Ramin
Craniopharyngeal canal, morning glory disc anomaly and hypopituitarism: what do they have in common?
title Craniopharyngeal canal, morning glory disc anomaly and hypopituitarism: what do they have in common?
title_full Craniopharyngeal canal, morning glory disc anomaly and hypopituitarism: what do they have in common?
title_fullStr Craniopharyngeal canal, morning glory disc anomaly and hypopituitarism: what do they have in common?
title_full_unstemmed Craniopharyngeal canal, morning glory disc anomaly and hypopituitarism: what do they have in common?
title_short Craniopharyngeal canal, morning glory disc anomaly and hypopituitarism: what do they have in common?
title_sort craniopharyngeal canal, morning glory disc anomaly and hypopituitarism: what do they have in common?
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007484/
https://www.ncbi.nlm.nih.gov/pubmed/29977576
http://dx.doi.org/10.1093/omcr/omy018
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