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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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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. |
format | Online Article Text |
id | pubmed-6007484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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