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Permanent Central Diabetes Insipidus with Complete Regression of Pituitary Stalk Enlargement After 4 Years of Follow−up
A 14 year−old patient was admitted because of a history of polyuria and polydipsia. A diagnosis of central diabetes insipidus (CDI) accompanied by growth hormone (GH) and gonadotropin deficiency was made. Hypophyseal magnetic resonance imaging (MRI) of the patient demonstrated isolated pituitary sta...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Galenos Publishing
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005636/ https://www.ncbi.nlm.nih.gov/pubmed/21318063 http://dx.doi.org/10.4008/jcrpe.v1i1.4 |
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author | Öcal, Gönül Şıklar, Zeynep Berberoğlu, Merih Bilir, Pelin Engiz, Özlem Fitoz, Suat Arıcı, Serap |
author_facet | Öcal, Gönül Şıklar, Zeynep Berberoğlu, Merih Bilir, Pelin Engiz, Özlem Fitoz, Suat Arıcı, Serap |
author_sort | Öcal, Gönül |
collection | PubMed |
description | A 14 year−old patient was admitted because of a history of polyuria and polydipsia. A diagnosis of central diabetes insipidus (CDI) accompanied by growth hormone (GH) and gonadotropin deficiency was made. Hypophyseal magnetic resonance imaging (MRI) of the patient demonstrated isolated pituitary stalk enlargement. Although GH deficiency and gonadotropin deficiency were transient, CDI was persistent despite the regression of the pituitary stalk enlargement over the 4 years of follow−up. Conflict of interest:None declared. |
format | Text |
id | pubmed-3005636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Galenos Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-30056362011-01-27 Permanent Central Diabetes Insipidus with Complete Regression of Pituitary Stalk Enlargement After 4 Years of Follow−up Öcal, Gönül Şıklar, Zeynep Berberoğlu, Merih Bilir, Pelin Engiz, Özlem Fitoz, Suat Arıcı, Serap J Clin Res Pediatr Endocrinol Case Reports A 14 year−old patient was admitted because of a history of polyuria and polydipsia. A diagnosis of central diabetes insipidus (CDI) accompanied by growth hormone (GH) and gonadotropin deficiency was made. Hypophyseal magnetic resonance imaging (MRI) of the patient demonstrated isolated pituitary stalk enlargement. Although GH deficiency and gonadotropin deficiency were transient, CDI was persistent despite the regression of the pituitary stalk enlargement over the 4 years of follow−up. Conflict of interest:None declared. Galenos Publishing 2008-09 2008-08-06 /pmc/articles/PMC3005636/ /pubmed/21318063 http://dx.doi.org/10.4008/jcrpe.v1i1.4 Text en © Journal of Clinical Research in Pediatric Endocrinology, Published by Galenos Publishing. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Öcal, Gönül Şıklar, Zeynep Berberoğlu, Merih Bilir, Pelin Engiz, Özlem Fitoz, Suat Arıcı, Serap Permanent Central Diabetes Insipidus with Complete Regression of Pituitary Stalk Enlargement After 4 Years of Follow−up |
title | Permanent Central Diabetes Insipidus with Complete Regression of Pituitary Stalk Enlargement After 4 Years of Follow−up |
title_full | Permanent Central Diabetes Insipidus with Complete Regression of Pituitary Stalk Enlargement After 4 Years of Follow−up |
title_fullStr | Permanent Central Diabetes Insipidus with Complete Regression of Pituitary Stalk Enlargement After 4 Years of Follow−up |
title_full_unstemmed | Permanent Central Diabetes Insipidus with Complete Regression of Pituitary Stalk Enlargement After 4 Years of Follow−up |
title_short | Permanent Central Diabetes Insipidus with Complete Regression of Pituitary Stalk Enlargement After 4 Years of Follow−up |
title_sort | permanent central diabetes insipidus with complete regression of pituitary stalk enlargement after 4 years of follow−up |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005636/ https://www.ncbi.nlm.nih.gov/pubmed/21318063 http://dx.doi.org/10.4008/jcrpe.v1i1.4 |
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