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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...

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Detalles Bibliográficos
Autores principales: Öcal, Gönül, Şıklar, Zeynep, Berberoğlu, Merih, Bilir, Pelin, Engiz, Özlem, Fitoz, Suat, Arıcı, Serap
Formato: Texto
Lenguaje:English
Publicado: Galenos Publishing 2008
Materias:
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.
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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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