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Congenital Adrenal Hyperplasia and Brain Magnetic Resonance Imaging Abnormalities

A 15-yr-old male patient with congenital adrenal hyperplasia (CAH) was referred to our department with a one year history of gradual worsening of tremors. He was diagnosed with salt-wasting 21-hydroxylase deficiency CAH at 40 d old and was started on hydrocortisone, fludrocortisone and salt. He was...

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Autores principales: Samia, Younes-Mhenni, Mahdi, Kamoun, Baha, Zantour, Saida, Jerbi-Ommezine, Tahar, Sfar Mohamed, Habib, Sfar Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687627/
https://www.ncbi.nlm.nih.gov/pubmed/23926386
http://dx.doi.org/10.1297/cpe.19.109
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author Samia, Younes-Mhenni
Mahdi, Kamoun
Baha, Zantour
Saida, Jerbi-Ommezine
Tahar, Sfar Mohamed
Habib, Sfar Mohamed
author_facet Samia, Younes-Mhenni
Mahdi, Kamoun
Baha, Zantour
Saida, Jerbi-Ommezine
Tahar, Sfar Mohamed
Habib, Sfar Mohamed
author_sort Samia, Younes-Mhenni
collection PubMed
description A 15-yr-old male patient with congenital adrenal hyperplasia (CAH) was referred to our department with a one year history of gradual worsening of tremors. He was diagnosed with salt-wasting 21-hydroxylase deficiency CAH at 40 d old and was started on hydrocortisone, fludrocortisone and salt. He was found to have hypertension at 8 yr of age. Detailed investigations failed to detect any cause for secondary hypertension. Physical findings on the current hospitalization objectified obesity, blood pressure of 150/80 mmHg, postural and action tremor, left cerebellar syndrome, reflex tetra pyramidal syndrome and mental decline. Brain magnetic resonance imaging (MRI) showed bilateral periventricular white matter hyperintensity that was more pronounced in the posterior regions and associated with cortico-subcortical atrophy and complete agenesis of the corpus callosum. All investigations for leukoencephalopathy were negative. A diagnosis of brain MRI abnormalities related to CAH was made, and the patient received symptomatic treatment of tremors. Our case report provides evidence of an increased frequency of brain MRI abnormalities in CAH. The literature suggests hormonal imbalance and exposure to excess exogenous glucocorticoids as main probable mechanisms. Thus, in clinical practice, CAH should be considered as one of the possible causes of brain white matter involvement associated with or without cerebral atrophy.
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spelling pubmed-36876272013-08-07 Congenital Adrenal Hyperplasia and Brain Magnetic Resonance Imaging Abnormalities Samia, Younes-Mhenni Mahdi, Kamoun Baha, Zantour Saida, Jerbi-Ommezine Tahar, Sfar Mohamed Habib, Sfar Mohamed Clin Pediatr Endocrinol Case Report A 15-yr-old male patient with congenital adrenal hyperplasia (CAH) was referred to our department with a one year history of gradual worsening of tremors. He was diagnosed with salt-wasting 21-hydroxylase deficiency CAH at 40 d old and was started on hydrocortisone, fludrocortisone and salt. He was found to have hypertension at 8 yr of age. Detailed investigations failed to detect any cause for secondary hypertension. Physical findings on the current hospitalization objectified obesity, blood pressure of 150/80 mmHg, postural and action tremor, left cerebellar syndrome, reflex tetra pyramidal syndrome and mental decline. Brain magnetic resonance imaging (MRI) showed bilateral periventricular white matter hyperintensity that was more pronounced in the posterior regions and associated with cortico-subcortical atrophy and complete agenesis of the corpus callosum. All investigations for leukoencephalopathy were negative. A diagnosis of brain MRI abnormalities related to CAH was made, and the patient received symptomatic treatment of tremors. Our case report provides evidence of an increased frequency of brain MRI abnormalities in CAH. The literature suggests hormonal imbalance and exposure to excess exogenous glucocorticoids as main probable mechanisms. Thus, in clinical practice, CAH should be considered as one of the possible causes of brain white matter involvement associated with or without cerebral atrophy. The Japanese Society for Pediatric Endocrinology 2010-12-29 2010-10 /pmc/articles/PMC3687627/ /pubmed/23926386 http://dx.doi.org/10.1297/cpe.19.109 Text en 2010©The Japanese Society for Pediatric Endocrinology http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Case Report
Samia, Younes-Mhenni
Mahdi, Kamoun
Baha, Zantour
Saida, Jerbi-Ommezine
Tahar, Sfar Mohamed
Habib, Sfar Mohamed
Congenital Adrenal Hyperplasia and Brain Magnetic Resonance Imaging Abnormalities
title Congenital Adrenal Hyperplasia and Brain Magnetic Resonance Imaging Abnormalities
title_full Congenital Adrenal Hyperplasia and Brain Magnetic Resonance Imaging Abnormalities
title_fullStr Congenital Adrenal Hyperplasia and Brain Magnetic Resonance Imaging Abnormalities
title_full_unstemmed Congenital Adrenal Hyperplasia and Brain Magnetic Resonance Imaging Abnormalities
title_short Congenital Adrenal Hyperplasia and Brain Magnetic Resonance Imaging Abnormalities
title_sort congenital adrenal hyperplasia and brain magnetic resonance imaging abnormalities
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687627/
https://www.ncbi.nlm.nih.gov/pubmed/23926386
http://dx.doi.org/10.1297/cpe.19.109
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