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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japanese Society for Pediatric Endocrinology
2010
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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. |
format | Online Article Text |
id | pubmed-3687627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Japanese Society for Pediatric Endocrinology |
record_format | MEDLINE/PubMed |
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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