NEUROBLASTOMA IN A CASE OF CONGENITAL ADRENAL HYPERPLASIA

Case report: The majority of neuroblastomas are sporadic and not correlated with any specific constitutional germline chromosomal abnormality, inherited predisposition, or associated congenital anomalies. We report here a 1.5-year-old girl with a diagnosis of 21 hydroxylase deficiency and neuroblast...

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Autores principales:	Arzu Yazal Erdem, Sonay İncesoy Özdemir, Meriç Kamak Cihan, Derya Özyörük, Neriman Sarı, İnci Ergürhan İlhan
Formato:	article
Lenguaje:	EN
Publicado:	Elsevier 2021
Materias:	Diseases of the blood and blood-forming organs RC633-647.5
Acceso en línea:	https://doaj.org/article/cee89370fff643b4b8e840f231a259ba
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spelling	oai:doaj.org-article:cee89370fff643b4b8e840f231a259ba2021-11-10T04:34:11ZNEUROBLASTOMA IN A CASE OF CONGENITAL ADRENAL HYPERPLASIA2531-137910.1016/j.htct.2021.10.1005https://doaj.org/article/cee89370fff643b4b8e840f231a259ba2021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2531137921011524https://doaj.org/toc/2531-1379Case report: The majority of neuroblastomas are sporadic and not correlated with any specific constitutional germline chromosomal abnormality, inherited predisposition, or associated congenital anomalies. We report here a 1.5-year-old girl with a diagnosis of 21 hydroxylase deficiency and neuroblastoma. Neuroblastoma in a known case of congenital adrenal hyperplasia has rarely been reported. Based on our literature review, this is the fifth case report of congenital adrenal hyperplasia and neuroblastoma.Arzu Yazal ErdemSonay İncesoy ÖzdemirMeriç Kamak CihanDerya ÖzyörükNeriman Sarıİnci Ergürhan İlhanElsevierarticleDiseases of the blood and blood-forming organsRC633-647.5ENHematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S30- (2021)
institution	DOAJ
collection	DOAJ
language	EN
topic	Diseases of the blood and blood-forming organs RC633-647.5
spellingShingle	Diseases of the blood and blood-forming organs RC633-647.5 Arzu Yazal Erdem Sonay İncesoy Özdemir Meriç Kamak Cihan Derya Özyörük Neriman Sarı İnci Ergürhan İlhan NEUROBLASTOMA IN A CASE OF CONGENITAL ADRENAL HYPERPLASIA
description	Case report: The majority of neuroblastomas are sporadic and not correlated with any specific constitutional germline chromosomal abnormality, inherited predisposition, or associated congenital anomalies. We report here a 1.5-year-old girl with a diagnosis of 21 hydroxylase deficiency and neuroblastoma. Neuroblastoma in a known case of congenital adrenal hyperplasia has rarely been reported. Based on our literature review, this is the fifth case report of congenital adrenal hyperplasia and neuroblastoma.
format	article
author	Arzu Yazal Erdem Sonay İncesoy Özdemir Meriç Kamak Cihan Derya Özyörük Neriman Sarı İnci Ergürhan İlhan
author_facet	Arzu Yazal Erdem Sonay İncesoy Özdemir Meriç Kamak Cihan Derya Özyörük Neriman Sarı İnci Ergürhan İlhan
author_sort	Arzu Yazal Erdem
title	NEUROBLASTOMA IN A CASE OF CONGENITAL ADRENAL HYPERPLASIA
title_short	NEUROBLASTOMA IN A CASE OF CONGENITAL ADRENAL HYPERPLASIA
title_full	NEUROBLASTOMA IN A CASE OF CONGENITAL ADRENAL HYPERPLASIA
title_fullStr	NEUROBLASTOMA IN A CASE OF CONGENITAL ADRENAL HYPERPLASIA
title_full_unstemmed	NEUROBLASTOMA IN A CASE OF CONGENITAL ADRENAL HYPERPLASIA
title_sort	neuroblastoma in a case of congenital adrenal hyperplasia
publisher	Elsevier
publishDate	2021
url	https://doaj.org/article/cee89370fff643b4b8e840f231a259ba
work_keys_str_mv	AT arzuyazalerdem neuroblastomainacaseofcongenitaladrenalhyperplasia AT sonayincesoyozdemir neuroblastomainacaseofcongenitaladrenalhyperplasia AT merickamakcihan neuroblastomainacaseofcongenitaladrenalhyperplasia AT deryaozyoruk neuroblastomainacaseofcongenitaladrenalhyperplasia AT nerimansarı neuroblastomainacaseofcongenitaladrenalhyperplasia AT inciergurhanilhan neuroblastomainacaseofcongenitaladrenalhyperplasia
_version_	1718440694231597056

NEUROBLASTOMA IN A CASE OF CONGENITAL ADRENAL HYPERPLASIA

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