A concurrent episode of two neoplasms in a toddler-age child

Childhood neoplasms are relatively rare and represent only about 1- 2% of the total incidence of neoplasms in United States. Concurrent episode of childhood cancer is uncommon and usually related to a cancer genetic syndrome. Li Fraumeni Syndrome refers to an autosomal dominant condition that is man...

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Autores principales:	Muaz A Alrazzak, Jenny ZablahAlabi, Baraa Alrazzak, Guillermo De Angulo
Formato:	article
Lenguaje:	EN
Publicado:	Thieme Medical and Scientific Publishers Pvt. Ltd. 2014
Materias:	adrenocortical tumor li fraumeni syndrome orbital rhabdomyosarcoma Medicine R
Acceso en línea:	https://doaj.org/article/c761c4bbf36d4125bd0bfd634ee7e7e9
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spelling	oai:doaj.org-article:c761c4bbf36d4125bd0bfd634ee7e7e92021-12-02T16:24:52ZA concurrent episode of two neoplasms in a toddler-age child2231-07702249-446410.4103/2231-0770.130347https://doaj.org/article/c761c4bbf36d4125bd0bfd634ee7e7e92014-04-01T00:00:00Zhttp://www.thieme-connect.de/DOI/DOI?10.4103/2231-0770.130347https://doaj.org/toc/2231-0770https://doaj.org/toc/2249-4464Childhood neoplasms are relatively rare and represent only about 1- 2% of the total incidence of neoplasms in United States. Concurrent episode of childhood cancer is uncommon and usually related to a cancer genetic syndrome. Li Fraumeni Syndrome refers to an autosomal dominant condition that is manifested by the development of certain cancers in early childhood and an increased lifetime risk for developing multiple primary cancers including sarcoma, breast cancer, leukemia, bone cancer, and others. We report a case of a 21-month-old girl who was found to have orbital embryonal rhabdomyosarcoma and adrenocortical tumor concurrently.Muaz A AlrazzakJenny ZablahAlabiBaraa AlrazzakGuillermo De AnguloThieme Medical and Scientific Publishers Pvt. Ltd.articleadrenocortical tumorli fraumeni syndromeorbital rhabdomyosarcomaMedicineRENAvicenna Journal of Medicine, Vol 04, Iss 02, Pp 48-50 (2014)
institution	DOAJ
collection	DOAJ
language	EN
topic	adrenocortical tumor li fraumeni syndrome orbital rhabdomyosarcoma Medicine R
spellingShingle	adrenocortical tumor li fraumeni syndrome orbital rhabdomyosarcoma Medicine R Muaz A Alrazzak Jenny ZablahAlabi Baraa Alrazzak Guillermo De Angulo A concurrent episode of two neoplasms in a toddler-age child
description	Childhood neoplasms are relatively rare and represent only about 1- 2% of the total incidence of neoplasms in United States. Concurrent episode of childhood cancer is uncommon and usually related to a cancer genetic syndrome. Li Fraumeni Syndrome refers to an autosomal dominant condition that is manifested by the development of certain cancers in early childhood and an increased lifetime risk for developing multiple primary cancers including sarcoma, breast cancer, leukemia, bone cancer, and others. We report a case of a 21-month-old girl who was found to have orbital embryonal rhabdomyosarcoma and adrenocortical tumor concurrently.
format	article
author	Muaz A Alrazzak Jenny ZablahAlabi Baraa Alrazzak Guillermo De Angulo
author_facet	Muaz A Alrazzak Jenny ZablahAlabi Baraa Alrazzak Guillermo De Angulo
author_sort	Muaz A Alrazzak
title	A concurrent episode of two neoplasms in a toddler-age child
title_short	A concurrent episode of two neoplasms in a toddler-age child
title_full	A concurrent episode of two neoplasms in a toddler-age child
title_fullStr	A concurrent episode of two neoplasms in a toddler-age child
title_full_unstemmed	A concurrent episode of two neoplasms in a toddler-age child
title_sort	concurrent episode of two neoplasms in a toddler-age child
publisher	Thieme Medical and Scientific Publishers Pvt. Ltd.
publishDate	2014
url	https://doaj.org/article/c761c4bbf36d4125bd0bfd634ee7e7e9
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A concurrent episode of two neoplasms in a toddler-age child

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