Adrenocortical carcinoma and a sporadic MEN1 mutation in a 3-year-old girl: a case report

Childhood adrenocortical carcinoma (ACC) is a rare disease that is mostly linked to familial cancer syndrome. Although the prevalence of ACC is extremely low in children, it is clinically important to diagnose ACC early because age and tumor stage are closely related to prognosis. From this perspect...

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Detalles Bibliográficos
Autores principales: Kim, Sung Eun, Lee, Na Yeong, Cho, Won Kyoung, Yim, Jisook, Lee, Jae Wook, Kim, Myungshin, Chung, Jae Hee, Jung, Min Ho, Suh, Byung-Kyu, Ahn, Moon Bae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Pediatric Endocrinology 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816470/
https://www.ncbi.nlm.nih.gov/pubmed/35038837
http://dx.doi.org/10.6065/apem.2142100.050

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816470/
https://www.ncbi.nlm.nih.gov/pubmed/35038837
http://dx.doi.org/10.6065/apem.2142100.050

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