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Clinical, Genetic, and Prognostic Features of Adrenocortical Tumors in Children: A 10-Year Single-Center Experience

Background and Aims: Pediatric adrenocortical tumors (ACTs) are very rare endocrine neoplasms in childhood. In this study, we performed a retrospective analysis of children with ACT treated at our institution by examining clinical and genetic disease features, treatment strategies, and outcomes. Met...

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Vydáno v:Front Oncol
Hlavní autoři: Miele, Evelina, Di Giannatale, Angela, Crocoli, Alessandro, Cozza, Raffaele, Serra, Annalisa, Castellano, Aurora, Cacchione, Antonella, Cefalo, Maria Giuseppina, Alaggio, Rita, De Pasquale, Maria Debora
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2020
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7593337/
https://ncbi.nlm.nih.gov/pubmed/33178583
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fonc.2020.554388
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