Management of a Composite Pheochromocytoma (Pheochromocytoma/Neuroblastoma) in Adult Patient Recurring After Several Years: A Complex Case Report.
J Adolesc Young Adult Oncol
; 12(4): 604-610, 2023 08.
Article
em En
| MEDLINE
| ID: mdl-36169643
ABSTRACT
Pheochromocytoma/neuroblastoma composite tumors are rare entities for which little is known. We report an atypical case of a 39-year-old man with secondary bone locations of a composite tumor, 7 years after resection of adrenal neuroblastoma, with constitutional alteration of SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily A, member 4 whose role is unknown. The diagnosis of a peripheral neuroblastic tumor in adulthood is difficult and even more so when it is a composite tumor. In the absence of a standard of care, management is varied and discussions about treatment modalities for these patients are complex.
Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Feocromocitoma
/
Neoplasias das Glândulas Suprarrenais
/
Neuroblastoma
Limite:
Adult
/
Humans
/
Male
Idioma:
En
Revista:
J Adolesc Young Adult Oncol
Ano de publicação:
2023
Tipo de documento:
Article
País de afiliação:
França