Carcinoma cortical suprarrenal pediátrico con sobreexpresión de p53

Descripción del Articulo

Adrenal cortical carcinoma is an extremely rare paediatric malignancy which usually presents with hormonal manifestations. The diagnosis is generally advanced, and the disease course is aggressive. Imaging plays a crucial role in diagnosis, preoperative planning, and staging. We present the case of...

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Detalles Bibliográficos
Autores: Tenazoa-Villalobos, José Richard, Prado-Cucho, Sofía Leonor, Bravo-Taxa, Mercedes, Yan-Quiroz, Edgar Fermín, Taxa-Rojas, Luis
Formato: artículo
Fecha de Publicación:2025
Institución:Universidad Nacional Mayor de San Marcos
Repositorio:Revistas - Universidad Nacional Mayor de San Marcos
Lenguaje:español
OAI Identifier:oai:revistasinvestigacion.unmsm.edu.pe:article/31618
Enlace del recurso:https://revistasinvestigacion.unmsm.edu.pe/index.php/anales/article/view/31618
Nivel de acceso:acceso abierto
Materia:Adrenocortical Carcinoma
Child
TP53 Gene
Immunohistochemistry
General Surgery
Carcinoma Corticosuprarrenal
Niño
Genes p53
Inmunohistoquímica
Cirugía
Descripción
Sumario:Adrenal cortical carcinoma is an extremely rare paediatric malignancy which usually presents with hormonal manifestations. The diagnosis is generally advanced, and the disease course is aggressive. Imaging plays a crucial role in diagnosis, preoperative planning, and staging. We present the case of a 7-year-old patient with a tumour that compromised the entire left renal parenchyma, with no evidence of adrenal tissue on computed tomography; the initial clinical diagnosis was Wilms tumour. However, the histopathological study reveals an adrenal cortical carcinoma with p53 overexpression; Unfortunately, the prognosis was ominous, and the patient passed away 15 months after surgery.
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