Carcinosarcoma with choriocarcinomatous and osteosarcomatous differentiation in a patient with juvenile polyposis syndrome

Juvenile polyposis syndrome (JPS) is an infrequent autosomal dominant hereditary predisposition to the occurrence of hamartomatous polyps in the colon and rectum. We describe the case of a 12-year-old boy with JPS associated with an abdominal tumor. Histological sections of the abdominal tumor showe...

Full description

Autores:

López Correa, Patricia
Jiménez Moreno, Julián
Moreno Lucero, Paula
Yaspe, Edgardo
Polo Nieto, José Fernando
Parra-Medina, Rafael

Tipo de recurso:

Article of journal

Fecha de publicación:

2015

Institución:

Fundación Universitaria de Ciencias de la Salud - FUCS

Repositorio:

Repositorio Digital Institucional ReDi

Idioma:

eng

OAI Identifier:

oai:repositorio.fucsalud.edu.co:001/1402

Acceso en línea:

https://doi.org/10.4081/rt.2015.5778
https://repositorio.fucsalud.edu.co/handle/001/1402

Palabra clave:

Juvenile polyposis syndrome
choriocarcinoma
Adenocarcinoma
Osteosarcoma
Coriocarcinoma

Rights

openAccess

License

Atribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)