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...

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Detalles Bibliográficos
Autores principales: Parra-Medina, Rafael, Correa, Patricia López, Moreno, Julian Jiménez, Lucero, Paula Moreno, Yaspe, Edgardo, Polo, Fernando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600986/
https://www.ncbi.nlm.nih.gov/pubmed/26500724
http://dx.doi.org/10.4081/rt.2015.5778

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600986/
https://www.ncbi.nlm.nih.gov/pubmed/26500724
http://dx.doi.org/10.4081/rt.2015.5778

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