Pancreatoblastoma. Reporte de casos y revisión bibliográfica

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1. Verfasser: Carla Pennella
Format: Artículo científico
Sprache:en
Veröffentlicht: Sociedad Argentina de Gastroenterología 2020
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author Carla Pennella
author_facet Carla Pennella
contents Pancreatoblastoma. Reporte de casos y revisión bibliográfica Carla Pennella Andrea Bosaleh Adriana Rose Pedro Zubizarreta Walter Cacciavillano Medicina children treatment rare tumors pancreatic tumor Pancreatoblastoma Although pancreatoblastoma (PB) is a rare tumor, it is the most common malignant pancreatic tumor in children. Clinic presentation is insidious, so early diagnostic suspicion allows timely therapy. We reported 3 cases of PB treated at our center. The first two cases achieved complete disease response after full tumor resection. The first one is in complete remission at 7 months after chemotherapy. The second patient is in second complete remission at 206 months after diagnosis and 128 months after metastatic relapse. The third case died from disease progression 61 months after the initial metastatic unresectable tumor. Histology, clinical features and treatment options are discussed along with presentation of the cases. 2020 artículo científico 2469-1119 https://www.redalyc.org/articulo.oa?id=199363471015 https://www.redalyc.org/journal/1993/199363471015/ https://www.redalyc.org/journal/1993/199363471015/html/ https://www.redalyc.org/journal/1993/199363471015/199363471015.epub https://www.redalyc.org/journal/1993/199363471015/movil en http://www.redalyc.org/revista.oa?id=1993 Acta Gastroenterológica Latinoamericana application/pdf Sociedad Argentina de Gastroenterología Acta Gastroenterológica Latinoamericana (Argentina) Num.2 Vol.50
format Artículo científico
id redalyc_199363471015
institution Redalyc
language en
publishDate 2020
publisher Sociedad Argentina de Gastroenterología
spellingShingle Pancreatoblastoma. Reporte de casos y revisión bibliográfica
Carla Pennella
Medicina
children
treatment
rare tumors
pancreatic tumor
Pancreatoblastoma
Pancreatoblastoma. Reporte de casos y revisión bibliográfica Carla Pennella Andrea Bosaleh Adriana Rose Pedro Zubizarreta Walter Cacciavillano Medicina children treatment rare tumors pancreatic tumor Pancreatoblastoma Although pancreatoblastoma (PB) is a rare tumor, it is the most common malignant pancreatic tumor in children. Clinic presentation is insidious, so early diagnostic suspicion allows timely therapy. We reported 3 cases of PB treated at our center. The first two cases achieved complete disease response after full tumor resection. The first one is in complete remission at 7 months after chemotherapy. The second patient is in second complete remission at 206 months after diagnosis and 128 months after metastatic relapse. The third case died from disease progression 61 months after the initial metastatic unresectable tumor. Histology, clinical features and treatment options are discussed along with presentation of the cases. 2020 artículo científico 2469-1119 https://www.redalyc.org/articulo.oa?id=199363471015 https://www.redalyc.org/journal/1993/199363471015/ https://www.redalyc.org/journal/1993/199363471015/html/ https://www.redalyc.org/journal/1993/199363471015/199363471015.epub https://www.redalyc.org/journal/1993/199363471015/movil en http://www.redalyc.org/revista.oa?id=1993 Acta Gastroenterológica Latinoamericana application/pdf Sociedad Argentina de Gastroenterología Acta Gastroenterológica Latinoamericana (Argentina) Num.2 Vol.50
title Pancreatoblastoma. Reporte de casos y revisión bibliográfica
topic Medicina
children
treatment
rare tumors
pancreatic tumor
Pancreatoblastoma
url https://www.redalyc.org/articulo.oa?id=199363471015
https://www.redalyc.org/journal/1993/199363471015/
https://www.redalyc.org/journal/1993/199363471015/html/
https://www.redalyc.org/journal/1993/199363471015/199363471015.epub
https://www.redalyc.org/journal/1993/199363471015/movil