Poliposis múltiple juvenil no familiar: Caso clínico

We report a 15 years old girl presenting with severe hematochezia with secondary anemia and hemodynamic decompensation, rectal prolapse and spontaneous anal elimination of polyps. She had no family history of polyposis and a search for the disease in her close relatives was negative. A complete diag...

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Autores principales:	Bannura C,Guillermo, Soto C,Daniel, Vial P,María Teresa
Lenguaje:	Spanish / Castilian
Publicado:	Sociedad Médica de Santiago 2001
Materias:	Adenomatous polyposes coli Colonic polyps Colonoscopy
Acceso en línea:	http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872001000900014
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spelling	oai:scielo:S0034-988720010009000142005-11-24Poliposis múltiple juvenil no familiar: Caso clínicoBannura C,GuillermoSoto C,DanielVial P,María Teresa Adenomatous polyposes coli Colonic polyps Colonoscopy We report a 15 years old girl presenting with severe hematochezia with secondary anemia and hemodynamic decompensation, rectal prolapse and spontaneous anal elimination of polyps. She had no family history of polyposis and a search for the disease in her close relatives was negative. A complete diagnostic work up did not find polyps in other segments of the digestive tract. Colonoscopy showed more than 200 polyps between the cecum and the rectum. Pathological analysis confirmed the presence of retention polyps with adenomatous areas and mild atypia. The patient was subjected to a proctocolectomy with ileal pouch and sphincteric preservation, using a mechanical suture. Postoperative evolution was uneventful and after 24 months of follow up, the patient is asymptomatic, with two stool movements per day and without incontinence (Rev Méd Chile 2001; 129: 1065-70)info:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.129 n.9 20012001-09-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872001000900014es10.4067/S0034-98872001000900014
institution	Scielo Chile
collection	Scielo Chile
language	Spanish / Castilian
topic	Adenomatous polyposes coli Colonic polyps Colonoscopy
spellingShingle	Adenomatous polyposes coli Colonic polyps Colonoscopy Bannura C,Guillermo Soto C,Daniel Vial P,María Teresa Poliposis múltiple juvenil no familiar: Caso clínico
description	We report a 15 years old girl presenting with severe hematochezia with secondary anemia and hemodynamic decompensation, rectal prolapse and spontaneous anal elimination of polyps. She had no family history of polyposis and a search for the disease in her close relatives was negative. A complete diagnostic work up did not find polyps in other segments of the digestive tract. Colonoscopy showed more than 200 polyps between the cecum and the rectum. Pathological analysis confirmed the presence of retention polyps with adenomatous areas and mild atypia. The patient was subjected to a proctocolectomy with ileal pouch and sphincteric preservation, using a mechanical suture. Postoperative evolution was uneventful and after 24 months of follow up, the patient is asymptomatic, with two stool movements per day and without incontinence (Rev Méd Chile 2001; 129: 1065-70)
author	Bannura C,Guillermo Soto C,Daniel Vial P,María Teresa
author_facet	Bannura C,Guillermo Soto C,Daniel Vial P,María Teresa
author_sort	Bannura C,Guillermo
title	Poliposis múltiple juvenil no familiar: Caso clínico
title_short	Poliposis múltiple juvenil no familiar: Caso clínico
title_full	Poliposis múltiple juvenil no familiar: Caso clínico
title_fullStr	Poliposis múltiple juvenil no familiar: Caso clínico
title_full_unstemmed	Poliposis múltiple juvenil no familiar: Caso clínico
title_sort	poliposis múltiple juvenil no familiar: caso clínico
publisher	Sociedad Médica de Santiago
publishDate	2001
url	http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872001000900014
work_keys_str_mv	AT bannuracguillermo poliposismultiplejuvenilnofamiliarcasoclinico AT sotocdaniel poliposismultiplejuvenilnofamiliarcasoclinico AT vialpmariateresa poliposismultiplejuvenilnofamiliarcasoclinico
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Poliposis múltiple juvenil no familiar: Caso clínico

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