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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">El s&#237;ndrome de megavejiga-microcolon-hipoperistaltismo intestinal es una rara alteraci&#243;n gen&#233;tica caracterizada por distensi&#243;n vesical e hipoperistaltismo intestinal que afecta a todo el tracto gastrointestinal&#46; Presentamos un nuevo caso que presenta los hallazgos cl&#237;nicos y radiol&#243;gicos t&#237;picos de este s&#237;ndrome&#46; El diagn&#243;stico debe ser sospechado en un reci&#233;n nacido que presenta cl&#237;nica de obstrucci&#243;n intestinal y retenci&#243;n urinaria&#59; siendo confirmado mediante estudios de imagen&#44; fundamentalmente radiograf&#237;a simple de abdomen y ecograf&#237;a urinaria&#46; Los hallazgos histol&#243;gicos no son espec&#237;ficos&#59; encontramos un adelgazamiento de la capa muscular intestinal y proliferaci&#243;n de tejido conectivo&#46; El pron&#243;stico es generalmente grave&#46; Nuestro paciente falleci&#243; por sepsis a los 25 d&#237;as de vida&#46;</p>"
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Síndrome de megavejiga-microcolon-hipoperistaltismo intestinal
Megacystis-microcolon-intestinal hypoperistalsis syndrome
S. Rite Graciaa, B. Fernández Álvarez de Sotomayora, V. Rebage Moisésa, A. Marco Telloa, J.A. Esteban Ibarzb, M. Romeo Uleciab, M.C. Yus Gotorc, S. Rite Montañésa,
Autor para correspondencia
segundorite@jazzfree.com

Manuel Lasala, 44, 4.o C. 50006 Zaragoza
a Unidad de Neonatología. Servicio de Pediatría. Hospital Infantil Universitario Miguel Servet. Zaragoza
b Servicio de Cirugía Pediátrica. Hospital Infantil Universitario Miguel Servet. Zaragoza
c Servicio de Anatomía Patológica. Hospital Infantil Universitario Miguel Servet. Zaragoza
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        "titulo" => "Megacystis-microcolon-intestinal hypoperistalsis syndrome"
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            0 => "S&#237;ndrome de megavejiga-microcolon-hipoperistaltismointestinal"
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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">El s&#237;ndrome de megavejiga-microcolon-hipoperistaltismo intestinal es una rara alteraci&#243;n gen&#233;tica caracterizada por distensi&#243;n vesical e hipoperistaltismo intestinal que afecta a todo el tracto gastrointestinal&#46; Presentamos un nuevo caso que presenta los hallazgos cl&#237;nicos y radiol&#243;gicos t&#237;picos de este s&#237;ndrome&#46; El diagn&#243;stico debe ser sospechado en un reci&#233;n nacido que presenta cl&#237;nica de obstrucci&#243;n intestinal y retenci&#243;n urinaria&#59; siendo confirmado mediante estudios de imagen&#44; fundamentalmente radiograf&#237;a simple de abdomen y ecograf&#237;a urinaria&#46; Los hallazgos histol&#243;gicos no son espec&#237;ficos&#59; encontramos un adelgazamiento de la capa muscular intestinal y proliferaci&#243;n de tejido conectivo&#46; El pron&#243;stico es generalmente grave&#46; Nuestro paciente falleci&#243; por sepsis a los 25 d&#237;as de vida&#46;</p>"
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        "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Megacystis-microcolon-intestinal hypoperistalsis is a rare congenital disorder characterized by urinary bladder distention and hypoperistalsis throughout the entire gastrointestinal tract&#46; We present a new case with the typical clinical and radiological findings of the syndrome&#46; This diagnosis should be suspected in patients who present with intestinal obstruction and urine retention and should be confirmed with imaging techniques&#44; including abdominal plain films and urinary ultrasonography&#46; Histological findings are non-specific&#59; we found thinning of the intestinal muscle layer and connective tissue proliferation&#46; The prognosis is generally very poor&#46; Our patient died from sepsis at the age of 25 days&#46;</p>"
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Información del artículo
ISSN: 16954033
Idioma original: Español
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