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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">La aplasia cutis cong&#233;nita es una rara alteraci&#243;n caracterizada por la ausencia cong&#233;nita de epidermis&#44; dermis y&#44; en ocasiones&#44; de los tejidos subyacentes&#46; Fue descrita por primera vez por Cordon en 1767 y desde entonces se han referido unos 500 casos&#44; con una incidencia estimada de 3 de cada 10&#46;000 reci&#233;n nacidos&#46; Las lesiones pueden afectar a cualquier regi&#243;n corporal&#44; aunque la localizaci&#243;n m&#225;s frecuente es en el cuero cabelludo&#46; En aproximadamente un 20&#37; de los casos se encuentra un defecto &#243;seo del cr&#225;neo subyacente&#46; La aplasia cutis cong&#233;nita puede presentarse aislada o asociada a otras malformaciones&#46; No hay una teor&#237;a etiopatog&#233;nica uniforme y los grandes defectos del cuero cabelludo plantean un dilema terap&#233;utico&#46; Presentamos un reci&#233;n nacido con un extenso defecto de cuero cabelludo localizado en la l&#237;nea media del v&#233;rtex sin otras malformaciones asociadas&#46; No exist&#237;an antecedentes familiares de inter&#233;s&#46; Las radiograf&#237;as de cr&#225;neo y extremidades&#44; el an&#225;lisis cromos&#243;mico y las ecograf&#237;as cerebral y abdominal fueron normales&#46; Se emplearon dos pautas terap&#233;uticas&#58; un tratamiento conservador&#44; consistente en curas locales diarias con antis&#233;pticos para permitir la epitelizaci&#243;n&#44; mejor&#243; las condiciones para el tratamiento quir&#250;rgico secundario&#44; cerrando el defecto a los 30 d&#237;as de vida con colgajos rotacionales locales&#46; El postoperatorio curs&#243; sin incidencias y se consigui&#243; un excelente resultado est&#233;tico&#46;</p>"
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        "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Aplasia cutis congenita is a rare condition characterized by the congenital absence of epidermis&#44; dermis and&#44; in some cases&#44; subcutaneous tissues&#46; It was first described by Cordon in 1767 and more than 500 cases have been reported since&#44; with an estimate incidence of 3 in 10&#44;000 births&#46; The lesions may occur on any body surface although localised agenesis of the scalp is the most frequent pattern&#46; In approximately 20&#37; of cases underlying bone defects are also found&#46; Aplasia cutis congenita occurs as an isolated defect or with other associated anomalies&#46; There is no unifying theory for the pathogenesis and large scalp defects present a management dilemma&#46; We report a newborn with a large scalp defect in the mid line retiesradiographs&#44; chromosome analysis&#44; cerebral and abdominal sonography were normal&#46; Two methods of treatment were used&#58; a conservative approach consisting of daily antiseptic dressing to allow scalp epithelialization improved conditions for secondary surgery at 30 The postoperative course was uneventful and an excellent cosmetic result was achieved&#46;</p>"
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Aplasia cutis congénita en un recién nacido: revisión etiopatogénica y actitud diagnóstica
Aplasia cutis congenita in a newborn: Etiopathogenic review and diagnostic attitude
M. Moros Peña*, M. Labay Matías, F. Valle Sánchez, T. Valero Adán, J. Martín-Calama Valero, M. Muñoz Albillos
Servicio de Pediatría. Hospital General de Teruel Obispo Polanco. Teruel
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    "titulo" => "Aplasia cutis cong&#233;nita en un reci&#233;n nacido&#58; revisi&#243;n etiopatog&#233;nica y actitud diagn&#243;stica"
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        "titulo" => "Aplasia cutis congenita in a newborn&#58; Etiopathogenic review and diagnostic attitude"
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            1 => "Reci&#233;n nacido"
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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">La aplasia cutis cong&#233;nita es una rara alteraci&#243;n caracterizada por la ausencia cong&#233;nita de epidermis&#44; dermis y&#44; en ocasiones&#44; de los tejidos subyacentes&#46; Fue descrita por primera vez por Cordon en 1767 y desde entonces se han referido unos 500 casos&#44; con una incidencia estimada de 3 de cada 10&#46;000 reci&#233;n nacidos&#46; Las lesiones pueden afectar a cualquier regi&#243;n corporal&#44; aunque la localizaci&#243;n m&#225;s frecuente es en el cuero cabelludo&#46; En aproximadamente un 20&#37; de los casos se encuentra un defecto &#243;seo del cr&#225;neo subyacente&#46; La aplasia cutis cong&#233;nita puede presentarse aislada o asociada a otras malformaciones&#46; No hay una teor&#237;a etiopatog&#233;nica uniforme y los grandes defectos del cuero cabelludo plantean un dilema terap&#233;utico&#46; Presentamos un reci&#233;n nacido con un extenso defecto de cuero cabelludo localizado en la l&#237;nea media del v&#233;rtex sin otras malformaciones asociadas&#46; No exist&#237;an antecedentes familiares de inter&#233;s&#46; Las radiograf&#237;as de cr&#225;neo y extremidades&#44; el an&#225;lisis cromos&#243;mico y las ecograf&#237;as cerebral y abdominal fueron normales&#46; Se emplearon dos pautas terap&#233;uticas&#58; un tratamiento conservador&#44; consistente en curas locales diarias con antis&#233;pticos para permitir la epitelizaci&#243;n&#44; mejor&#243; las condiciones para el tratamiento quir&#250;rgico secundario&#44; cerrando el defecto a los 30 d&#237;as de vida con colgajos rotacionales locales&#46; El postoperatorio curs&#243; sin incidencias y se consigui&#243; un excelente resultado est&#233;tico&#46;</p>"
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        "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Aplasia cutis congenita is a rare condition characterized by the congenital absence of epidermis&#44; dermis and&#44; in some cases&#44; subcutaneous tissues&#46; It was first described by Cordon in 1767 and more than 500 cases have been reported since&#44; with an estimate incidence of 3 in 10&#44;000 births&#46; The lesions may occur on any body surface although localised agenesis of the scalp is the most frequent pattern&#46; In approximately 20&#37; of cases underlying bone defects are also found&#46; Aplasia cutis congenita occurs as an isolated defect or with other associated anomalies&#46; There is no unifying theory for the pathogenesis and large scalp defects present a management dilemma&#46; We report a newborn with a large scalp defect in the mid line retiesradiographs&#44; chromosome analysis&#44; cerebral and abdominal sonography were normal&#46; Two methods of treatment were used&#58; a conservative approach consisting of daily antiseptic dressing to allow scalp epithelialization improved conditions for secondary surgery at 30 The postoperative course was uneventful and an excellent cosmetic result was achieved&#46;</p>"
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ISSN: 16954033
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