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Pentalogy of cantrell with complete ectopia cordis in a fetus with asplenia.
Ludwig, Kathrin; Salmaso, Roberto; Cosmi, Erich; Iaria, Loredana; De Luca, Alessandro; Margiotti, Katia; Valentina, Citton; Manara, Renzo; Rugge, Massimo.
Afiliación
  • Ludwig K; Department of Medicine (DIMED), Surgical Pathology and Cytopathology Unit, University of Padova, Padova, Italy.
Pediatr Dev Pathol ; 15(6): 495-8, 2012.
Article en En | MEDLINE | ID: mdl-22900993
Cantrell's pentalogy (CP) is a rare, mainly sporadic spectrum of congenital midline thoracoabdominal defects that includes sternal anomalies, ventral diaphragmatic hernia, partial absence of the pericardium, supraumbilical abdominal wall defects, and congenital heart malformations. The approximate incidence is 1 in 100 000, with a 2∶1 male predominance. A 25-year-old pregnant woman was referred to the Prenatal Diagnosis Unit of the University Hospital of Padua for multiple congenital malformations at 21 weeks of gestation. A level 2 ultrasound scan was performed and confirmed the presence of multiple anomalies compatible with the diagnosis of CP associated with complete ectopia cordis. Fetal autopsy furthermore revealed asplenia, which usually presents as part of the heterotaxia spectrum. To our knowledge, an association of CP and complete ectopia cordis with asplenia has never been reported so far.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Bazo / Ectopía Cordis / Pentalogía de Cantrell Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Pediatr Dev Pathol Asunto de la revista: PATOLOGIA / PEDIATRIA Año: 2012 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Bazo / Ectopía Cordis / Pentalogía de Cantrell Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Pediatr Dev Pathol Asunto de la revista: PATOLOGIA / PEDIATRIA Año: 2012 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos