Mesenchymal Hamartoma of the Liver in Beckwith-Wiedemann Syndrome: The First Reported Case
| Autor: | J. De-Castro, M. T. Sotelo-Rodríguez, A. Santos-Briz, J. P. García-de-la-Torre, José Luis Rodríguez-Peralto |
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| Rok vydání: | 2000 |
| Předmět: |
Beckwith wiedemann
congenital hereditary and neonatal diseases and abnormalities Pathology medicine.medical_specialty Omphalocele business.industry Beckwith–Wiedemann syndrome General Medicine medicine.disease Mesenchymal hamartoma Pathology and Forensic Medicine Pediatrics Perinatology and Child Health Macroglossia Medicine medicine.symptom business Visceromegaly |
| Zdroj: | Fetal and Pediatric Pathology. 19:455-460 |
| ISSN: | 1551-3815 |
| DOI: | 10.3109/15513810009168652 |
| Popis: | The Beckwith-Wiedemann syndrome is a rare condition characterized by macrosomia, macroglossia, omphalocele, and visceromegaly. Although the development of neoplasia is frequent, the English literature has never described an association with mesenchymal hamartoma of the liver. We report an exceptional case of Beckwith-Wiedemann syndrome associated with a cystic mesenchymal hamartoma of the liver in a newborn. |
| Databáze: | OpenAIRE |
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