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A Metadata Extraction Approach for Clinical Case Reports to Enable Advanced Understanding of Biomedical Concepts
Published on: September 20, 2018
[Cantrell's pentalogy. Four cases reported]
Carlos Baeza-Herrera1, Moisés A Escobar-Izquierdo, Luis Manuel García-Cabello
1Hospital Pediátrico Moctezuma, Secretaría de Salud, Distrito Federal, México. cirpolosm@yahoo.com
Revista Medica Del Instituto Mexicano Del Seguro Social
|March 7, 2009
Summary
Cantrell's pentalogy is a rare neonatal condition. Early detection and surgical planning are crucial for improving outcomes in affected infants.
Area of Science:
- Neonatal surgery
- Pediatric cardiology
- Congenital anomalies
Background:
- Cantrell's pentalogy is a rare syndrome described in 1958.
- Characterized by a midline supraumbilical defect, thoracoabdominal omphalocele, ectopia cordis, sternal defects, and cardiac anomalies.
Observation:
- A case series of 4 neonates with Cantrell's pentalogy over a 5-year period.
- No apparent common factors were identified among the affected neonates.
- The clinical course and surgical correction strategies were documented.
Findings:
- The study details the presentation and management of 4 neonates with Cantrell's pentalogy.
- Surgical correction was performed, with outcomes and clinical courses described.
- Highlights the rarity and complexity of this congenital condition.
Implications:
- Early detection of Cantrell's pentalogy is vital for diagnosis.
- Effective surgical planning is essential for patient management.
- Timely intervention significantly impacts prognostic outcomes.
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