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A 15-Year-Old With Tetralogy of Fallot With Pulmonic Atresia, Multiple Aorticopulmonary Collateral Arteries and Bilateral Peripheral Pulmonary Stenosis
Tetralogy of Fallot (TOF) is a congenital disorder comprised of four heart defects. It is considered a critical condition that requires surgical repair. TOF may be complicated by pulmonary valve atresia (PA) and the development of major aorticopulmonary collateral arteries (MAPCA). A 15-year-old gir...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7686929/ https://www.ncbi.nlm.nih.gov/pubmed/33251060 http://dx.doi.org/10.7759/cureus.11151 |
Sumario: | Tetralogy of Fallot (TOF) is a congenital disorder comprised of four heart defects. It is considered a critical condition that requires surgical repair. TOF may be complicated by pulmonary valve atresia (PA) and the development of major aorticopulmonary collateral arteries (MAPCA). A 15-year-old girl from Jimma, Ethiopia, was admitted to the pediatric cardiology unit through the "Save a Child's Heart" organization. She was diagnosed at the age of four years with TOF but had not yet received treatment for the condition. Echocardiography prompted a diagnosis of TOF with PA and MAPCA. It is recommended that TOF be treated shortly after birth, thus observing this condition in 15-year-old highlights the complications that may accompany delayed repair. This report details the course of diagnosis and treatment for this patient. |
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