Pentalogy of Fallot with Anorectal Malformation: A Case Report.
Autor: | Maharjan SR; Neonatology Division, Department of Pediatrics, Kathmandu Medical College and Teaching Hospital, Kathmandu, Nepal., Kafle P; Department of Radiology0, Kathmandu Medical College and Teaching Hospital, Kathmandu, Nepal., Shrestha AL; Department of Pediatrics Surgery, Kathmandu Medical College and Teaching Hospital, Kathmandu, Nepal., Rai D; Neonatology division, Department of Pediatrics, Kathmandu Medical College and Teaching Hospital, Kathmandu, Nepal. |
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Jazyk: | angličtina |
Zdroj: | JNMA; journal of the Nepal Medical Association [JNMA J Nepal Med Assoc] 2024 Jul 31; Vol. 62 (276), pp. 542-544. Date of Electronic Publication: 2024 Jul 31. |
DOI: | 10.31729/jnma.8705 |
Abstrakt: | Abstract: Pentalogy of Fallot is a rare form of congenital cyanotic heart disease with a prevalence of 3/10,000 live births characterized by an association of Tetralogy of Fallot with Atrial Septal Defect. Pentalogy of Fallot with anorectal malformation is also a rare combination. Here we describe one of the rare case reports of a full-term, 38 weeks, female baby diagnosed with pentalogy of Fallot with imperforate anus and rectovaginal fistula at a tertiary care hospital. Pentalogy of Fallot combined with an imperforate anus and rectovaginal fistula is an exceptionally rare and complex congenital condition. The co- existence of these anomalies emphasizes the need for thorough prenatal and postnatal evaluation for early detection and management. |
Databáze: | MEDLINE |
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