Challenges in the surgical treatment of a 8-year old child living with Prune Belly syndrome: case report
DOI:
https://doi.org/10.36311/jhgd.v33.13793Keywords:
Prune Belly Syndrome, eagle-barrett syndrome, Monford abdominoplasty, case reportAbstract
Prune Belly syndrome, also known as Eagle-Barret syndrome, is a rare disease, with a prevalence of 3.8 live births per 100,000 births. Its main characteristic is the hypoplasia of the abdominal muscles, giving rise to the name “prune belly syndrome”. The gold standard treatment is surgery, ideally with correction of cryptorchidism and phimosis between 6 to 18 months of life. Correction of urinary malformations and abdominoplasty should be performed up to 4 years of age. Little evidence exists in the literature about late treatment and its implications for prognosis. The context mentioned above led us to present an uncommon case of a six years old child in which a surgical approach was performed later than usual.
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Copyright (c) 2022 Trivilato RA, Dadalt G, Assenço DL, Barbalho DF, Costa MR, Chater N, Lima RR, Barreira BMA, Teixeira JPB, Cruvinel F, Figueiredo JL
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