ArticleInternational journal of surgery case reports2023
A case of prune belly syndrome: Experience from a regional hospital in Togo.
Article in International journal of surgery case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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2 citing papers in PubMed, 2 citations in OpenAlex.
- A case of prune belly syndrome with patent urachus: Pediatric surgical aspects of a rare case report.Radiology case reports · 2026Article
- The challenging diagnosis and management of the prune belly syndrome: A case report.SAGE open medical case reports · 2024Article
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Authors and funding
6 authors at 2 institutions in 2 countries.
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Abstract
introduction and importancePrune Belly syndrome is a rare congenital condition first reported in 1939. It is a malformative disease associated with high mortality. We report a neonatal case in a regional hospital in Togo. PRESENTATION OF CASE: A 4-month-old male infant was brought to the hospital by his uncle because of a "deformity of the abdomen and absence of testicles". The examination revealed hypoplasia of the abdominal wall associated with bilateral cryptorchidism. Abdominal and urinary tract ultrasound revealed a left pyelocaliceal dilatation and a right megaureter. All these data allowed the diagnosis of Prune Belly syndrome.
conclusionPrune Belly syndrome is a rare and complex disease with a high mortality rate.
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