The "prune belly" syndrome (PBS) combines malformation of the deferent urinary tract with cryptorchism and hypoplasia or aplasia of the abdominal musculature. Recent investigations have ascertained the role of urethral atresia or temporary urethral stenosis in the pathogenesis of PBS. The present case is classified as PBS combined with female pseudohermaphroditism and urethral atresia in a Potter syndrome. Of paradigmatic significance for the understanding of PBS pathogenesis, the case illustrates the almost exclusive occurrence of the syndrome in males, explained by the complex evolution of the phallic urethra. Hypoplasia of abdominal muscles is seen as a sequel to the extreme occupation of intraabdominal space. An alternative concept, assuming general defects in mesenchymal development that provoke independent, isolated malformations eventually subsumed under the term prune belly syndrome, is discussed in this context.
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http://dx.doi.org/10.1016/S0344-0338(83)80045-4 | DOI Listing |
J Pediatr Orthop
December 2024
Department of Orthopaedic Surgery, C.S. Mott Children's Hospital, Michigan Medicine, Ann Arbor, MI.
Background: Prune belly syndrome (PBS) is a rare condition characterized by absence of abdominal musculature, cryptorchidism, and obstructive uropathy. The most common orthopaedic problem is scoliosis, yet no reports on growth-friendly surgical treatment of early-onset scoliosis (EOS) exist. Our purpose was to evaluate outcomes of distraction-based implants in children with PBS.
View Article and Find Full Text PDFJ Paediatr Child Health
December 2024
School of Medicine, University of Tasmania, Hobart, Tasmania, Australia.
World J Urol
October 2024
Division of Pediatric Surgery, Medical Faculty and University Hospital Cologne, University of Cologne, Cologne, Germany.
Purpose: Intrauterine vesicoamniotic shunting (VAS) was shown to affect survival of male fetuses with megacystis in suspected lower urinary tract obstruction (LUTO). Data on postnatal management are largely lacking. We aim to describe the pathologies diagnosed in children born after vesicoamniotic shunt placement in early pregnancy for megacystis.
View Article and Find Full Text PDFInt J Surg Case Rep
October 2024
School of Postgraduate Studies and Research, Amoud University, Amoud Valley, Borama 25263, Somalia.
Clin Case Rep
June 2024
Institute of Medicine, Tribhuvan University Teaching Hospital Kathmandu Nepal.
Key Clinical Message: In babies presenting with an omphalocele, other components of the prune belly syndrome should be scrutinized for early diagnosis and timely intervention.
Abstract: A male baby on his 13th day of life presented with an omphalocele. On evaluation, he had congenital absence of left kidney and bilateral cryptorchidism.
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