The prune belly syndrome: report of a rare case and review of literature

The prune belly syndrome: report of a rare case and review of literature Eur J Plast Surg (2012) 35:241–243 DOI 10.1007/s00238-010-0525-2 CASE REPORT The prune belly syndrome: report of a rare case and review of literature Kristoff Verdonck & Gregory Van Eeckhout & Veerle De Boe & Paul Wylock Received: 12 April 2010 /Accepted: 17 October 2010 /Published online: 28 January 2011 Springer-Verlag 2010 Introduction urinary tract causing a dilatation of the bladder and, secondary to this situation, a pressure atrophy of the The prune belly syndrome (PBS) is a rare birth disorder abdominal muscles. Although very plausible, his theory characterized by three major findings: a variable aplasia of was countered by histopathological investigation of the the abdominal wall, urinary tract malformations, and abdominal wall which revealed that there was no atrophy cryptorchidism [1–3]. The syndrome was first described but rather a developmental arrest of the muscle. by Frölich in 1839 [1], but it was not until 1901 that the A more recent theory is that of a mesenchymal condition was named by Ösler [2]. The syndrome got its development arrest between the sixth to tenth week of descriptive name due to the wrinkled abdominal skin (the gestation [6, 13]. This could also explain the involvement intestinal pattern is evident through the http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png European Journal of Plastic Surgery Springer Journals

The prune belly syndrome: report of a rare case and review of literature

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Publisher
Springer Journals
Copyright
Copyright © 2012 by Springer-Verlag
Subject
Medicine & Public Health; Plastic Surgery
ISSN
0930-343X
eISSN
1435-0130
D.O.I.
10.1007/s00238-010-0525-2
Publisher site
See Article on Publisher Site

Abstract

Eur J Plast Surg (2012) 35:241–243 DOI 10.1007/s00238-010-0525-2 CASE REPORT The prune belly syndrome: report of a rare case and review of literature Kristoff Verdonck & Gregory Van Eeckhout & Veerle De Boe & Paul Wylock Received: 12 April 2010 /Accepted: 17 October 2010 /Published online: 28 January 2011 Springer-Verlag 2010 Introduction urinary tract causing a dilatation of the bladder and, secondary to this situation, a pressure atrophy of the The prune belly syndrome (PBS) is a rare birth disorder abdominal muscles. Although very plausible, his theory characterized by three major findings: a variable aplasia of was countered by histopathological investigation of the the abdominal wall, urinary tract malformations, and abdominal wall which revealed that there was no atrophy cryptorchidism [1–3]. The syndrome was first described but rather a developmental arrest of the muscle. by Frölich in 1839 [1], but it was not until 1901 that the A more recent theory is that of a mesenchymal condition was named by Ösler [2]. The syndrome got its development arrest between the sixth to tenth week of descriptive name due to the wrinkled abdominal skin (the gestation [6, 13]. This could also explain the involvement intestinal pattern is evident through the

Journal

European Journal of Plastic SurgerySpringer Journals

Published: Mar 1, 2012

References

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