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Case Report: Prune perineum syndrome: a rare case with an unfavourable outcome

Prune perineum syndrome (PPS) is a rare anomaly, with only two previous case reports, both dying in the perinatal period. We report the first case of PPS that reached childhood. The patient presented with a hypoplastic genitalia and bilateral cryptorchidism. There was no evidence of an anal orifice....

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Autores principales: Lopes, Roberto I., Dénes, Francisco T., Messi, Gustavo B., Machado, Marcos G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890296/
https://www.ncbi.nlm.nih.gov/pubmed/27303628
http://dx.doi.org/10.12688/f1000research.8246.2
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author Lopes, Roberto I.
Dénes, Francisco T.
Messi, Gustavo B.
Machado, Marcos G.
author_facet Lopes, Roberto I.
Dénes, Francisco T.
Messi, Gustavo B.
Machado, Marcos G.
author_sort Lopes, Roberto I.
collection PubMed
description Prune perineum syndrome (PPS) is a rare anomaly, with only two previous case reports, both dying in the perinatal period. We report the first case of PPS that reached childhood. The patient presented with a hypoplastic genitalia and bilateral cryptorchidism. There was no evidence of an anal orifice. A significant prune-like mass was observed, extending from the perineum to both gluteal regions and to a cephalic mid-line bony prominence, with a 1cm central orifice that discharged urine. MRI confirmed the previous findings and revealed a right crossed ectopic kidney, intestinal malrotation, a hypoplastic infrarenal inferior vena cava and a hypoplastic right iliac artery. Endoscopic evaluation through the orifice revealed a cavity lined by urothelial mucosa, with a small communication to the anterior urethra in its anterior wall. A staged reconstruction was planned, with a first-step urinary diversion through a continent abdominal reservoir associated to bilateral orchiopexy. He was discharged from the hospital three weeks later under intermittent catheterization. The next surgical step would be the resection of the perineal mass and its cavity associated to the removal of the prominent sacrococcygeal bones. Unfortunately, four months after the first surgery the patient developed an acute abdomen and was submitted to a laparotomy that revealed a necrotic ileal segment secondary to obstructive adherences. He developed severe malabsorption followed by septic shock, dying five weeks after the procedure. Due to the lack of literature, there is no consensus for the management of these cases. The wish of the family for a better quality of life and social acceptance, compelled us to perform a urinary diversion, to be followed by a plastic and orthopedic reconstruction. Despite the successful initial result, the patient developed a late abdominal obstruction that was misdiagnosed, precipitating his untimely death five months after the first procedure.
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spelling pubmed-48902962016-06-13 Case Report: Prune perineum syndrome: a rare case with an unfavourable outcome Lopes, Roberto I. Dénes, Francisco T. Messi, Gustavo B. Machado, Marcos G. F1000Res Case Report Prune perineum syndrome (PPS) is a rare anomaly, with only two previous case reports, both dying in the perinatal period. We report the first case of PPS that reached childhood. The patient presented with a hypoplastic genitalia and bilateral cryptorchidism. There was no evidence of an anal orifice. A significant prune-like mass was observed, extending from the perineum to both gluteal regions and to a cephalic mid-line bony prominence, with a 1cm central orifice that discharged urine. MRI confirmed the previous findings and revealed a right crossed ectopic kidney, intestinal malrotation, a hypoplastic infrarenal inferior vena cava and a hypoplastic right iliac artery. Endoscopic evaluation through the orifice revealed a cavity lined by urothelial mucosa, with a small communication to the anterior urethra in its anterior wall. A staged reconstruction was planned, with a first-step urinary diversion through a continent abdominal reservoir associated to bilateral orchiopexy. He was discharged from the hospital three weeks later under intermittent catheterization. The next surgical step would be the resection of the perineal mass and its cavity associated to the removal of the prominent sacrococcygeal bones. Unfortunately, four months after the first surgery the patient developed an acute abdomen and was submitted to a laparotomy that revealed a necrotic ileal segment secondary to obstructive adherences. He developed severe malabsorption followed by septic shock, dying five weeks after the procedure. Due to the lack of literature, there is no consensus for the management of these cases. The wish of the family for a better quality of life and social acceptance, compelled us to perform a urinary diversion, to be followed by a plastic and orthopedic reconstruction. Despite the successful initial result, the patient developed a late abdominal obstruction that was misdiagnosed, precipitating his untimely death five months after the first procedure. F1000Research 2016-06-10 /pmc/articles/PMC4890296/ /pubmed/27303628 http://dx.doi.org/10.12688/f1000research.8246.2 Text en Copyright: © 2016 Lopes RI et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Lopes, Roberto I.
Dénes, Francisco T.
Messi, Gustavo B.
Machado, Marcos G.
Case Report: Prune perineum syndrome: a rare case with an unfavourable outcome
title Case Report: Prune perineum syndrome: a rare case with an unfavourable outcome
title_full Case Report: Prune perineum syndrome: a rare case with an unfavourable outcome
title_fullStr Case Report: Prune perineum syndrome: a rare case with an unfavourable outcome
title_full_unstemmed Case Report: Prune perineum syndrome: a rare case with an unfavourable outcome
title_short Case Report: Prune perineum syndrome: a rare case with an unfavourable outcome
title_sort case report: prune perineum syndrome: a rare case with an unfavourable outcome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890296/
https://www.ncbi.nlm.nih.gov/pubmed/27303628
http://dx.doi.org/10.12688/f1000research.8246.2
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