A Successful Treatment of Encapsulating Peritoneal Sclerosis in an Adolescent Boy on Long-term Peritoneal Dialysis: A Case Report.
Encapsulating sclerosing peritonitis
Management
Peritoneal dialysis
Journal
Prague medical report
ISSN: 1214-6994
Titre abrégé: Prague Med Rep
Pays: Czech Republic
ID NLM: 101227436
Informations de publication
Date de publication:
2020
2020
Historique:
entrez:
3
12
2020
pubmed:
4
12
2020
medline:
29
1
2021
Statut:
ppublish
Résumé
Encapsulating peritoneal sclerosis (EPS) is a rare life-threatening complication associated with peritoneal dialysis (PD). EPS is characterized by progressive fibrosis and sclerosis of the peritoneum, with the formation of a membrane and tethering of loops of the small intestine resulting in intestinal obstruction. It is very rare in children. We present a case of a 16-year-old adolescent boy who developed EPS seven years after being placed on continuous ambulatory peritoneal dialysis (CAPD) complicated by several episodes of bacterial peritonitis. The diagnosis was based on clinical, radiological, intraoperative and histopathological findings. The patient was successfully treated with surgical enterolysis. During a 7-year follow-up, there have been no further episodes of small bowel obstruction documented. He still continues to be on regular hemodialysis and is awaiting a deceased donor kidney transplant. EPS is a long-term complication of peritoneal dialysis and is typically seen in adults. Rare cases may be seen in the pediatric population and require an appropriate surgical approach that is effective and lifesaving for these patients.
Identifiants
pubmed: 33270013
doi: 10.14712/23362936.2020.22
pii: pmr_2020121040254
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM