Pyonephrosis is a rare condition characterized by the destruction of renal parenchyma, which can lead to severe complications such as secondary peritonitis in cases of rupture. In this article, we report a rare case of acute peritonitis in a 12-year-old girl caused by ruptured pyonephrosis, occurring in a rural setting in Chad. The patient, with no prior medical history, was admitted for acute abdominal syndrome. She had experienced intermittent lumbar pain for six months, self-medicated without medical consultation. Radiological assessment revealed a markedly dilated right kidney with echogenic content suggestive of pyonephrosis overlying a renal calculus, along with abdominal fluid collection. A confirmatory CT scan could not be performed due to the unavailability of imaging facilities. Exploratory laparotomy revealed purulent intra-peritoneal fluid and a necrotic right kidney, necessitating nephrectomy. The patient recovered well postoperatively. Beyond its surgical relevance, this case highlights the urgent need for increased awareness regarding early medical consultation and improved access to advanced diagnostic tools in rural areas. To the best of our knowledge, this is the first reported case of pediatric peritonitis due to ruptured pyonephrosis managed entirely in a rural African setting.
| Published in | International Journal of Clinical Urology (Volume 9, Issue 2) |
| DOI | 10.11648/j.ijcu.20250902.24 |
| Page(s) | 192-195 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
| Copyright |
Copyright © The Author(s), 2025. Published by Science Publishing Group |
Urolithiasis, Pyonephrosis, Complication, Peritonitis, Health Policy
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APA Style
Nedjim, S. A., Younous, S., Vadandi, V., Fadoul, A., Kouldjim, A., et al. (2025). Peritonitis Due to Ruptured Pyonephrosis: First Case Report in a Child and Management in Rural Chad in Africa. International Journal of Clinical Urology, 9(2), 192-195. https://doi.org/10.11648/j.ijcu.20250902.24
ACS Style
Nedjim, S. A.; Younous, S.; Vadandi, V.; Fadoul, A.; Kouldjim, A., et al. Peritonitis Due to Ruptured Pyonephrosis: First Case Report in a Child and Management in Rural Chad in Africa. Int. J. Clin. Urol. 2025, 9(2), 192-195. doi: 10.11648/j.ijcu.20250902.24
@article{10.11648/j.ijcu.20250902.24,
author = {Saleh Abdelkerim Nedjim and Seid Younous and Valentin Vadandi and Achta Fadoul and Adoumadji Kouldjim and Moussa Kalli and Brahim Soukaya and Oumar Atti and Ndormadjita Allah-Siyangar and Mahamat Ali Mahamat and Rimtebaye Kimassoum and Choua Ouchemi},
title = {Peritonitis Due to Ruptured Pyonephrosis: First Case Report in a Child and Management in Rural Chad in Africa
},
journal = {International Journal of Clinical Urology},
volume = {9},
number = {2},
pages = {192-195},
doi = {10.11648/j.ijcu.20250902.24},
url = {https://doi.org/10.11648/j.ijcu.20250902.24},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijcu.20250902.24},
abstract = {Pyonephrosis is a rare condition characterized by the destruction of renal parenchyma, which can lead to severe complications such as secondary peritonitis in cases of rupture. In this article, we report a rare case of acute peritonitis in a 12-year-old girl caused by ruptured pyonephrosis, occurring in a rural setting in Chad. The patient, with no prior medical history, was admitted for acute abdominal syndrome. She had experienced intermittent lumbar pain for six months, self-medicated without medical consultation. Radiological assessment revealed a markedly dilated right kidney with echogenic content suggestive of pyonephrosis overlying a renal calculus, along with abdominal fluid collection. A confirmatory CT scan could not be performed due to the unavailability of imaging facilities. Exploratory laparotomy revealed purulent intra-peritoneal fluid and a necrotic right kidney, necessitating nephrectomy. The patient recovered well postoperatively. Beyond its surgical relevance, this case highlights the urgent need for increased awareness regarding early medical consultation and improved access to advanced diagnostic tools in rural areas. To the best of our knowledge, this is the first reported case of pediatric peritonitis due to ruptured pyonephrosis managed entirely in a rural African setting.
},
year = {2025}
}
TY - JOUR T1 - Peritonitis Due to Ruptured Pyonephrosis: First Case Report in a Child and Management in Rural Chad in Africa AU - Saleh Abdelkerim Nedjim AU - Seid Younous AU - Valentin Vadandi AU - Achta Fadoul AU - Adoumadji Kouldjim AU - Moussa Kalli AU - Brahim Soukaya AU - Oumar Atti AU - Ndormadjita Allah-Siyangar AU - Mahamat Ali Mahamat AU - Rimtebaye Kimassoum AU - Choua Ouchemi Y1 - 2025/11/07 PY - 2025 N1 - https://doi.org/10.11648/j.ijcu.20250902.24 DO - 10.11648/j.ijcu.20250902.24 T2 - International Journal of Clinical Urology JF - International Journal of Clinical Urology JO - International Journal of Clinical Urology SP - 192 EP - 195 PB - Science Publishing Group SN - 2640-1355 UR - https://doi.org/10.11648/j.ijcu.20250902.24 AB - Pyonephrosis is a rare condition characterized by the destruction of renal parenchyma, which can lead to severe complications such as secondary peritonitis in cases of rupture. In this article, we report a rare case of acute peritonitis in a 12-year-old girl caused by ruptured pyonephrosis, occurring in a rural setting in Chad. The patient, with no prior medical history, was admitted for acute abdominal syndrome. She had experienced intermittent lumbar pain for six months, self-medicated without medical consultation. Radiological assessment revealed a markedly dilated right kidney with echogenic content suggestive of pyonephrosis overlying a renal calculus, along with abdominal fluid collection. A confirmatory CT scan could not be performed due to the unavailability of imaging facilities. Exploratory laparotomy revealed purulent intra-peritoneal fluid and a necrotic right kidney, necessitating nephrectomy. The patient recovered well postoperatively. Beyond its surgical relevance, this case highlights the urgent need for increased awareness regarding early medical consultation and improved access to advanced diagnostic tools in rural areas. To the best of our knowledge, this is the first reported case of pediatric peritonitis due to ruptured pyonephrosis managed entirely in a rural African setting. VL - 9 IS - 2 ER -