Bilateral Xanthogranulomatous Pyelonephritis due to Staphylococcus Schleiferi: An Uncommon Presentation

Xanthogranulomatous pyelonephritis (XGP) describes a rare infectious disease with a destructive granulomatous process. The literature contains few cases of bilateral XGP and no cases due to Staphylococcus schleiferi; we diagnosed it with the advance at imaging and bacterial identification systems te...

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Autores principales: Aguilar Rivera, Leonardo René, Jiménez Castillo, Raúl Alberto, Zamora López, Miguel Ángel, Ortiz Meza, Itzel Araceli, Longoria Estrada, Ulises, Purón González, Emma, Rizo Topete, Lilia María
Formato: Artículo
Lenguaje:inglés
Publicado: 2021
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Acceso en línea:http://eprints.uanl.mx/24856/1/24856.pdf
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author Aguilar Rivera, Leonardo René
Jiménez Castillo, Raúl Alberto
Zamora López, Miguel Ángel
Ortiz Meza, Itzel Araceli
Longoria Estrada, Ulises
Purón González, Emma
Rizo Topete, Lilia María
author_facet Aguilar Rivera, Leonardo René
Jiménez Castillo, Raúl Alberto
Zamora López, Miguel Ángel
Ortiz Meza, Itzel Araceli
Longoria Estrada, Ulises
Purón González, Emma
Rizo Topete, Lilia María
author_sort Aguilar Rivera, Leonardo René
collection Repositorio Institucional
description Xanthogranulomatous pyelonephritis (XGP) describes a rare infectious disease with a destructive granulomatous process. The literature contains few cases of bilateral XGP and no cases due to Staphylococcus schleiferi; we diagnosed it with the advance at imaging and bacterial identification systems technology. This is a case of a 22-year-old female at our emergency department complaining of abdominal pain, nausea, emesis, dyspnea of 3 weeks. Medical history included Chronic Kidney Disease (CKD) treated with Peritoneal dialysis and history of recurrent urinary tract infection. On examination, we found signs of septic shock and suprapubic tenderness. No flank or renal mass found on examination. Tomography (CT) scan showed bilateral kidney enlargement with pyelocaliceal dilatation due to stones obstructing ureteral union; presence of gas on left kidney´s renal pelvis and an abscess in the posterior pararenal space. We diagnosed Bilateral XGP and emphysematous pyelitis, initiated boardspectrum antibiotic and perform urgent right nephrostomy and left nephrectomy. The urinary, blood and renal tissue culture identified pathogenic agents (Escherichia coli and Staphylococcus schleiferi) and antibiotic treatment was de-escalated. After two weeks of treatment, she recovered of an acute on chronic renal failure (ACRF) remaining with 24ml/min/1.73m2 of GFR (stage IV of CKD) and was discharged from hospital.
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spelling eprints-248562023-05-18T19:02:53Z http://eprints.uanl.mx/24856/ Bilateral Xanthogranulomatous Pyelonephritis due to Staphylococcus Schleiferi: An Uncommon Presentation Aguilar Rivera, Leonardo René Jiménez Castillo, Raúl Alberto Zamora López, Miguel Ángel Ortiz Meza, Itzel Araceli Longoria Estrada, Ulises Purón González, Emma Rizo Topete, Lilia María RC Medicina Interna, Psiquiatría, Neurología Xanthogranulomatous pyelonephritis (XGP) describes a rare infectious disease with a destructive granulomatous process. The literature contains few cases of bilateral XGP and no cases due to Staphylococcus schleiferi; we diagnosed it with the advance at imaging and bacterial identification systems technology. This is a case of a 22-year-old female at our emergency department complaining of abdominal pain, nausea, emesis, dyspnea of 3 weeks. Medical history included Chronic Kidney Disease (CKD) treated with Peritoneal dialysis and history of recurrent urinary tract infection. On examination, we found signs of septic shock and suprapubic tenderness. No flank or renal mass found on examination. Tomography (CT) scan showed bilateral kidney enlargement with pyelocaliceal dilatation due to stones obstructing ureteral union; presence of gas on left kidney´s renal pelvis and an abscess in the posterior pararenal space. We diagnosed Bilateral XGP and emphysematous pyelitis, initiated boardspectrum antibiotic and perform urgent right nephrostomy and left nephrectomy. The urinary, blood and renal tissue culture identified pathogenic agents (Escherichia coli and Staphylococcus schleiferi) and antibiotic treatment was de-escalated. After two weeks of treatment, she recovered of an acute on chronic renal failure (ACRF) remaining with 24ml/min/1.73m2 of GFR (stage IV of CKD) and was discharged from hospital. 2021 Article NonPeerReviewed text en cc_by_nc_nd http://eprints.uanl.mx/24856/1/24856.pdf http://eprints.uanl.mx/24856/1.haspreviewThumbnailVersion/24856.pdf Aguilar Rivera, Leonardo René y Jiménez Castillo, Raúl Alberto y Zamora López, Miguel Ángel y Ortiz Meza, Itzel Araceli y Longoria Estrada, Ulises y Purón González, Emma y Rizo Topete, Lilia María (2021) Bilateral Xanthogranulomatous Pyelonephritis due to Staphylococcus Schleiferi: An Uncommon Presentation. Arch Nephrol Urol, 4 (3). pp. 115-123.
spellingShingle RC Medicina Interna, Psiquiatría, Neurología
Aguilar Rivera, Leonardo René
Jiménez Castillo, Raúl Alberto
Zamora López, Miguel Ángel
Ortiz Meza, Itzel Araceli
Longoria Estrada, Ulises
Purón González, Emma
Rizo Topete, Lilia María
Bilateral Xanthogranulomatous Pyelonephritis due to Staphylococcus Schleiferi: An Uncommon Presentation
thumbnail https://rediab.uanl.mx/themes/sandal5/images/online.png
title Bilateral Xanthogranulomatous Pyelonephritis due to Staphylococcus Schleiferi: An Uncommon Presentation
title_full Bilateral Xanthogranulomatous Pyelonephritis due to Staphylococcus Schleiferi: An Uncommon Presentation
title_fullStr Bilateral Xanthogranulomatous Pyelonephritis due to Staphylococcus Schleiferi: An Uncommon Presentation
title_full_unstemmed Bilateral Xanthogranulomatous Pyelonephritis due to Staphylococcus Schleiferi: An Uncommon Presentation
title_short Bilateral Xanthogranulomatous Pyelonephritis due to Staphylococcus Schleiferi: An Uncommon Presentation
title_sort bilateral xanthogranulomatous pyelonephritis due to staphylococcus schleiferi an uncommon presentation
topic RC Medicina Interna, Psiquiatría, Neurología
url http://eprints.uanl.mx/24856/1/24856.pdf
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