Acute Kidney Failure in a Young African American Male

Retroperitoneal fibrosis (RPF) is a condition characterized by chronic inflammatory and fibrotic changes in the retroperitoneum that can lead to serious complications including kidney failure, mesenteric and limb ischemia, and deep venous thrombosis among others. Affected individuals may present wit...

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Main Authors: Thuan V. Nguyen, Nada M. Bader, Harpreet Sidhu, Caprice Cadacio, Susana M. Mendoza, Phuong Thu T. Pham, Phuong Chi T. Pham
Format: Article
Language:English
Published: Wiley 2019-01-01
Series:Case Reports in Nephrology
Online Access:http://dx.doi.org/10.1155/2019/2591560
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author Thuan V. Nguyen
Nada M. Bader
Harpreet Sidhu
Caprice Cadacio
Susana M. Mendoza
Phuong Thu T. Pham
Phuong Chi T. Pham
author_facet Thuan V. Nguyen
Nada M. Bader
Harpreet Sidhu
Caprice Cadacio
Susana M. Mendoza
Phuong Thu T. Pham
Phuong Chi T. Pham
author_sort Thuan V. Nguyen
collection DOAJ
description Retroperitoneal fibrosis (RPF) is a condition characterized by chronic inflammatory and fibrotic changes in the retroperitoneum that can lead to serious complications including kidney failure, mesenteric and limb ischemia, and deep venous thrombosis among others. Affected individuals may present with nonspecific symptomology that would require a high clinical index of suspicion for prompt diagnosis. We herein discuss a case of a young African-American man with recurrent deep venous thrombosis who presents with a 4-week history of constant aching pain of abdomen and back and kidney failure. Initial noncontrast computed tomogram (CT) only revealed mild bilateral hydroureteronephrosis with inflammatory changes but without obvious mass or lymphadenopathy. At the insistence of the renal consulting team to rule out RPF, a CT-urogram was performed which revealed an infiltrative mass encasing the aorta, inferior vena cava, and common iliac vessels. Laparoscopic biopsy revealed dense fibroadipose tissue, lymphocytic aggregates, focal scattered IgG4-positive plasma cells, and fibrin deposition. Patient underwent bilateral nephrostomy placement and empirical corticosteroid therapy with resolution of kidney failure. Our case illustrates a classic presentation of RPF with relatively benign findings on noncontrast CT that could have been missed if clinicians did not keep a high index of suspicion for the condition.
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spelling doaj-art-c4a5c331b422422aa62b79cd1edbfd8e2025-08-20T02:18:46ZengWileyCase Reports in Nephrology2090-66412090-665X2019-01-01201910.1155/2019/25915602591560Acute Kidney Failure in a Young African American MaleThuan V. Nguyen0Nada M. Bader1Harpreet Sidhu2Caprice Cadacio3Susana M. Mendoza4Phuong Thu T. Pham5Phuong Chi T. Pham6Olive View-UCLA Medical Center, Division of Nephrology and Hypertension, Los Angeles, CA 91342, USAOlive View-UCLA Medical Center, Division of Nephrology and Hypertension, Los Angeles, CA 91342, USAOlive View-UCLA Medical Center, Division of Nephrology and Hypertension, Los Angeles, CA 91342, USAOlive View-UCLA Medical Center, Division of Nephrology and Hypertension, Los Angeles, CA 91342, USAOlive View-UCLA Medical Center, Division of Nephrology and Hypertension, Los Angeles, CA 91342, USADavid Geffen School of Medicine at UCLA, Kidney Transplant, Los Angeles, CA 90095, USAOlive View-UCLA Medical Center, Division of Nephrology and Hypertension, Los Angeles, CA 91342, USARetroperitoneal fibrosis (RPF) is a condition characterized by chronic inflammatory and fibrotic changes in the retroperitoneum that can lead to serious complications including kidney failure, mesenteric and limb ischemia, and deep venous thrombosis among others. Affected individuals may present with nonspecific symptomology that would require a high clinical index of suspicion for prompt diagnosis. We herein discuss a case of a young African-American man with recurrent deep venous thrombosis who presents with a 4-week history of constant aching pain of abdomen and back and kidney failure. Initial noncontrast computed tomogram (CT) only revealed mild bilateral hydroureteronephrosis with inflammatory changes but without obvious mass or lymphadenopathy. At the insistence of the renal consulting team to rule out RPF, a CT-urogram was performed which revealed an infiltrative mass encasing the aorta, inferior vena cava, and common iliac vessels. Laparoscopic biopsy revealed dense fibroadipose tissue, lymphocytic aggregates, focal scattered IgG4-positive plasma cells, and fibrin deposition. Patient underwent bilateral nephrostomy placement and empirical corticosteroid therapy with resolution of kidney failure. Our case illustrates a classic presentation of RPF with relatively benign findings on noncontrast CT that could have been missed if clinicians did not keep a high index of suspicion for the condition.http://dx.doi.org/10.1155/2019/2591560
spellingShingle Thuan V. Nguyen
Nada M. Bader
Harpreet Sidhu
Caprice Cadacio
Susana M. Mendoza
Phuong Thu T. Pham
Phuong Chi T. Pham
Acute Kidney Failure in a Young African American Male
Case Reports in Nephrology
title Acute Kidney Failure in a Young African American Male
title_full Acute Kidney Failure in a Young African American Male
title_fullStr Acute Kidney Failure in a Young African American Male
title_full_unstemmed Acute Kidney Failure in a Young African American Male
title_short Acute Kidney Failure in a Young African American Male
title_sort acute kidney failure in a young african american male
url http://dx.doi.org/10.1155/2019/2591560
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