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2022, Volume 38, Number 2, Page(s) 122-132
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DOI: 10.5146/tjpath.2021.01561 |
Causes of Granulomatous Inflammation in Native and Allograft Kidneys: Case Series from A Single Center and A Review of the Literature |
Cihan HEYBELI1, Berna Demir YUKSEL21, Mehtat UNLU3, Mehmet Ası OKTAN4, Hayri Ustun ARDA5, Ozcan UZUN5, Filiz YILDIRIM5, Serkan YILDIZ6, Caner CAVDAR5, Aykut SIFIL5, Ali CELIK4, Sulen SARIOGLU3 |
1Division of Nephrology, Muş State Hospital, Muş, TURKEY 2Department of Internal Medicine, Dokuz Eylul University Hospital, Izmir, TURKEY 3Department of Pathology Dokuz Eylul University Hospital, Izmir, TURKEY 4Division of Nephrology, Baskent University Hospital, Izmir, TURKEY 5Dokuz Eylul University Hospital, Izmir, TURKEY, 6Medicana Hospital, Izmir, TURKEY |
Keywords:
Granuloma, Renal biopsy, Pathology, Renal |
Objective: Granulomatous interstitial nephritis is a rare finding, and etiology differs by geography. We aimed to investigate the distribution of
causes of granuloma/granulomata in the kidney and renal survival of these patients in a tertiary care hospital in Western Turkey.
Material and Method: Medical records of adults who underwent a kidney biopsy procedure in our institution between January 2000 and June
2019 were reviewed. Pathology reports were searched for biopsies where a granuloma was identified.
Results: Nineteen of 1121 (1.7%) kidney biopsies included granuloma, 17 in native kidneys, and 2 in transplants. The majority of indications
for native kidney biopsy was a rise in serum creatinine. Etiologies of granuloma included the following: pauci-immune vasculitis (n=11, 64.7%),
tuberculosis (n=2, 11.8%), drug-induced (n=2, 11.8%), tubulointerstitial nephritis/uveitis (TINU) syndrome (n=1, 5.9%), and systemic-lupus
erythematosus (n=1, 5.9%). Despite treatment, 6 of 11 (54.5%) patients with vasculitis developed end-stage kidney disease (ESKD) during the
median follow-up of 16 months. Both of the patients with tuberculosis, and the patient with TINU syndrome developed ESKD months after
the kidney biopsy, despite appropriate therapies. The only case with drug-induced granuloma and both cases with allograft kidney granuloma
responded well to glucocorticoids, achieving a complete renal recovery.
Conclusion: The majority of our series had granuloma in the kidney secondary to vasculitis and renal outcomes appear considerably unfavorable
despite treatment, probably related to the primary diagnosis. Multicenter studies are needed to better determine the etiology and outcome of
each granuloma etiology at different geographic locations.
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