BACKGROUND: Renal sarcoidosis exceptionally presents as a unilateral pyelic
pseudotumor as in this case where it was associated with granulomatous nep
hropathy.
CASE REPORT: A 33-year-old man had a two-year history of systemic sarcoidos
is with no renal involvement. He developed renal failure related to interst
itial granulomatous nephropathy associated with a pyelic localization leadi
ng to unilateral hydronephrosis. Urine drainage associated with corticoster
oid therapy provided a favorable course.
DISCUSSION: Renal involvement in sarcoidosis is usually the consequence of
hypercalcemia and hypercalciuria related to ectopic secretion of calcitriol
by the sarcoidosic granulomas, with urinary lithiasis and nephrocalcinosis
leading to renal failure and also granluomatous interstitial nephropathy.
Glomerulopathy or obstructive nephropathy are rarely reported. Intraluminal
localizations such as the pyelic lesion in our case are exceptional but mu
st be detected early since they respond to corticosteroid therapy.