Idiopathic retroperitoneal fibrosis (IRF) is an inflammatory and fibrosing
process that can be complicated by periureteral encasement, ureteral obstru
ction, and subsequent renal failure if left untreated. Unfortunately treatm
ent is often delayed die to the nonspecific nature of the presenting signs
and symptoms. Clinical, radiologic, and microscopic findings in IRF, if exa
mined independently are all nonspecific for its diagnosis. Rendering a diag
nosis of IRF by fine-needle aspiration (FNA) requires supportive clinical a
nd radiologic data and systematic evaluation of entities in the differentia
l diagnosis.
Herein we report 2 cases of IRF diagnosed by FNA with subsequent histologic
confirmation. Smears prepared from the aspirates revealed a combination of
inflammatory cells and fibrous tissue. The inflammatory: component was com
prised of a mixture of lymphocytes, plasma cells, and rare eosinophils and
mast cells. These 2 cases represent, to our knowledge, only the second repo
rt of IRF diagnosed by FNA. (C) 1999 Wiley-Liss, Inc.