Objective.-A clinicopathologic review of splenic involvement in Wegene
r's granulomatosis. Design.-A retrospective case review, spanning a 10
-year period, identified five patients with Wegener's granulomatosis a
nd splenic involvement. Setting.-A large teaching hospital and outpati
ent clinics. Interventions.-Cytotoxic therapy (cyclophosphamide and co
rticosteroids), mechanical ventilation in respiratory failure, renal h
emodialysis in renal failure, and general supportive care. Results.-Ne
crotizing granulomatous inflammation and vasculitis with fibrinoid nec
rosis were found in the spleen in one antemortem case. At autopsy, two
cases demonstrated extensive infarction; microscopic examination reve
aled parenchymal coagulative necrosis, microcalcification, and vascula
r thrombosis, but no evidence of vasculitis. Two other cases showed no
nspecific changes of diffuse hyalinization of blood vessels, vascular
congestion, and hemosiderin deposition. Conclusions.-Splenic involveme
nt in Wegener's granulomatosis is rarely diagnosed during life, occurs
more frequently than once thought, and can occasionally lead to consi
derable morbidity.