Purpose: To assess the computed tomographic (CT) findings of intrathor
acic involvement in multicentric Castleman disease. Materials and meth
ods: The study comprised 12 patients with lymph node biopsy-proved Cas
tleman disease and multicentric involvement. The patients were aged 23
-58 years (mean age, 42.9 years; five men, seven women). Seven patient
s underwent open lung biopsy (n = 3) or transbronchial lung biopsy (n
= 4), which demonstrated lymphocytic interstitial pneumonitis. Results
: All patients had systemic symptoms, polyclonal hypergammaglobulinemi
a, and bilateral hilar and mediastinal lymph node enlargement. The nod
es a showed mild to moderate enhancement after intravenous administrat
ion of contrast material. At thin-section CT, all 12 patients showed p
oorly defined centrilobular nodules. Thin-walled cysts were present in
10 patients, thickening of the bronchovascular bundles in 10, and int
erlobular septal thickening in nine. Less common findings were subpleu
ral nodules, ground-glass attenuation, air-space consolidation, and br
onchiectasis. Conclusion: Multicentric Castleman disease is characteri
zed by the presence of systemic symptoms, bilateral hilar and mediasti
nal lymphadenopathy, and centrilobular nodular opacities. The pulmonar
y parenchymal findings are due to the associated lymphocytic interstit
ial pneumonitis.