Diagnosis of Takayasu arteritis is difficult because the clinical feat
ures are similar to those of other diseases, In early-phase Takayasu a
rteritis, computed tomography (CT) and magnetic resonance (MR) imaging
show thickening of the aortic wall, Late-phase Takayasu arteritis has
been classified into four types: classic pulseless disease (type I),
a mixed type (type II), the atypical coarctation type (type III), and
the dilated type (type TV), In late-phase Takayasu arteritis, angiogra
phy usually demonstrates luminal changes such as stenosis, occlusion,
or aneurysmal dilatation of the aorta and pulmonary artery and their b
ranches, However, absence of such luminal changes does not exclude the
possibility of early-phase Takayasu arteritis, Improvement in the cli
nical findings and subsidence of the active inflammatory process can b
e expected with early steroid treatment, Familiarity with the varied c
hest radiographic, angiographic, CT, and MR imaging features of Takaya
su arteritis will permit earlier diagnosis and treatment.