Neurilemomas and neurofibromas appear as round soft tissue masses at CT. Va
riable enhancement with either homogeneity or heterogeneity is seen in neur
ilemomas. Attenuation of the tumors on enhanced CT depends on histology: th
e extent of Antoni A or B tissue and the amount of myxoid or cystic degener
ation or hemorrhage. Neurofibromas are usually homogeneous low attenuation
lesions on unenhanced CT. They show homogeneous enhancement or early centra
l blush on enhanced scan. The extent of enhancement depends on the proporti
ons of tumor components: nerve sheath cells, collagen bundles, and areas of
myxoid degeneration. Malignant nerve sheath tumors show variable attenuati
on. Bony destruction, pleural effusion, and metastatic pulmonary nodules ma
y also occur. Ganglioneuromas appear as oblong homogeneous low attenuation
lesions on both enhanced and unenhanced CT. This low attenuation is due to
their pathologic components, with an abundant amount of myxoid matrices and
a relatively small amount of ganglion cells. Neuroblastomas appear as aggr
essive soft tissue lesions with calcification. Ganglioneuroblastomas may ap
pear with features in between those of ganglioneuromas and neuroblastomas.
The typical location of the posterior mediastinum or the aortopulmonary win
dow and high enhancement with administration of contrast medium at CT sugge
st the diagnosis of paragangliomas.