Numerous neurogenic tumors can affect the musculoskeletal system, including
traumatic neuroma, Morton neuroma, neural fibrolipoma, nerve sheath gangli
on, neurilemoma, neurofibroma, and malignant peripheral nerve sheath tumors
(PNSTs), The diagnosis of neurogenic tumors can be suggested from their im
aging appearances, including lesion shape and intrinsic imaging characteris
tics. It is also important to establish lesion location along a typical ner
ve distribution (eg:, plantar digital nerve in Morton neuroma, median nerve
in neural fibrolipoma, large nerve trunk in benign and malignant PNSTs), T
raumatic and Morton neuromas are commonly related to an amputation stump or
are located in the intermetatarsal space, respectively. Neural fibrolipoma
s show fat interspersed between nerve fascicles and are often associated wi
th macrodactyly. Nerve sheath ganglion has a cystic appearance and commonly
occurs about the knee. Radiologic characteristics of neurilemoma, neurofib
roma, and malignant PNST at computed tomography (CT), ultrasonography, and
magnetic imaging include fusiform shape, identification of entering and exi
ting nerve, low attenuation at CT, target sign, fascicular sign, split-fat
sign, and associated muscle atrophy. Although differentiation of neurilemom
a from neurofibroma of beni:pn from malignant PNST is problematic, recognit
ion of the radiologic appearances of neurogenic tumors often allows prospec
tive diagnosis and improves clinical management of patients.