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1 From the Department of Radiologic Pathology, Armed Forces Institute of Pathology, 6825 16th Street NW, Bldg 54, Room M-133A, Washington, DC 20306 (M.D.M., W.S.S., S.E.S.); Departments of Radiology and Nuclear Medicine (M.D.M., W.S.S.) and Surgery (H.T.T.), Uniformed Services University of the Health Sciences, Bethesda, Md; Department of Radiology, University of Maryland School of Medicine, Baltimore (M.D.M., S.E.S.); Department of Surgery, Orthopedic Service, Walter Reed Army Medical Center, Washington, DC (H.T.T.); Department of Radiology, St Mary's Hospital, Richmond, Va (M.J.K.). Received April 8, 1999; revision requested April 26 and received May 28; accepted June 1. Presented as a scientific exhibit at the 1995 RSNA scientific assembly. Address reprint requests to M.D.M.
Numerous neurogenic tumors can affect the musculoskeletal system, including traumatic neuroma, Morton neuroma, neural fibrolipoma, nerve sheath ganglion, neurilemoma, neurofibroma, and malignant peripheral nerve sheath tumors (PNSTs). The diagnosis of neurogenic tumors can be suggested from their imaging appearances, including lesion shape and intrinsic imaging characteristics. It is also important to establish lesion location along a typical nerve distribution (eg, plantar digital nerve in Morton neuroma, median nerve in neural fibrolipoma, large nerve trunk in benign and malignant PNSTs). Traumatic and Morton neuromas are commonly related to an amputation stump or are located in the intermetatarsal space, respectively. Neural fibrolipomas show fat interspersed between nerve fascicles and are often associated with macrodactyly. Nerve sheath ganglion has a cystic appearance and commonly occurs about the knee. Radiologic characteristics of neurilemoma, neurofibroma, and malignant PNST at computed tomography (CT), ultrasonography, and magnetic resonance imaging include fusiform shape, identification of entering and exiting nerve, low attenuation at CT, target sign, fascicular sign, split-fat sign, and associated muscle atrophy. Although differentiation of neurilemoma from neurofibroma and of benign from malignant PNST is problematic, recognition of the radiologic appearances of neurogenic tumors often allows prospective diagnosis and improves clinical management of patients.
Index Terms: Nervous system, neoplasms, 4.315, 4.325, 4.364 Neurofibromatosis, 4.1444, 4.1831 Neuroma, 4.315, 4.364
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