Nerve Tumors: What the MSK Radiologist Should Know

Author:

Isaac Amanda12,Bignotti Bianca3,Rossi Federica3,Zaottini Federico3,Martinoli Carlo34,Tagliafico Alberto34

Affiliation:

1. Guy's and St Thomas' Hospitals NHS Foundation Trust, London, United Kingdom

2. King's College London, London, United Kingdom

3. Department of Health Sciences (DISSAL), University of Genoa, Genova, Italy

4. IRCCS Ospedale Policlinico San Martino, Genova, Italy

Abstract

AbstractNerve tumors are rare and heterogeneous soft tissue tumors arising from a peripheral nerve or showing nerve sheath differentiation. In a radiologic setting it is necessary to recognize soft tissue lesions that are of neural origin, their association with a peripheral nerve, and whether they are a true tumor or a so-called pseudotumor such as a neuroma, fibrolipoma, or peripheral nerve sheath ganglion. Ultrasound (US) and magnetic resonance imaging are the best modalities to characterize these lesions. US can be used to guide biopsy in difficult and uncertain cases when the lesion is either indeterminate or possibly malignant. At present, no single imaging feature or reproducible criteria, or a combination, can differentiate reliably between a neurofibroma and a schwannoma or discriminate with certainty between benign and malignant neurogenic tumors. Adequate imaging and consultation with a nerve tumors/sarcoma unit is advised.

Publisher

Georg Thieme Verlag KG

Subject

Radiology Nuclear Medicine and imaging,Orthopedics and Sports Medicine

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