| Literature DB >> 30699454 |
Alberto Stefano Tagliafico1,2, Amanda Isaac3,4, Bianca Bignotti1, Federica Rossi1, Federico Zaottini1, Carlo Martinoli1,2.
Abstract
Nerve 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. Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.Entities:
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Year: 2019 PMID: 30699454 DOI: 10.1055/s-0038-1676290
Source DB: PubMed Journal: Semin Musculoskelet Radiol ISSN: 1089-7860 Impact factor: 1.777