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Malignant Peripheral Nerve Sheath Tumors: Use of 18FDG-PET/CT

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Tumors of the Central Nervous system, Volume 3

Part of the book series: Tumors of the Central Nervous System ((TCNS,volume 3))

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Abstract

Malignant Peripheral Nerve Sheath Tumors (MPNST) are rare but lethal lesions. They are more often found in patients with the cancer pre-disposition syndrome, Neurofibromatosis 1 (NF1). NF1 patients harbor many peripheral nerve tumors, the majority of which are benign. Early detection of these benign plexiform neurofibromas (PNf), which may have transformed to a MPNST, is of paramount importance in the long term management and outcome of these patients. However, surveillance of these PNfs is cumbersome as the clinical and radiological features suggestive of malignant transformation are often inaccurate and surgery can lead to significant morbidity. One imaging strategy that is of promise is to take advantage of the fact that malignant tumors inherently are actively proliferating with accompanying increased and altered glucose metabolism, compared to benign lesions. This is the theoretical premise for using 18-Fluorodeoxyglucose (18-FDG)-Positron Emission Tomography (PET) imaging to help diagnose and guide management of MPNSTs.

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Correspondence to Abhijit Guha .

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le Roux, A.A., Guha, A. (2011). Malignant Peripheral Nerve Sheath Tumors: Use of 18FDG-PET/CT. In: Hayat, M. (eds) Tumors of the Central Nervous system, Volume 3. Tumors of the Central Nervous System, vol 3. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-1399-4_13

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  • DOI: https://doi.org/10.1007/978-94-007-1399-4_13

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