Literature DB >> 26333104

Multimodal Imaging in Neurofibromatosis Type 1-associated Nerve Sheath Tumors.

J Salamon1, V F Mautner2, G Adam1, T Derlin3.   

Abstract

UNLABELLED: Neurofibromatosis type 1 (NF1) is a neurogenetic disorder. Individuals with NF1 may develop a variety of benign and malignant tumors of which peripheral nerve sheath tumors represent the most frequent entity. Plexiform neurofibromas may demonstrate a locally destructive growth pattern, may cause severe symptoms and may undergo malignant transformation into malignant peripheral nerve sheath tumors (MPNSTs). Whole-body magnetic resonance imaging (MRI) represents the reference standard for detection of soft tissue tumors in NF1. It allows for identification of individuals with plexiform neurofibromas, for assessment of local tumor extent, and for evaluation of whole-body tumor burden on T2-weighted imaging. Multiparametric MRI may provide a comprehensive characterization of different tissue properties of peripheral nerve sheath tumors, and may identify parameters associated with malignant transformation. Due to the absence of any radiation exposure, whole-body MRI may be used for serial follow-up of individuals with plexiform neurofibromas. (18)F-fluorodeoxyglucose positron-emission-tomography (FDG PET/CT) allows a highly sensitive and specific detection of MPNST, and should be used in case of potential malignant transformation of a peripheral nerve sheath tumor. PET/CT provides a sensitive whole-body tumor staging. The use of contrast-enhanced CT for diagnosis of peripheral nerve sheath tumors is limited to special indications. To obtain the most precise readings, optimized examination protocols and dedicated radiologists and nuclear medicine physicians familiar with the complex and variable morphologies of peripheral nerve sheath tumors are required. KEY POINTS: Individuals with NF1 may develop benign and malignant nerve sheath tumors. Whole-body MRI is the reference standard to identify nerve sheath tumors in NF1. MRI provides a comprehensive characterization of the growth pattern, growth dynamics and extent of nerve sheath tumors. (18)F-FDG PET/CT provides a sensitivity of 100% and a specificity of 77-95% for detection of malignant transformation. © Georg Thieme Verlag KG Stuttgart · New York.

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Year:  2015        PMID: 26333104     DOI: 10.1055/s-0035-1553505

Source DB:  PubMed          Journal:  Rofo        ISSN: 1438-9010


  13 in total

1.  Noninvasive Measurement of mTORC1 Signaling with 89Zr-Transferrin.

Authors:  Charles Truillet; John T Cunningham; Matthew F L Parker; Loc T Huynh; Crystal S Conn; Davide Ruggero; Jason S Lewis; Michael J Evans
Journal:  Clin Cancer Res       Date:  2016-12-22       Impact factor: 12.531

2.  Tumor segmentation of whole-body magnetic resonance imaging in neurofibromatosis type 1 patients: tumor burden correlates.

Authors:  Michael A Heffler; Lu Q Le; Yin Xi; Avneesh Chhabra
Journal:  Skeletal Radiol       Date:  2016-11-04       Impact factor: 2.199

3.  Surgical management of peripheral nerve sheath tumours in children, with special consideration of neurofibromatoses.

Authors:  Julian Zipfel; Meizer Al-Hariri; Isabel Gugel; Karin Haas-Lude; Alexander Grimm; Steven Warmann; Michael Krimmel; Victor-Felix Mautner; Marcos Tatagiba; Martin U Schuhmann
Journal:  Childs Nerv Syst       Date:  2020-06-06       Impact factor: 1.475

Review 4.  Emerging genotype-phenotype relationships in patients with large NF1 deletions.

Authors:  Hildegard Kehrer-Sawatzki; Victor-Felix Mautner; David N Cooper
Journal:  Hum Genet       Date:  2017-02-17       Impact factor: 4.132

5.  The effect of pregnancy on growth-dynamics of neurofibromas in Neurofibromatosis type 1.

Authors:  Lennart Well; Anna Jaeger; Hildegard Kehrer-Sawatzki; Said Farschtschi; Maxim Avanesov; Markus Sauer; Manuela Tavares de Sousa; Peter Bannas; Thorsten Derlin; Gerhard Adam; Victor F Mautner; Johannes M Salamon
Journal:  PLoS One       Date:  2020-04-28       Impact factor: 3.240

6.  Comparison of hybrid 18F-fluorodeoxyglucose positron emission tomography/magnetic resonance imaging and positron emission tomography/computed tomography for evaluation of peripheral nerve sheath tumors in patients with neurofibromatosis type 1.

Authors:  Roy A Raad; Shailee Lala; Jeffrey C Allen; James Babb; Carole Wind Mitchell; Ana M Franceschi; Kaleb Yohay; Kent P Friedman
Journal:  World J Nucl Med       Date:  2018 Oct-Dec

7.  How Effective Are Noninvasive Tests for Diagnosing Malignant Peripheral Nerve Sheath Tumors in Patients with Neurofibromatosis Type 1? Diagnosing MPNST in NF1 Patients.

Authors:  Maria Schwabe; Stanislav Spiridonov; Elizabeth L Yanik; Jack W Jennings; Travis Hillen; Maria Ponisio; Douglas J McDonald; Farrokh Dehdashti; Cara A Cipriano
Journal:  Sarcoma       Date:  2019-07-01

Review 8.  Peripheral nerve tumors of the hand: Clinical features, diagnosis, and treatment.

Authors:  Hai-Ying Zhou; Shuai Jiang; Fei-Xia Ma; Hui Lu
Journal:  World J Clin Cases       Date:  2020-11-06       Impact factor: 1.337

9.  Genotype-phenotype correlation in neurofibromatosis type-1: NF1 whole gene deletions lead to high tumor-burden and increased tumor-growth.

Authors:  Lennart Well; Kimberly Döbel; Lan Kluwe; Peter Bannas; Said Farschtschi; Gerhard Adam; Victor-Felix Mautner; Johannes Salamon
Journal:  PLoS Genet       Date:  2021-05-05       Impact factor: 5.917

Review 10.  The value of 18F-FDG PET/CT in patient with neurofibromatosis type 1: A case report and literature review.

Authors:  Jiazhong Ren; Guoren Yang; Jing Zhou; Zheng Fu
Journal:  Medicine (Baltimore)       Date:  2018-05       Impact factor: 1.889

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