Current status and recommendations for imaging in neurofibromatosis type 1, neurofibromatosis type 2, and schwannomatosis.

Humans Magnetic Resonance Imaging / methods Magnetic Resonance Spectroscopy / methods Neurilemmoma / diagnostic imaging Neurofibromatoses / diagnostic imaging Neurofibromatosis 1 / diagnostic imaging Neurofibromatosis 2 / diagnostic imaging Positron-Emission Tomography / methods Skin Neoplasms / diagnostic imaging
Apparent diffusion coefficient (ADC) values Diffusion-weighted imaging (DWI) Imaging biomarkers Magnetic resonance imaging (MRI) Malignant peripheral nerve sheath tumor (MPNST) Neurofibromatosis type 1 (NF1) Neurofibromatosis type 2 (NF2) Schwannomatosis (SWN)

Journal

Skeletal radiology
ISSN: 1432-2161
Titre abrégé: Skeletal Radiol
Pays: Germany
ID NLM: 7701953

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 07 06 2019
accepted: 24 07 2019
revised: 23 07 2019
pubmed: 10 8 2019
medline: 1 8 2020
entrez: 10 8 2019
Statut: ppublish

Résumé

Neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2), and schwannomatosis (SWN) are three clinically distinct tumor predisposition syndromes with a shared tendency to develop peripheral and central nervous system neoplasms. Disease expression and complications of NF1, NF2, and SWN are highly variable, necessitating a multidisciplinary approach to care in order to optimize outcomes. This review will discuss the imaging appearance of NF1, NF2, and SWN and highlight the important role that imaging plays in informing management decisions in people with tumors associated with these syndromes. Recent technological advances, including the role of both whole-body and localized imaging strategies, routine anatomic and advanced magnetic resonance (MR) imaging sequences such as diffusion-weighted imaging (DWI) with quantitative apparent diffusion coefficient (ADC) mapping, and metabolic imaging techniques (MR spectroscopy and positron emission testing) are discussed in the context of the diagnosis and management of people with NF1, NF2, and SWN based on the most up-to-date clinical imaging studies.

Identifiants

DOI: 10.1007/s00256-019-03290-1 PMID: 31396668
pubmed: 31396668
doi: 10.1007/s00256-019-03290-1
pii: 10.1007/s00256-019-03290-1
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

199-219

Commentaires et corrections

Type : CommentIn

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Auteurs

Shivani Ahlawat (S)

The Russell H. Morgan Department of Radiology & Radiological Science, The Johns Hopkins University School of Medicine, 601 North Caroline Street, JHOC 3rd Floor, Baltimore, MD, 21287, USA. sahlawa1@jhmi.edu.
ORCID: 0000-0003-4437-5237

Jaishri O Blakeley (JO)

Department of Neurology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Department of Neurosurgery, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Shannon Langmead (S)

Department of Neurology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Allan J Belzberg (AJ)

Department of Neurosurgery, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Laura M Fayad (LM)

The Russell H. Morgan Department of Radiology & Radiological Science, The Johns Hopkins University School of Medicine, 601 North Caroline Street, JHOC 3rd Floor, Baltimore, MD, 21287, USA.
Department of Orthopaedic Surgery, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.

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questionsmedicales.fr › Malformations et maladies congénitales, héréditaires et néonatales › Maladies génétiques congénitales › Syndromes néoplasiques héréditaires › Neurofibromatoses › Current status and recommendations for imaging...
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questionsmedicales.fr › Malformations et maladies congénitales, héréditaires et néonatales › Maladies génétiques congénitales › Syndromes néoplasiques héréditaires › Neurofibromatoses › Neurofibromatose de type 2 › Current status and recommendations for imaging...
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