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Positron emission tomography and magnetic resonance imaging in primary central nervous system lymphoma—a narrative review

This review addresses the challenges of primary central nervous system (CNS) lymphoma diagnosis, assessment of treatment response, and detection of recurrence. Primary CNS lymphoma is a rare form of extra-nodal non-Hodgkin lymphoma that can involve brain, spinal cord, leptomeninges, and eyes. Primar...

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Autores principales: Krebs, Simone, Barasch, Julia G., Young, Robert J., Grommes, Christian, Schöder, Heiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248935/
https://www.ncbi.nlm.nih.gov/pubmed/34223561
http://dx.doi.org/10.21037/aol-20-52
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author Krebs, Simone
Barasch, Julia G.
Young, Robert J.
Grommes, Christian
Schöder, Heiko
author_facet Krebs, Simone
Barasch, Julia G.
Young, Robert J.
Grommes, Christian
Schöder, Heiko
author_sort Krebs, Simone
collection PubMed
description This review addresses the challenges of primary central nervous system (CNS) lymphoma diagnosis, assessment of treatment response, and detection of recurrence. Primary CNS lymphoma is a rare form of extra-nodal non-Hodgkin lymphoma that can involve brain, spinal cord, leptomeninges, and eyes. Primary CNS lymphoma lesions are most commonly confined to the white matter or deep cerebral structures such as basal ganglia and deep periventricular regions. Contrast-enhanced magnetic resonance imaging (MRI) is the standard diagnostic modality employed by neuro-oncologists. MRI often shows common morphological features such as a single or multiple uniformly well-enhancing lesions without necrosis but with moderate surrounding edema. Other brain tumors or inflammatory processes can show similar radiological patterns, making differential diagnosis difficult. [18F]-fluorodeoxyglucose (FDG) positron emission tomography (PET) has selected utility in cerebral lymphoma, especially in diagnosis. Primary CNS lymphoma can sometimes present with atypical findings on MRI and FDG PET, such as disseminated disease, non-enhancing or ring-like enhancing lesions. The complementary strengths of PET and MRI have led to the development of combined PET-MR systems, which in some cases may improve lesion characterization and detection. By highlighting active developments in this field, including advanced MRI sequences, novel radiotracers, and potential imaging biomarkers, we aim to spur interest in sophisticated imaging approaches.
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spelling pubmed-82489352021-07-01 Positron emission tomography and magnetic resonance imaging in primary central nervous system lymphoma—a narrative review Krebs, Simone Barasch, Julia G. Young, Robert J. Grommes, Christian Schöder, Heiko Ann Lymphoma Article This review addresses the challenges of primary central nervous system (CNS) lymphoma diagnosis, assessment of treatment response, and detection of recurrence. Primary CNS lymphoma is a rare form of extra-nodal non-Hodgkin lymphoma that can involve brain, spinal cord, leptomeninges, and eyes. Primary CNS lymphoma lesions are most commonly confined to the white matter or deep cerebral structures such as basal ganglia and deep periventricular regions. Contrast-enhanced magnetic resonance imaging (MRI) is the standard diagnostic modality employed by neuro-oncologists. MRI often shows common morphological features such as a single or multiple uniformly well-enhancing lesions without necrosis but with moderate surrounding edema. Other brain tumors or inflammatory processes can show similar radiological patterns, making differential diagnosis difficult. [18F]-fluorodeoxyglucose (FDG) positron emission tomography (PET) has selected utility in cerebral lymphoma, especially in diagnosis. Primary CNS lymphoma can sometimes present with atypical findings on MRI and FDG PET, such as disseminated disease, non-enhancing or ring-like enhancing lesions. The complementary strengths of PET and MRI have led to the development of combined PET-MR systems, which in some cases may improve lesion characterization and detection. By highlighting active developments in this field, including advanced MRI sequences, novel radiotracers, and potential imaging biomarkers, we aim to spur interest in sophisticated imaging approaches. 2021-06-30 2021-06 /pmc/articles/PMC8248935/ /pubmed/34223561 http://dx.doi.org/10.21037/aol-20-52 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-Non-Commercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the noncommercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Article
Krebs, Simone
Barasch, Julia G.
Young, Robert J.
Grommes, Christian
Schöder, Heiko
Positron emission tomography and magnetic resonance imaging in primary central nervous system lymphoma—a narrative review
title Positron emission tomography and magnetic resonance imaging in primary central nervous system lymphoma—a narrative review
title_full Positron emission tomography and magnetic resonance imaging in primary central nervous system lymphoma—a narrative review
title_fullStr Positron emission tomography and magnetic resonance imaging in primary central nervous system lymphoma—a narrative review
title_full_unstemmed Positron emission tomography and magnetic resonance imaging in primary central nervous system lymphoma—a narrative review
title_short Positron emission tomography and magnetic resonance imaging in primary central nervous system lymphoma—a narrative review
title_sort positron emission tomography and magnetic resonance imaging in primary central nervous system lymphoma—a narrative review
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248935/
https://www.ncbi.nlm.nih.gov/pubmed/34223561
http://dx.doi.org/10.21037/aol-20-52
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