Utility of FDG-PETCT and magnetic resonance spectroscopy in differentiating between cerebral lymphoma and non-malignant CNS lesions in HIV-infected patients

Abstract Background and purpose In HIV infected patients, MRI cannot reliably differentiate between central nervous system (CNS) lymphoma and non-malignant CNS lesions, particularly cerebral toxoplasmosis (CTOX). This study prospectively investigates the utility of FDG PET-CT and magnetic resonance...

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Veröffentlicht in:European journal of radiology 2013-08, Vol.82 (8), p.e374-e379
Hauptverfasser: Westwood, Thomas D, Hogan, Celia, Julyan, Peter J, Coutts, Glyn, Bonington, Suzie, Carrington, Bernadette, Taylor, Ben, Khoo, Saye, Bonington, Alec
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container_end_page e379
container_issue 8
container_start_page e374
container_title European journal of radiology
container_volume 82
creator Westwood, Thomas D
Hogan, Celia
Julyan, Peter J
Coutts, Glyn
Bonington, Suzie
Carrington, Bernadette
Taylor, Ben
Khoo, Saye
Bonington, Alec
description Abstract Background and purpose In HIV infected patients, MRI cannot reliably differentiate between central nervous system (CNS) lymphoma and non-malignant CNS lesions, particularly cerebral toxoplasmosis (CTOX). This study prospectively investigates the utility of FDG PET-CT and magnetic resonance spectroscopy (MRS) in discriminating CNS lymphoma from non-malignant CNS lesions in HIV infected patients, and assesses the ability of FDG PET-CT to guide the use of early brain biopsy. Methods 10 HIV patients with neurological symptoms and contrast enhancing lesions on MRI were commenced on anti-toxoplasmosis therapy before undergoing FDG PET-CT and MRS. Brain biopsies were sought in those with FDG PET-CT suggestive of CNS lymphoma, and in those with a negative FDG PET-CT scan who failed to respond to therapy. Final diagnosis was based on histology or treatment response. Results Two patients were confirmed to have CNS lymphoma and FDG PET-CT was consistent with this diagnosis in both. Six patients had cerebral toxoplasmosis in all of whom FDG PET-CT was consistent with non-malignant disease. One patient had progressive multifocal leukoencephalopathy (PML), FDG PET-CT was equivocal. One patient had a haemorrhagic brain metastasis and FDG PET-CT wrongly suggested non-malignant disease. MRS was performed successfully in eight subjects: three results were suggestive of CNS lymphoma (one true positive, two false positive), four suggested CTOX (two false negative, two true negative), one scan was equivocal. Conclusion FDG PET-CT correctly identified all cases of CNS lymphoma and CTOX, supporting its use in this situation. MRS was unhelpful in our cohort.
doi_str_mv 10.1016/j.ejrad.2013.03.008
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This study prospectively investigates the utility of FDG PET-CT and magnetic resonance spectroscopy (MRS) in discriminating CNS lymphoma from non-malignant CNS lesions in HIV infected patients, and assesses the ability of FDG PET-CT to guide the use of early brain biopsy. Methods 10 HIV patients with neurological symptoms and contrast enhancing lesions on MRI were commenced on anti-toxoplasmosis therapy before undergoing FDG PET-CT and MRS. Brain biopsies were sought in those with FDG PET-CT suggestive of CNS lymphoma, and in those with a negative FDG PET-CT scan who failed to respond to therapy. Final diagnosis was based on histology or treatment response. Results Two patients were confirmed to have CNS lymphoma and FDG PET-CT was consistent with this diagnosis in both. Six patients had cerebral toxoplasmosis in all of whom FDG PET-CT was consistent with non-malignant disease. One patient had progressive multifocal leukoencephalopathy (PML), FDG PET-CT was equivocal. One patient had a haemorrhagic brain metastasis and FDG PET-CT wrongly suggested non-malignant disease. MRS was performed successfully in eight subjects: three results were suggestive of CNS lymphoma (one true positive, two false positive), four suggested CTOX (two false negative, two true negative), one scan was equivocal. Conclusion FDG PET-CT correctly identified all cases of CNS lymphoma and CTOX, supporting its use in this situation. MRS was unhelpful in our cohort.</description><identifier>ISSN: 0720-048X</identifier><identifier>EISSN: 1872-7727</identifier><identifier>DOI: 10.1016/j.ejrad.2013.03.008</identifier><identifier>PMID: 23578921</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Adult ; Biomarkers - analysis ; Brain Diseases - diagnosis ; Brain Diseases - metabolism ; Central nervous system ; Diagnosis, Differential ; Female ; Fluorodeoxyglucose F18 ; HIV ; HIV Infections - diagnosis ; HIV Infections - metabolism ; Humans ; Lymphoma ; Lymphoma, AIDS-Related - diagnosis ; Lymphoma, AIDS-Related - metabolism ; Magnetic resonance spectroscopy ; Magnetic Resonance Spectroscopy - methods ; Male ; Multimodal Imaging - methods ; Positron emission tomography and computed tomography ; Positron-Emission Tomography - methods ; Radiology ; Radiopharmaceuticals ; Reproducibility of Results ; Sensitivity and Specificity ; Tomography, X-Ray Computed - methods ; United Kingdom</subject><ispartof>European journal of radiology, 2013-08, Vol.82 (8), p.e374-e379</ispartof><rights>2013</rights><rights>Crown Copyright © 2013. Published by Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c480t-d65ef9bb23ad476422ee9f2c7b8c7cc7192e75ecd3b2d75de7ad4bda6c4ff1f13</citedby><cites>FETCH-LOGICAL-c480t-d65ef9bb23ad476422ee9f2c7b8c7cc7192e75ecd3b2d75de7ad4bda6c4ff1f13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0720048X1300137X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23578921$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Westwood, Thomas D</creatorcontrib><creatorcontrib>Hogan, Celia</creatorcontrib><creatorcontrib>Julyan, Peter J</creatorcontrib><creatorcontrib>Coutts, Glyn</creatorcontrib><creatorcontrib>Bonington, Suzie</creatorcontrib><creatorcontrib>Carrington, Bernadette</creatorcontrib><creatorcontrib>Taylor, Ben</creatorcontrib><creatorcontrib>Khoo, Saye</creatorcontrib><creatorcontrib>Bonington, Alec</creatorcontrib><title>Utility of FDG-PETCT and magnetic resonance spectroscopy in differentiating between cerebral lymphoma and non-malignant CNS lesions in HIV-infected patients</title><title>European journal of radiology</title><addtitle>Eur J Radiol</addtitle><description>Abstract Background and purpose In HIV infected patients, MRI cannot reliably differentiate between central nervous system (CNS) lymphoma and non-malignant CNS lesions, particularly cerebral toxoplasmosis (CTOX). This study prospectively investigates the utility of FDG PET-CT and magnetic resonance spectroscopy (MRS) in discriminating CNS lymphoma from non-malignant CNS lesions in HIV infected patients, and assesses the ability of FDG PET-CT to guide the use of early brain biopsy. Methods 10 HIV patients with neurological symptoms and contrast enhancing lesions on MRI were commenced on anti-toxoplasmosis therapy before undergoing FDG PET-CT and MRS. Brain biopsies were sought in those with FDG PET-CT suggestive of CNS lymphoma, and in those with a negative FDG PET-CT scan who failed to respond to therapy. Final diagnosis was based on histology or treatment response. Results Two patients were confirmed to have CNS lymphoma and FDG PET-CT was consistent with this diagnosis in both. Six patients had cerebral toxoplasmosis in all of whom FDG PET-CT was consistent with non-malignant disease. One patient had progressive multifocal leukoencephalopathy (PML), FDG PET-CT was equivocal. One patient had a haemorrhagic brain metastasis and FDG PET-CT wrongly suggested non-malignant disease. MRS was performed successfully in eight subjects: three results were suggestive of CNS lymphoma (one true positive, two false positive), four suggested CTOX (two false negative, two true negative), one scan was equivocal. Conclusion FDG PET-CT correctly identified all cases of CNS lymphoma and CTOX, supporting its use in this situation. 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Hogan, Celia ; Julyan, Peter J ; Coutts, Glyn ; Bonington, Suzie ; Carrington, Bernadette ; Taylor, Ben ; Khoo, Saye ; Bonington, Alec</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c480t-d65ef9bb23ad476422ee9f2c7b8c7cc7192e75ecd3b2d75de7ad4bda6c4ff1f13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Biomarkers - analysis</topic><topic>Brain Diseases - diagnosis</topic><topic>Brain Diseases - metabolism</topic><topic>Central nervous system</topic><topic>Diagnosis, Differential</topic><topic>Female</topic><topic>Fluorodeoxyglucose F18</topic><topic>HIV</topic><topic>HIV Infections - diagnosis</topic><topic>HIV Infections - metabolism</topic><topic>Humans</topic><topic>Lymphoma</topic><topic>Lymphoma, AIDS-Related - diagnosis</topic><topic>Lymphoma, AIDS-Related - metabolism</topic><topic>Magnetic resonance spectroscopy</topic><topic>Magnetic Resonance Spectroscopy - methods</topic><topic>Male</topic><topic>Multimodal Imaging - methods</topic><topic>Positron emission tomography and computed tomography</topic><topic>Positron-Emission Tomography - methods</topic><topic>Radiology</topic><topic>Radiopharmaceuticals</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Tomography, X-Ray Computed - methods</topic><topic>United Kingdom</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Westwood, Thomas D</creatorcontrib><creatorcontrib>Hogan, Celia</creatorcontrib><creatorcontrib>Julyan, Peter J</creatorcontrib><creatorcontrib>Coutts, Glyn</creatorcontrib><creatorcontrib>Bonington, Suzie</creatorcontrib><creatorcontrib>Carrington, Bernadette</creatorcontrib><creatorcontrib>Taylor, Ben</creatorcontrib><creatorcontrib>Khoo, Saye</creatorcontrib><creatorcontrib>Bonington, Alec</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of radiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Westwood, Thomas D</au><au>Hogan, Celia</au><au>Julyan, Peter J</au><au>Coutts, Glyn</au><au>Bonington, Suzie</au><au>Carrington, Bernadette</au><au>Taylor, Ben</au><au>Khoo, Saye</au><au>Bonington, Alec</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Utility of FDG-PETCT and magnetic resonance spectroscopy in differentiating between cerebral lymphoma and non-malignant CNS lesions in HIV-infected patients</atitle><jtitle>European journal of radiology</jtitle><addtitle>Eur J Radiol</addtitle><date>2013-08-01</date><risdate>2013</risdate><volume>82</volume><issue>8</issue><spage>e374</spage><epage>e379</epage><pages>e374-e379</pages><issn>0720-048X</issn><eissn>1872-7727</eissn><abstract>Abstract Background and purpose In HIV infected patients, MRI cannot reliably differentiate between central nervous system (CNS) lymphoma and non-malignant CNS lesions, particularly cerebral toxoplasmosis (CTOX). This study prospectively investigates the utility of FDG PET-CT and magnetic resonance spectroscopy (MRS) in discriminating CNS lymphoma from non-malignant CNS lesions in HIV infected patients, and assesses the ability of FDG PET-CT to guide the use of early brain biopsy. Methods 10 HIV patients with neurological symptoms and contrast enhancing lesions on MRI were commenced on anti-toxoplasmosis therapy before undergoing FDG PET-CT and MRS. Brain biopsies were sought in those with FDG PET-CT suggestive of CNS lymphoma, and in those with a negative FDG PET-CT scan who failed to respond to therapy. Final diagnosis was based on histology or treatment response. Results Two patients were confirmed to have CNS lymphoma and FDG PET-CT was consistent with this diagnosis in both. Six patients had cerebral toxoplasmosis in all of whom FDG PET-CT was consistent with non-malignant disease. One patient had progressive multifocal leukoencephalopathy (PML), FDG PET-CT was equivocal. One patient had a haemorrhagic brain metastasis and FDG PET-CT wrongly suggested non-malignant disease. MRS was performed successfully in eight subjects: three results were suggestive of CNS lymphoma (one true positive, two false positive), four suggested CTOX (two false negative, two true negative), one scan was equivocal. Conclusion FDG PET-CT correctly identified all cases of CNS lymphoma and CTOX, supporting its use in this situation. MRS was unhelpful in our cohort.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>23578921</pmid><doi>10.1016/j.ejrad.2013.03.008</doi></addata></record>
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subjects Adult
Biomarkers - analysis
Brain Diseases - diagnosis
Brain Diseases - metabolism
Central nervous system
Diagnosis, Differential
Female
Fluorodeoxyglucose F18
HIV
HIV Infections - diagnosis
HIV Infections - metabolism
Humans
Lymphoma
Lymphoma, AIDS-Related - diagnosis
Lymphoma, AIDS-Related - metabolism
Magnetic resonance spectroscopy
Magnetic Resonance Spectroscopy - methods
Male
Multimodal Imaging - methods
Positron emission tomography and computed tomography
Positron-Emission Tomography - methods
Radiology
Radiopharmaceuticals
Reproducibility of Results
Sensitivity and Specificity
Tomography, X-Ray Computed - methods
United Kingdom
title Utility of FDG-PETCT and magnetic resonance spectroscopy in differentiating between cerebral lymphoma and non-malignant CNS lesions in HIV-infected patients
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