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      Manifestation of lymphoma expansion following lymphatic drainage on 18F-FDG PET/CT

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          Abstract

          18F-fluorodeoxyglucose (FDG) positron emission tomography (PET) imaging is strongly recommended in patients with diffuse large B-cell lymphomas (DLBCL), which are routinely highly FDG avid, for adequate disease staging [1]. The mean standardized uptake value (SUV) can be used to distinguish aggressive from indolent lymphoma variants [2]. PET scanning is a reliable method for the diagnosis of DLBCL compared with the reference method immunohistology [3]. We present a case of a 70-year-old female patient who presented to the hospital with progressive swelling, pain and loss of sensibility in her right lower limb. Nine months earlier she had been diagnosed with DLBLC, localized in the lungs, mediastinum and mesenterium for which she was treated with rituximab plus cyclophosphamide, doxorubicin, vincristine and prednisone (R-CHOP) chemotherapy. 18F-FDG PET/CT scanning was performed for restaging of lymphoma disease in this patient. 18F-FDG PET/CT showed an extensive lesion in the right lower limb, with extremely high avidity for FDG, corresponding with tumour mass in muscular tissue on the low-dose CT (figure). It was spreading upwards, following the lymphatic drainage system and surrounding vessels, up to the right groin region. The SUVmean of this large lesion was 16.4 (calculation conforming to the EANM procedure guidelines for tumour PET imaging [4]). Further on, a lesion was detected dorsally in the right lung. Biopsy of the swelling in the right lower limb revealed aggressive DLBCL recurrence. This aggressive form was already expected due to the high SUVmean value. This scan shows how aggressive DLBCL can appear as a fast growing lymphoma with an atypical configuration by following the lymphatic drainage.

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          FDG PET and PET/CT: EANM procedure guidelines for tumour PET imaging: version 1.0

          The aim of this guideline is to provide a minimum standard for the acquisition and interpretation of PET and PET/CT scans with [18F]-fluorodeoxyglucose (FDG). This guideline will therefore address general information about [18F]-fluorodeoxyglucose (FDG) positron emission tomography-computed tomography (PET/CT) and is provided to help the physician and physicist to assist to carrying out, interpret, and document quantitative FDG PET/CT examinations, but will concentrate on the optimisation of diagnostic quality and quantitative information.
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            Expert opinions on positron emission tomography and computed tomography imaging in lymphoma.

            Revised guidelines for the staging and response criteria of Hodgkin's lymphoma (HL) and non-Hodgkin's lymphoma (NHL) were recently published to include the expanding role of positron emission tomography/computed tomography (PET/CT) using (18)F-fluoro-2-deoxyglucose. Here, we discuss the new guidelines and the need for standardized PET acquisition and interpretation in HL and NHL. We also discuss how the role for CT is evolving in the process of making treatment decisions and provide insight on how best to standardize the use of PET/CT for making therapeutic choices.
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              PET scans in the staging of lymphoma: current status.

              Positron emission tomography (PET) is a novel functional imaging technique that provides several inherent advantages over conventional nuclear scintigraphy. Several studies have suggested a role for PET using the positron emitter fluorine-18 in the diagnosis and follow-up of patients with lymphoma. This review summarizes the existing data evaluating the role of 2-fluoro-2-deoxy-D-glucose (FDG)-PET in both the staging and follow-up of patients with lymphoma. Most studies of PET involve patients with either Hodgkin's disease or diffuse large B-cell non-Hodgkin's lymphoma. PET detects more disease sites above and below the diaphragm on staging of lymphoma than gallium scintigraphy and may have particular utility in the evaluation of the spleen. Moreover, persistently positive PET scans during and after chemotherapy appear to have a high sensitivity for predicting subsequent relapse. A negative PET scan at the end of therapy provides very favorable prognostic information. Persistently positive PET scans at the end of therapy warrant close follow-up or additional diagnostic procedures, since some of those patients may remain in prolonged remission. Clearly, additional studies, including prospective blinded trials and cost-effectiveness analyses, are warranted to determine which subsets of patients with lymphoma ultimately will benefit from this modality.
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                Author and article information

                Contributors
                a.w.j.m.glaudemans@ngmb.umcg.nl
                Journal
                Eur J Nucl Med Mol Imaging
                European Journal of Nuclear Medicine and Molecular Imaging
                Springer-Verlag (Berlin/Heidelberg )
                1619-7070
                1619-7089
                7 May 2011
                7 May 2011
                November 2011
                : 38
                : 11
                : 2100-2101
                Affiliations
                [1 ]Department of Nuclear Medicine and Molecular Imaging, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
                [2 ]Ghent University, Ghent, Belgium
                Article
                1822
                10.1007/s00259-011-1822-0
                3188706
                21553089
                75182afd-e183-4131-aa05-5de7fa6e3bcf
                © The Author(s) 2011
                History
                : 27 January 2011
                : 6 April 2011
                Categories
                Image of the Month
                Custom metadata
                © Springer-Verlag 2011

                Radiology & Imaging
                Radiology & Imaging

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