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      Fluorodeoxyglucose Uptake in Lipomatous Hypertrophy of the Interatrial Septum is Not Likely Related to Brown Adipose Tissue

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          Abstract

          Dear Editor, We read with interest the article by Kamaleshwaran et al.[1] and found that our previous publication[2] was cited twice, that is, (1) as a reference for the prevalence of lipomatous hypertrophy of the interatrial septum (LHIS) on echocardiography and (2) for the concept that inflammation is the cause of increased fluorodeoxyglucose (FDG) uptake in LHIS. First, our paper is not a reference for the prevalence of LHIS on echocardiography. Our paper: “FDG uptake in LHIS is not likely related to brown adipose tissue (BAT)” should have been cited as a report suggesting increased FDG uptake in LHIS is not likely related to BAT, as its title suggests. Dual-time point imaging may be useful to help distinguish FDG uptake associated with benign versus malignant etiologies;[3] However, it should be remembered that no imaging test or criteria are 100% sensitive/specific. Washout of FDG does not necessarily confirm an inflammatory etiology. Indeed, 5 of 18 benign lesions in reference 3 did not show FDG washout on delayed imaging. In particular, 3 of these 5 benign lesions showed an increase in FDG avidity with time that is, 10%, 13% and 27%. We have certainly seen cases where inflammatory lesions showed an increase in FDG uptake on delayed imaging. We hope an amendment to the paper by Kamaleshwaran et al.[1] can be published to prevent a misconception from developing. Specifically, our paper is not a reference for the prevalence of LHIS on echocardiography. Further, we did not prove that inflammation is the cause of increased FDG uptake in LHIS but suggested it only as a “possible” alternative cause. At the same time, Kamaleshwaran et al.'s paper does not disprove it. As we mentioned in our previous paper, we would like to re-emphasize that a larger sample size would be needed to show whether inflammation is indeed the cause of increased FDG uptake associated with LHIS or not. Our paper suggested FDG uptake in LHIS is not likely related to BAT (we were likely the first to suggest this) and our paper is a reference for this. Thank you for your help in this matter. We would sincerely appreciate that the reference to our paper is correct.

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          Potential of dual-time-point imaging to improve breast cancer diagnosis with (18)F-FDG PET.

          The purpose of this study was to assess the utility of dual-time-point imaging for identifying malignant lesions in the breast by (18)F-FDG PET. Fifty-four breast cancer patients with 57 breast lesions underwent 2 sequential PET scans (dual-time-point imaging). The average percent change in standardized uptake values (SUVs) between time point 1 and time point 2 was calculated. All PET study results were correlated with follow-up surgical pathology results. Of the 57 breast lesions, 39 were invasive carcinoma and 18 were postbiopsy inflammation. Among the invasive carcinoma lesions, 33 (85%) showed an increase and 6 (15%) showed either no change or a decrease in SUVs over time. The percent change in SUVs from time point 1 to time point 2 (mean +/- SD) was +12.6% +/- 11.4% (P = 0.003). Of the 18 inflammatory lesions, 3 (17%) showed an increase and 15 (83%) showed either no change or a decrease in SUVs. The percent change in SUVs from time point 1 to time point 2 (mean +/- SD) was -10.2% +/- 16.5% (P = 0.03). Of the 57 normal contralateral breasts, 2 (3.5%) showed an increase and 55 (96.5%) showed either no change or a decrease in SUVs. The percent change in SUVs from time point 1 to time point 2 (mean +/- SD) was -15.8% +/- 17% (P = 0.005). There is increasing uptake of (18)F-FDG over time in breast malignancies, whereas the uptake of (18)F-FDG in inflammatory lesions and normal breast tissues decreases over time. A percent change of +3.75 or more in SUVs over time is highly sensitive and specific in differentiating inflammatory lesions from malignant lesions.
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            FDG uptake in lipomatous hypertrophy of the interatrial septum is not likely related to brown adipose tissue.

            Lipomatous hypertrophy of the interatrial septum (LHIS) may be associated with arrhythmias or sudden death. Increased fluorine-18 fluorodeoxyglucose (FDG) uptake in LHIS is occasionally found on positron emission tomography, and has been attributed to metabolically active brown adipose tissue (BAT) contained within LHIS. We report a case of a patient suggesting that neither of the 2 currently known mechanisms of glucose uptake by BAT is responsible for FDG uptake in LHIS, unless a mechanism of BAT activation exists that has not been previously described. This study also suggests that FDG uptake is unlikely to be due to cardiomyocytes contained within LHIS. Inflammation is a potential mechanism, although further investigation is needed.
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              Persistent High Grade Flurodeoxyglucose Uptake in Lipomatous Hypertrophy of the Interatrial Septum on Dual Time Point Imaging and with Ambient Warming

              Lipomatous hypertrophy of the interatrial septum (LHIS) is a relatively uncommon disorder of the heart characterized by benign fatty infiltration of the interatrial septum that usually spares the fossa ovalis. LHIS showing flurodeoxyglucose uptake has been reported, and is presumed to be due to activated brown adipose tissue (BAT). We here report a case of a patient who had isolated mediastinal uptake in interatrial septum, mimicking metastasis. Rescanning with external warming to deactivate BAT and a delayed time point image was done, which showed persistent and progressively increasing metabolic uptake respectively, suggesting that LHIS uptake might be unrelated to activated BAT or inflammation.
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                Author and article information

                Journal
                World J Nucl Med
                World J Nucl Med
                WJNM
                World Journal of Nuclear Medicine
                Medknow Publications & Media Pvt Ltd (India )
                1450-1147
                1607-3312
                Jan-Apr 2015
                : 14
                : 1
                : 72
                Affiliations
                [1]Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02026, United States
                [1 ]Department of Medical Imaging, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, ON M4N 3M5, Canada
                Author notes
                Address for correspondence: Dr. Chun K. Kim, 75 Francis Street, Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02026, United States. E-mail: ckkim@ 123456bwh.harvard.edu
                Article
                WJNM-14-72
                10.4103/1450-1147.150567
                4337018
                25709555
                a1d479de-a2a5-45c6-8ea4-9322959636a0
                Copyright: © World Journal of Nuclear Medicine

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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                Letter to Editor

                Radiology & Imaging
                Radiology & Imaging

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