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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">KJIM</journal-id>
<journal-title-group>
<journal-title>The Korean Journal of Internal Medicine</journal-title><abbrev-journal-title>Korean J Intern Med</abbrev-journal-title></journal-title-group>
<issn pub-type="ppub">1226-3303</issn>
<issn pub-type="epub">2005-6648</issn>
<publisher>
<publisher-name>The Korean Association of Internal Medicine</publisher-name></publisher></journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3904/kjim.2017.145</article-id>
<article-id pub-id-type="publisher-id">kjim-2017-145</article-id>
<article-categories>
<subj-group>
<subject>Image of interest</subject></subj-group></article-categories>
<title-group>
<article-title>Radiation nephritis: <sup>99m</sup>Tc hydroxydiphosphonate bone scan, <sup>99m</sup>Tc dimercaptosuccinic acid renal scan, and <sup>18</sup>F-FDG PET/CT findings</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Park</surname><given-names>Hye Lim</given-names></name>
<xref ref-type="aff" rid="af1-kjim-2017-145"><sup>1</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Yoo</surname><given-names>Ie Ryung</given-names></name>
<xref ref-type="corresp" rid="c1-kjim-2017-145"/>
<xref ref-type="aff" rid="af1-kjim-2017-145"><sup>1</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Kim</surname><given-names>Yeon Sil</given-names></name>
<xref ref-type="aff" rid="af2-kjim-2017-145"><sup>2</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Kang</surname><given-names>Jin-Hyoung</given-names></name>
<xref ref-type="aff" rid="af3-kjim-2017-145"><sup>3</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Lee</surname><given-names>Ji Eun</given-names></name>
<xref ref-type="aff" rid="af3-kjim-2017-145"><sup>3</sup></xref>
</contrib>
<aff id="af1-kjim-2017-145">
<label>1</label>Division of Nuclear Medicine, Department of Radiology, The Catholic University of Korea, Seoul, <country>Korea</country></aff>
<aff id="af2-kjim-2017-145">
<label>2</label>Department of Radiation Oncology, The Catholic University of Korea, Seoul, <country>Korea</country></aff>
<aff id="af3-kjim-2017-145">
<label>3</label>Division of Medical Oncology, Department of Internal Medicine, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, <country>Korea</country></aff>
</contrib-group>
<author-notes>
<corresp id="c1-kjim-2017-145">Correspondence to Ie Ryung Yoo, M.D. Tel: +82-2-2258-1552 Fax: +82-2-2258-1575 E-mail: <email>iryoo@catholic.ac.kr</email></corresp>
</author-notes>
<pub-date pub-type="ppub">
<month>7</month>
<year>2018</year></pub-date>
<pub-date pub-type="epub">
<day>1</day>
<month>11</month>
<year>2017</year></pub-date>
<volume>33</volume>
<issue>4</issue>
<fpage>837</fpage>
<lpage>838</lpage>
<history>
<date date-type="received">
<day>21</day>
<month>03</month>
<year>2017</year></date>
<date date-type="rev-recd">
<day>14</day>
<month>05</month>
<year>2017</year></date>
<date date-type="accepted">
<day>14</day>
<month>05</month>
<year>2017</year></date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2018 The Korean Association of Internal Medicine</copyright-statement>
<copyright-year>2018</copyright-year>
<license>
<license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by-nc/3.0/">http://creativecommons.org/licenses/by-nc/3.0/</ext-link>) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p></license></permissions>
</article-meta></front>
<body>
<p>A 20-year-old male had Ewing&#x02019;s sarcoma of the right paraspinal region (T12&#x02013;L2 vertebra level) and was treated with chemotherapy and radiation therapy (RT). <sup>99m</sup>Tc hydroxydiphosphonate bone scan was performed 4 months after the end of treatment. Intense uptake was noted in both kidneys (<xref rid="f1-kjim-2017-145" ref-type="fig">Fig. 1</xref>). On the fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) for response evaluation, mild uptake was also seen in both kidneys (<xref rid="f2-kjim-2017-145" ref-type="fig">Fig. 2A</xref> and <xref rid="f2-kjim-2017-145" ref-type="fig">2B</xref>). On <sup>99m</sup>Tc dimercaptosuccinic acid (DMSA) scan, photon defects were noted in both kidneys (<xref rid="f2-kjim-2017-145" ref-type="fig">Fig. 2C</xref>). When we reviewed the RT plan, the medial aspect of both kidneys was included in the radiation field (<xref rid="f2-kjim-2017-145" ref-type="fig">Fig. 2D</xref> and <xref rid="f2-kjim-2017-145" ref-type="fig">2E</xref>). On contrast-enhanced CT, low-densities were noted in both kidneys (<xref rid="f2-kjim-2017-145" ref-type="fig">Fig. 2F</xref>). We thus diagnosed radiation nephritis (RN). On 6-month follow-up bone scan, the previously noted intensity on both kidneys was decreased.</p>
<p>RN is commonly seen following RT of intra-abdominal tumors or bony metastasis of spine. The histologic findings are vascular sclerosis with tubular ischemic change. Tubular dysfunction and ischemic change explain the photon defect on DMSA scan and the delayed enhancement and retention of contrast on CT. Delayed excretion of radiopharmaceuticals could cause increased uptake on bone scan. CT and bone scan findings were previously reported, but PET/CT findings were reported in only one case. Although the exact mechanism of increased activity on PET/CT remains uncertain, delayed tracer excretion via parenchymal injury could be a major cause. Radiation-induced inflammation can also cause. However, the lack of evidence of inflammation in other tissues included in the radiation field and the decreased blood flow to the kidneys on enhanced CT indicate that the inflammation was a minor contributor.</p>
<p>Focal renal activity on PET/CT could be misinterpreted as malignancy. Differential diagnostic criteria for distinguishing RN from malignancy include a RT history, a linear uptake pattern, and a sharp margin of uptake. Lesion locations were the medial or upper portion of the kidney. Clinicians need to exclude RN when linear increases in renal activity are incidentally detected on FDG PET/CT.</p>
</body>
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<fn-group>
<fn fn-type="conflict"><p>No potential conflict of interest relevant to this article was reported.</p></fn>
</fn-group>
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<title>Figures</title>
<fig id="f1-kjim-2017-145" position="float">
<label>Figure 1.</label><caption><p>On <sup>99m</sup>Tc hydroxydiphosphonate bone scan 4 months after radiotherapy for evaluation of metastasis, intense linear band-like uptake was noted in the medial aspect of both kidneys (arrows). </p></caption>
<graphic xlink:href="kjim-2017-145f1.tif"/>
</fig>
<fig id="f2-kjim-2017-145" position="float">
<label>Figure 2.</label><caption><p>On the same day with bone scan, fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) was performed. (A, B) Mild longitudinal uptake was seen in the medial aspect of both kidneys on <sup>18</sup>F-FDG PET/CT (arrows). (C) Five days later, <sup>99m</sup>Tc dimercaptosuccinic acid scan was performed to evaluate functional impairment, and photon defects were noted in the medial aspect of the renal cortices. Urea nitrogen and creatinine were within normal range (11.6 and 0.79 mg/dL). (D, E) These regions were included in the radiation field. Radiation therapy (RT) was delivered to the planning target volume at a dose of 30 Gy in 15 fractions using a three-dimensional RT technique followed by a boost of 20 Gy in 10 fractions using intensity-modulated radiotherapy, up to a total dose of 50 Gy in 25 fractions. (F) On contrast-enhanced abdominal CT, the medial aspects of both kidneys were a well-marginated, low density area.</p></caption>
<graphic xlink:href="kjim-2017-145f2.tif"/>
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