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<article xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" article-type="letter"><?properties open_access?><front><journal-meta><journal-id journal-id-type="nlm-ta">Korean J Intern Med</journal-id><journal-id journal-id-type="iso-abbrev">Korean J. Intern. Med</journal-id><journal-id journal-id-type="publisher-id">KJIM</journal-id><journal-title-group><journal-title>The Korean Journal of Internal Medicine</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="pmid">23682234</article-id><article-id pub-id-type="pmc">3654138</article-id><article-id pub-id-type="doi">10.3904/kjim.2013.28.3.370</article-id><article-categories><subj-group subj-group-type="heading"><subject>Letter to the Editor</subject></subj-group></article-categories><title-group><article-title>Spontaneous coronary artery dissection diagnosed by intravascular ultrasound and followed up by cardiac computed tomography</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Choi</surname><given-names>Sang-Woong</given-names></name><xref ref-type="aff" rid="A1-kjim-28-370"/></contrib><contrib contrib-type="author" corresp="yes"><name><surname>Nam</surname><given-names>Chang-Wook</given-names></name><xref ref-type="aff" rid="A1-kjim-28-370"/></contrib><contrib contrib-type="author"><name><surname>Bae</surname><given-names>Han-Jun</given-names></name><xref ref-type="aff" rid="A1-kjim-28-370"/></contrib><contrib contrib-type="author"><name><surname>Cho</surname><given-names>Yun-Kyeong</given-names></name><xref ref-type="aff" rid="A1-kjim-28-370"/></contrib><contrib contrib-type="author"><name><surname>Yoon</surname><given-names>Hyuck-Jun</given-names></name><xref ref-type="aff" rid="A1-kjim-28-370"/></contrib><contrib contrib-type="author"><name><surname>Hur</surname><given-names>Seung-Ho</given-names></name><xref ref-type="aff" rid="A1-kjim-28-370"/></contrib><contrib contrib-type="author"><name><surname>Kim</surname><given-names>Kwon-Bae</given-names></name><xref ref-type="aff" rid="A1-kjim-28-370"/></contrib></contrib-group><aff id="A1-kjim-28-370">Division of Cardiology, Department of Internal Medicine, Keimyung University Dongsan Medical Center, Daegu, Korea.</aff><author-notes><corresp>
Correspondence to Chang-Wook Nam, M.D. Division of Cardiology, Department of Internal Medicine, Keimyung University Dongsan Medical Center, 56 Dalseong-ro, Jung-gu, Daegu 700-712, Korea. Tel: +82-53-250-8015, Fax: +82-53-250-7034, <email>ncwcv@dsmc.or.kr</email></corresp></author-notes><pub-date pub-type="ppub"><month>5</month><year>2013</year></pub-date><pub-date pub-type="epub"><day>01</day><month>5</month><year>2013</year></pub-date><volume>28</volume><issue>3</issue><fpage>370</fpage><lpage>373</lpage><history><date date-type="received"><day>15</day><month>1</month><year>2012</year></date><date date-type="rev-recd"><day>02</day><month>4</month><year>2012</year></date><date date-type="accepted"><day>03</day><month>4</month><year>2012</year></date></history><permissions><copyright-statement>Copyright &#xA9; 2013 The Korean Association of Internal Medicine</copyright-statement><copyright-year>2013</copyright-year><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc/3.0/"><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 non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p></license></permissions><kwd-group><kwd>Coronary artery dissection, spontaneous</kwd><kwd>Ultrasonography, interventional</kwd><kwd>Computed tomography</kwd></kwd-group></article-meta></front><body><p>To the Editor,</p><p>Although spontaneous coronary artery dissection (SCAD) is well known clinically, the diagnosis of SCAD is occasionally difficult using only conventional coronary angiography (CAG) without additional imaging tools such as intravascular ultrasound (IVUS) or cardiac computed tomography (CCT).</p><p>A 55-year-old woman presented to the emergency department with resting anterior chest pain after emotional stress. She had a 7-year history of hypertension. Electrocardiography and transthoracic echocardiography results were unremarkable, and CCT was performed to evaluate the cause of the chest pain. This revealed severe luminal narrowing in the middle part of the left anterior descending coronary artery (LAD) (<xref ref-type="fig" rid="F1-kjim-28-370">Fig. 1A</xref>). CAG showed 60% stenosis of the middle to distal LAD (<xref ref-type="fig" rid="F1-kjim-28-370">Fig. 1B</xref>). IVUS to evaluate the lesion revealed coronary artery dissection and a hematoma in the middle LAD, from the 2nd diagonal to the 4th septal branch (<xref ref-type="fig" rid="F1-kjim-28-370">Fig. 1C and 1D</xref>). As there was no coronary flow limitation and the symptoms stabilized, the patient was managed medically without additional procedures. The 3-month follow-up CCT showed resolution of the compressed luminal narrowing (<xref ref-type="fig" rid="F1-kjim-28-370">Fig. 1E</xref>).</p><p>A 70-year-old man presented to the emergency department with sudden-onset severe resting chest pain for 30 minutes. Electrocardiography showed ST segment elevation in leads I and aVL. Emergency CAG revealed mild stenosis in the proximal LAD and left circumflex coronary artery (LCX) (<xref ref-type="fig" rid="F2-kjim-28-370">Fig. 2A</xref>). The ST-segment elevation resolved spontaneously. IVUS revealed coronary artery dissection and a hematoma from the left main (LM) to the proximal LAD and proximal LCX (<xref ref-type="fig" rid="F2-kjim-28-370">Fig. 2B and 2C</xref>). The patient was treated medically due to stabilized symptom. One week later, CCT revealed a minimal residual hematoma in the left main bifurcation area (<xref ref-type="fig" rid="F2-kjim-28-370">Fig. 2D</xref>).</p><p>SCAD is a rare cause of acute coronary syndrome. The clinical presentation can range from angina to ST segment elevation myocardial infarction, ventricular fibrillation, and sudden death [<xref ref-type="bibr" rid="B1-kjim-28-370">1</xref>]. SCAD is a hematoma or thrombus in a false lumen, usually in the outer third layer of the coronary artery wall; this compresses the true lumen and leads to coronary ischemia [<xref ref-type="bibr" rid="B2-kjim-28-370">2</xref>]. SCAD should be considered in patients, especially women in the peripartum period and those using oral contraceptives, who complain of chest pain and have atherosclerosis or cardiovascular risk factors, or vascular disease. Other risk factors are connective tissue disorders, cocaine use, exercise, and medications such as 5-fluorouracil, cyclosporine, and fenfluramine.</p><p>The etiology and pathophysiology of SCAD are poorly understood [<xref ref-type="bibr" rid="B3-kjim-28-370">3</xref>]. The optimal treatment strategy for SCAD remains undetermined, and treatment varies according to the type and severity of presentation [<xref ref-type="bibr" rid="B4-kjim-28-370">4</xref>]. Treatment options include percutaneous coronary intervention, coronary artery bypass grafting, and conservative medical management such as a &#x3B2;-blocker to reduce the vascular shear forces and antiplatelet therapy to reduce thrombus formation. The choice is based on the patient's hemodynamic status, coronary artery flow, dissection location, number of involved vessels, and other clinical situations.</p><p>The diagnosis of SCAD is made principally based on the appearance of a radiolucent intimal flap or slow clearance of contrast from the false lumen on CAG. When an intimal tear is absent, the medial hematoma can appear as a narrowed or occluded vessel on CAG. The true incidence of SCAD can be underestimated when diagnosed using CAG alone [<xref ref-type="bibr" rid="B5-kjim-28-370">5</xref>]. Imaging tools such as CCT and IVUS can support the diagnosis of SCAD. IVUS can distinguish atherosclerotic stenosis and spasm from hematoma or dissection, and can identify the length of the hematoma or location of the dissection. In addition, IVUS can be used during percutaneous coronary intervention for SCAD. IVUS can facilitate the placement of the angioplasty guidewire within the true lumen; assist in determining stent size, length, and optimal deployment; and ensure obliteration of the false lumen and flow within it, or adequate compression of the intramural hematoma [<xref ref-type="bibr" rid="B5-kjim-28-370">5</xref>]. CCT is an ideal noninvasive imaging technique for delineating intramural hematomas and assessing luminal narrowing. Furthermore, follow-up of SCAD without invasive diagnostic CAG is an important benefit of CCT, as in our cases. To make the diagnosis, a clinical suspicion of SCAD is important when it is difficult to explain the pathogenesis of a stenotic lesion, especially in young patients with no conventional risk factors.</p><p>In conclusion, SCAD is an unusual cause of acute coronary syndrome and is difficult to diagnose. Therefore, a clinical suspicion of SCAD and the use of additional imaging tools such as IVUS and CCT are vital. In the presented cases, SCAD was diagnosed successfully using IVUS and followed up using CCT.</p></body><back><fn-group><fn fn-type="conflict"><p>No potential conflict of interest relevant to this article is reported.</p></fn></fn-group><ref-list><ref id="B1-kjim-28-370"><label>1</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Vanzetto</surname><given-names>G</given-names></name><name><surname>Berger-Coz</surname><given-names>E</given-names></name><name><surname>Barone-Rochette</surname><given-names>G</given-names></name><etal/></person-group><article-title>Prevalence, therapeutic management and medium-term prognosis of spontaneous coronary artery dissection: results from a database of 11,605 patients</article-title><source>Eur J Cardiothorac Surg</source><year>2009</year><volume>35</volume><fpage>250</fpage><lpage>254</lpage><pub-id pub-id-type="pmid">19046896</pub-id></element-citation></ref><ref id="B2-kjim-28-370"><label>2</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Adlam</surname><given-names>D</given-names></name><name><surname>Cuculi</surname><given-names>F</given-names></name><name><surname>Lim</surname><given-names>C</given-names></name><name><surname>Banning</surname><given-names>A</given-names></name></person-group><article-title>Management of spontaneous coronary artery dissection in the primary percutaneous coronary intervention era</article-title><source>J Invasive Cardiol</source><year>2010</year><volume>22</volume><fpage>549</fpage><lpage>553</lpage><pub-id pub-id-type="pmid">21041853</pub-id></element-citation></ref><ref id="B3-kjim-28-370"><label>3</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Almafragi</surname><given-names>A</given-names></name><name><surname>Convens</surname><given-names>C</given-names></name><name><surname>Heuvel</surname><given-names>PV</given-names></name></person-group><article-title>Spontaneous healing of spontaneous coronary artery dissection</article-title><source>Cardiol J</source><year>2010</year><volume>17</volume><fpage>92</fpage><lpage>95</lpage><pub-id pub-id-type="pmid">20104464</pub-id></element-citation></ref><ref id="B4-kjim-28-370"><label>4</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Almeda</surname><given-names>FQ</given-names></name><name><surname>Barkatullah</surname><given-names>S</given-names></name><name><surname>Kavinsky</surname><given-names>CJ</given-names></name></person-group><article-title>Spontaneous coronary artery dissection</article-title><source>Clin Cardiol</source><year>2004</year><volume>27</volume><fpage>377</fpage><lpage>380</lpage><pub-id pub-id-type="pmid">15298035</pub-id></element-citation></ref><ref id="B5-kjim-28-370"><label>5</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Arnold</surname><given-names>JR</given-names></name><name><surname>West</surname><given-names>NE</given-names></name><name><surname>van Gaal</surname><given-names>WJ</given-names></name><name><surname>Karamitsos</surname><given-names>TD</given-names></name><name><surname>Banning</surname><given-names>AP</given-names></name></person-group><article-title>The role of intravascular ultrasound in the management of spontaneous coronary artery dissection</article-title><source>Cardiovasc Ultrasound</source><year>2008</year><volume>6</volume><fpage>24</fpage><pub-id pub-id-type="pmid">18513437</pub-id></element-citation></ref></ref-list></back><floats-group><fig id="F1-kjim-28-370" position="float"><label>Figure 1</label><caption><p>(A) Cardiac computed tomography (CT) revealed luminal narrowing in the middle part of the left anterior descending (LAD) coronary artery. (B) Coronary angiography revealed 60% stenosis of the middle to distal LAD. (C) Intravascular ultrasound (IVUS; sagittal view) showed coronary artery dissection and a hematoma in the middle part of the LAD. (D) IVUS (longitudinal view) showed coronary artery dissection and a diffuse hematoma in the LAD. (E) The 3-month follow-up multidetector CT showed resolution of the compressed luminal narrowing.</p></caption><graphic xlink:href="kjim-28-370-g001"/></fig><fig id="F2-kjim-28-370" position="float"><label>Figure 2</label><caption><p>(A) Coronary angiography revealed mild stenosis in the proximal parts of the left anterior descending (LAD) and left circumflex coronary artery (LCX). (B, C) Intravascular ultrasound showed coronary artery dissection and a hematoma extending from the left main (LM) to the proximal LAD and LCX. (D) One week later, cardiac computed tomography revealed minimal residual hematoma in the LM bifurcation area.</p></caption><graphic xlink:href="kjim-28-370-g002"/></fig></floats-group></article>
