<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//TaxonX//DTD Taxonomic Treatment Publishing DTD v0 20100105//EN" "https://foliamedica.bg/nlm/tax-treatment-NS0.dtd">
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:tp="http://www.plazi.org/taxpub" article-type="research-article" dtd-version="3.0" xml:lang="en">
  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">87</journal-id>
      <journal-id journal-id-type="index">urn:lsid:arphahub.com:pub:A116C711-4C18-5A38-8F1E-5E97753A8A64</journal-id>
      <journal-title-group>
        <journal-title xml:lang="en">Folia Medica</journal-title>
        <abbrev-journal-title xml:lang="en">FM</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="ppub">0204-8043</issn>
      <issn pub-type="epub">1314-2143</issn>
      <publisher>
        <publisher-name>Plovdiv Medical University</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.3897/folmed.67.e142295</article-id>
      <article-id pub-id-type="publisher-id">142295</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Case Report</subject>
        </subj-group>
        <subj-group subj-group-type="scientific_subject">
          <subject>Diagnostic medicine</subject>
          <subject>Infectious diseases</subject>
          <subject>Radiology &amp; Imaging</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>﻿Fungal embolism of the infrarenal aorta – a life-threatening complication of endocarditis</article-title>
      </title-group>
      <contrib-group content-type="authors">
        <contrib contrib-type="author" corresp="yes">
          <name name-style="western">
            <surname>Anastasiadou</surname>
            <given-names>Christiana</given-names>
          </name>
          <email xlink:type="simple">an.xristiana@hotmail.com</email>
          <uri content-type="orcid">https://orcid.org/0000-0001-7260-9534</uri>
          <xref ref-type="aff" rid="A1">1</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Pujante</surname>
            <given-names>Antonio</given-names>
          </name>
          <xref ref-type="aff" rid="A2">2</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Giankoulof</surname>
            <given-names>Christos</given-names>
          </name>
          <xref ref-type="aff" rid="A3">3</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Siozos</surname>
            <given-names>Konstantinos</given-names>
          </name>
          <uri content-type="orcid">https://orcid.org/0009-0004-1901-3909</uri>
          <xref ref-type="aff" rid="A4">4</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Aggelopoulos</surname>
            <given-names>Stamatios</given-names>
          </name>
          <xref ref-type="aff" rid="A5">5</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Megalopoulos</surname>
            <given-names>Angelos</given-names>
          </name>
          <xref ref-type="aff" rid="A1">1</xref>
        </contrib>
      </contrib-group>
      <aff id="A1">
        <label>1</label>
        <addr-line content-type="verbatim">Department of Vascular Surgery, George Papanikolaou General Hospital of Thessaloniki, Thessaloniki, Greece</addr-line>
        <institution>Department of Vascular Surgery – General Hospital of Thessaloniki “George Papanikolaou</institution>
        <addr-line content-type="city">Thessaloniki</addr-line>
        <country>Greece</country>
      </aff>
      <aff id="A2">
        <label>2</label>
        <addr-line content-type="verbatim">Surgical Department, George Papanikolaou General Hospital of Thessaloniki, Thessaloniki, Greece</addr-line>
        <institution>Surgical Department George Papanikolaou General Hospital of Thessaloniki</institution>
        <addr-line content-type="city">Thessaloniki</addr-line>
        <country>Greece</country>
      </aff>
      <aff id="A3">
        <label>3</label>
        <addr-line content-type="verbatim">Radiology Department, George Papanikolaou General Hospital of Thessaloniki, Thessaloniki, Greece</addr-line>
        <institution>Radiology Department - General Hospital of Thessaloniki “George Papanikolaou”</institution>
        <addr-line content-type="city">Thessaloniki</addr-line>
        <country>Greece</country>
      </aff>
      <aff id="A4">
        <label>4</label>
        <addr-line content-type="verbatim">Fourth Academic Surgical Department, George Papanikolaou General Hospital of Thessaloniki, Thessaloniki, Greece</addr-line>
        <institution>4th Academic Surgical Department – General Hospital of Thessaloniki “George Papanikolaou</institution>
        <addr-line content-type="city">Thessaloniki</addr-line>
        <country>Greece</country>
      </aff>
      <aff id="A5">
        <label>5</label>
        <addr-line content-type="verbatim">Fourth Department of Surgery, Medical School, Aristotle University of Thessaloniki, Georgios Papanikolaou General Hospital of Thessaloniki, Thessaloniki, Greece</addr-line>
        <institution>Aristotle University of Thessaloniki</institution>
        <addr-line content-type="city">Thessaloniki</addr-line>
        <country>Greece</country>
      </aff>
      <author-notes>
        <fn fn-type="corresp">
          <p>Corresponding author: Christiana Anastasiadou, Department of Vascular Surgery, George Papanikolaou General Hospital of Thessaloniki, Thessaloniki, Greece; Email: <email xlink:type="simple">an.xristiana@hotmail.com</email></p>
        </fn>
      </author-notes>
      <pub-date pub-type="collection">
        <year>2025</year>
      </pub-date>
      <pub-date pub-type="epub">
        <day>14</day>
        <month>08</month>
        <year>2025</year>
      </pub-date>
      <volume>67</volume>
      <issue>4</issue>
      <elocation-id>e142295</elocation-id>
      <uri content-type="arpha" xlink:href="http://openbiodiv.net/1B192872-55A6-5AC0-A9F8-8796ED23B8C5">1B192872-55A6-5AC0-A9F8-8796ED23B8C5</uri>
      <history>
        <date date-type="received">
          <day>20</day>
          <month>11</month>
          <year>2024</year>
        </date>
        <date date-type="accepted">
          <day>08</day>
          <month>01</month>
          <year>2025</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>Christiana Anastasiadou, Antonio Pujante, Christos Giankoulof, Konstantinos Siozos, Stamatios Aggelopoulos, Angelos Megalopoulos</copyright-statement>
        <license license-type="creative-commons-attribution" xlink:href="http://creativecommons.org/licenses/by/4.0/" xlink:type="simple">
          <license-p>This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
        </license>
      </permissions>
      <abstract>
        <label>Abstract</label>
        <p>Fungal embolism of the infrarenal aorta is a rare but critical complication of infective endocarditis, associated with significant morbidity and mortality. Outcomes depend heavily on timely detection and management. Here, we present an extremely rare case of acute aortic occlusion caused by <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Candida">Candida</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="albicans">albicans</tp:taxon-name-part></tp:taxon-name></italic> originating from a valve other than the one that was replaced. This report emphasizes the importance of recognizing atypical manifestations of endocarditis in clinical practice and the need for early antifungal therapy in high-risk patients.</p>
      </abstract>
      <kwd-group>
        <label>Keywords</label>
        <kwd>aorta embolism</kwd>
        <kwd>endocarditis</kwd>
        <kwd>fungal</kwd>
        <kwd>septic embolism</kwd>
      </kwd-group>
    </article-meta>
    <notes>
      <sec sec-type="Citation" id="SECID0EJF">
        <title>Citation</title>
        <p>Anastasiadou C, Pujante A, Giankoulof C, Siozos K, Aggelopoulos S, Megalopoulos A. Fungal embolism of the infrarenal aorta – a life-threatening complication of endocarditis. Folia Med (Plovdiv) 2025;67(4):e142295. doi: <ext-link xlink:type="simple" ext-link-type="doi" xlink:href="10.3897/folmed.67.e142295">10.3897/folmed.67.e142295</ext-link>.</p>
      </sec>
    </notes>
  </front>
  <body>
    <sec sec-type="Introduction" id="SECID0EVF">
      <title>Introduction</title>
      <p>Acute thromboembolic occlusion of the infrarenal aorta is a serious clinical condition. It occurs when a blood clot travels through the arterial system and becomes lodged in the aorta below the renal arteries. Common risk factors include cardiac conditions such as atrial fibrillation and valvular heart disease, as well as vascular conditions such as atherosclerosis and aneurysms. Key determinants of prognosis include early diagnosis and revascularization within six hours.<sup>[<xref ref-type="bibr" rid="B1">1</xref>]</sup> In cases where the condition is accompanied by an infectious pathogen, it is referred to as septic embolism, a condition that is associated with an increased risk of morbidity and mortality. In this study, we present a rare case of acute aortic occlusion caused by <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Candida">Candida</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="albicans">albicans</tp:taxon-name-part></tp:taxon-name></italic>. Informed consent has been obtained from the patient for the publication of this case report and its associated images.</p>
    </sec>
    <sec sec-type="Case report" id="SECID0ENG">
      <title>Case report</title>
      <p><italic>An 80-year-old man was transferred from a secondary care hospital due to the sudden onset of acute lumbar pain and paraplegia, accompanied by cold and pale lower limbs. Upon examination, pulselessness of the extremities, hypoesthesia, and paraplegia were noted. A computerized tomography angiography (<abbrev xlink:title="computerized tomography angiography" id="ABBRID0EVG">CTA</abbrev>) scan revealed occlusion of the distal abdominal aorta, the common iliac arteries, and the inferior mesenteric artery</italic><bold><italic>(Fig. <xref ref-type="fig" rid="F1">1</xref>)</italic></bold>. <italic>Additionally, renal infarction of the lower pole of the left kidney was revealed. The patient’s medical history included congestive heart failure, hyperuricemia, dyslipidemia, and arterial hypertension. The patient had undergone aortic valve replacement (bioprosthetic) six months ago. A month ago, the patient was admitted to a secondary care hospital due to pyrexia. During the fever investigation, an echocardiography exam was performed, which revealed the presence of a mobile echogenic mass in the posterior glottis of the mitral valve (1.32×0.7 cm, mildly irregular, with asynchronous motion with the wall)</italic><bold><italic>(Fig. <xref ref-type="fig" rid="F2">2</xref>)</italic></bold>, <italic>raising the suspicion of endocarditis. Blood cultures were negative at that time</italic>﻿. <italic>We initiated intravenous administration of antibiotics (meropenem 2 g three times a day and vancomycin 1 g twice daily), which resulted in resolution of the fever and a gradual decline in inflammatory markers (white blood cell count of 9.68 K/μL, normal range 4–10 K/μL; procalcitonin level of 0.080 ng/mL, normal value &lt;0.05; C-reactive protein level of 4.48 ng/mL, normal range 0.0–0.5 ng/mL). However, subsequent aortic embolism occurred and the patient was then transferred to our hospital.</italic> ﻿<italic>At the time of presentation to our hospital, the inflammatory markers were WBC 11.700 K/μL, procalcitonin 0.34 ng/mL, and CRP 6.4 ng/mL. The patient underwent emergent thromboembolectomy using Fogarty catheters. The embolic material was sent for histological and microbiological examination, both demonstrating presence of fungal infection. Also, blood cultures were positive at this time (<tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Candida">Candida</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="albicans">albicans</tp:taxon-name-part></tp:taxon-name>). To the initial empirical prescription, anidulafungin was added based on the antibiogram. Regarding inflammatory markers</italic>, ﻿<italic>procalcitonin, and WBC fluctuated within a narrow range, whereas CRP showed greater variability. Postoperative course was protracted and complicated, ultimately leading to the patient’s death two months after the operation.</italic></p>
      <fig id="F1" position="float" orientation="portrait">
        <object-id content-type="arpha">4C756D78-B92B-5304-BC85-F6D6419CB787</object-id>
        <label>Figure 1.</label>
        <caption>
          <p>CT angiography revealing infrarenal occlusion of the aorta.</p>
        </caption>
        <graphic xlink:href="foliamedica-67-4-e142295-g001.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1394032.jpg">
          <uri content-type="original_file">https://binary.pensoft.net/fig/1394032</uri>
        </graphic>
      </fig>
      <fig id="F2" position="float" orientation="portrait">
        <object-id content-type="arpha">B0F9DE04-B529-5B78-90DB-9DAF1A7558CC</object-id>
        <label>Figure 2.</label>
        <caption>
          <p>Echochardiography revealing a mobile echogenic mass in the posterior glottis of mitral valve.</p>
        </caption>
        <graphic xlink:href="foliamedica-67-4-e142295-g002.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1394033.jpg">
          <uri content-type="original_file">https://binary.pensoft.net/fig/1394033</uri>
        </graphic>
      </fig>
    </sec>
    <sec sec-type="Discussion" id="SECID0EXAAC">
      <title>Discussion</title>
      <p>Acute aortic occlusion is an uncommon vascular emergency which carries a high degree of morbidity and mortality. It could be the result of acute embolism obstructing the aortic bifurcation or the thrombosis of an existing aortoiliac occlusive disease. Typical symptomatology includes sudden onset of back and lower limb pain, weakness/paralysis and ischemia of both lower extremities. Revascularization options are thromboembolectomy using Fogarty catheters, mechanical thrombectomy with or without stent placement, and axillary-bifemoral bypass.<sup>[<xref ref-type="bibr" rid="B1">1</xref>]</sup> Most significant complications include amputation, renal insufficiency and death. All of the aforementioned outcomes are affected by the level of the aortic occlusion and duration of ischemia.</p>
      <p>Infective endocarditis (<abbrev xlink:title="Infective endocarditis" id="ABBRID0EGBAC">IE</abbrev>) is associated with high morbidity and mortality and clinical presentation is generally highly variable among patients. It may present with an acute, rapidly progressive infection with high fever 38°C, and combination of cardiac and systematic symptoms (dyspnea and chest pain).<sup>[<xref ref-type="bibr" rid="B2">2</xref>]</sup> However, fungal endocarditis, which represents approximately 1%–3% of all <abbrev xlink:title="Infective endocarditis" id="ABBRID0ERBAC">IE</abbrev> cases, has a more insidious clinical presentation with a low-grade or absence of fever, fatigue, and weight loss, which can mislead the initial assessment.<sup>[<xref ref-type="bibr" rid="B3">3</xref>,<xref ref-type="bibr" rid="B4">4</xref>]</sup> Risk factors for developing <abbrev xlink:title="Infective endocarditis" id="ABBRID0EACAC">IE</abbrev> are both cardiac (e.g., valvular heart disease, prosthetic heart valve) and non-cardiac (e.g., immunosuppression, drug abusers). Modified Duke criteria guide physicians to diagnosis; nevertheless, a diagnosis of fungal <abbrev xlink:title="Infective endocarditis" id="ABBRID0EECAC">IE</abbrev> requires a high degree of clinical suspicion. Embolization of vegetations of the valves usually results in widespread end-organ infarcts. Large enough septic emboli to acutely occlude the aorta are, under any circumstances, rare. Blood culture-negative infective endocarditis (<abbrev xlink:title="Blood culture-negative infective endocarditis" id="ABBRID0EICAC">BCNIE</abbrev>) refers to <abbrev xlink:title="Infective endocarditis" id="ABBRID0EMCAC">IE</abbrev> in which no causative microorganism can be grown using the usual blood culture methods. Echocardiography is the first-line diagnostic imaging technique and positive blood cultures remain the cornerstone of <abbrev xlink:title="Infective endocarditis" id="ABBRID0EQCAC">IE</abbrev> diagnosis. Blood cultures identify the responsible microorganism and allows susceptibility testing to determine the definitive therapeutic approach. Blood culture-negative <abbrev xlink:title="Infective endocarditis" id="ABBRID0EUCAC">IE</abbrev> most commonly arises as a consequence of previous antibiotic administration, underlying the importance of performing blood cultures prior to antibiotic therapy, or due to non-bacterial causative microorganisms (fungi) or fastidious bacteria.<sup>[<xref ref-type="bibr" rid="B3">3</xref>]</sup> In this case, the initial diagnosis was considered to be <abbrev xlink:title="Blood culture-negative infective endocarditis" id="ABBRID0E6CAC">BCNIE</abbrev>, and the patient was administered antibiotics empirically. However, one month later and whilst the patient seemed to recover, the aortic embolization occurred. At the time of presentation, blood cultures and samples from clot removal unfolded the presence of fungi. It is also noteworthy that the postoperative trans-esophageal echocardiography did not reveal the presence of vegetation which was initially seen on mitral valve. This led us to the conclusion that the entire vegetation dislodged and resulted in aorta embolization.</p>
      <p>In an interesting systematic review by Slouha et al., the differences among different types of aortic valve replacements were evaluated.<sup>[<xref ref-type="bibr" rid="B5">5</xref>]</sup> Comparing surgical aortic valve replacement and transcatheter aortic valve replacement, both occurred at an average of 2%. However, there is a difference in the time a patient acquires <abbrev xlink:title="Infective endocarditis" id="ABBRID0EMDAC">IE</abbrev> after valve replacement. So, in the case of surgical replacement, the average time is 1540 days, whereas after transcatheter replacement, the average time is 89 days.</p>
      <p>Fungal endocarditis is less common than bacterial endocarditis, but its incidence is increasing, especially after COVID-19 infection. Yassin et al. reported a case with fungal endocarditis 9 months following COVID-19 infection.<sup>[<xref ref-type="bibr" rid="B6">6</xref>]</sup> Its clinical presentation is more insidious; thus, physicians might consider empiric antifungal treatment in certain high-risk situations such as AIDS, cancer, organ transplant patients on immunosuppressive therapy, prosthetic valve endocarditis, intravenous drug users, recurrent endocarditis or prolonged infection, or hospital-acquired endocarditis.</p>
    </sec>
    <sec sec-type="Conclusion" id="SECID0EZDAC">
      <title>Conclusion</title>
      <p>An early diagnosis of infective endocarditis and prolapse of thromboembolic disease may lead to a lower incidence of acute ischemia. In clinical situations where risk factors suggest fungal involvement, physicians should maintain high suspicion for fungal endocarditis in order to initiate early antifungal therapy.</p>
    </sec>
    <sec sec-type="Funding" id="SECID0E5DAC">
      <title>Funding</title>
      <p>The authors have no funding to report.</p>
    </sec>
    <sec sec-type="Competing interests" id="SECID0EDEAC">
      <title>Competing interests</title>
      <p>The authors have declared that no competing interests exist.</p>
    </sec>
    <sec sec-type="Authors contribution" id="SECID0EIEAC">
      <title>Authors contribution</title>
      <p>Concept and design: C.A. and A.P.; analysis and interpretation: C.A., C.G., and A.M.; data collection: A.P., C.G., and K.S.; writing the article: C.A. and A.P.; critical revision of the article: S.A. Final approval of the article: all authors. Overall responsibility: A.M.</p>
    </sec>
  </body>
  <back>
    <ack>
      <title>Acknowledgements</title>
      <p>The authors have no support to report.</p>
    </ack>
    <ref-list>
      <title>References</title>
      <ref id="B1">
        <mixed-citation xlink:type="simple">1. Björck M, Earnshaw JJ, Acosta S, et al. Editor’s choice–European Society for Vascular Surgery (ESVS) 2020 clinical practice guidelines on the management of acute limb ischemia. Eur J Vasc Endovasc Surg 2020; 59(2):173–218.</mixed-citation>
      </ref>
      <ref id="B2">
        <mixed-citation xlink:type="simple">2. Kamde SP, Anjankar A. Pathogenesis, diagnosis, antimicrobial therapy, and management of infective endocarditis, and its complications. Cureus 2022; 14(9):e29 182.</mixed-citation>
      </ref>
      <ref id="B3">
        <mixed-citation xlink:type="simple">3. Thompson GR, Jenks JD, Baddley JW, et al. Fungal endocarditis: pathophysiology, epidemiology, clinical presentation, diagnosis, and management. Clin Microbiol Rev 2023; 36(3):e0001923. doi: <ext-link xlink:type="simple" ext-link-type="doi" xlink:href="10.1128/cmr.00019-23">10.1128/cmr.00019-23</ext-link></mixed-citation>
      </ref>
      <ref id="B4">
        <mixed-citation xlink:type="simple">4. Correia JL, Fiuza JG, Ferreira G, et al. Embolic stroke and misidentification candida species endocarditis: Case presentation and literature review. Diagn Microbiol Infect Dis 2024; 108(2):116133. doi: <ext-link xlink:type="simple" ext-link-type="doi" xlink:href="10.1016/j.diagmicrobio.2023.116133">10.1016/j.diagmicrobio.2023.116133</ext-link></mixed-citation>
      </ref>
      <ref id="B5">
        <mixed-citation xlink:type="simple">5. Slouha E, Rood C, Burle V, et al. Infective endocarditis following aortic valve replacement: a systematic review. Cureus 2023; 15(11):e49048.</mixed-citation>
      </ref>
      <ref id="B6">
        <mixed-citation xlink:type="simple">6. Yassin Z, Hajsadeghi S, Shavazi MT, et al. Endocarditis caused by Aspergillus fumigatus in a patient 9 months after COVID-19 infection recovery: a case report and review of the literature. J Medic Case Rep 2023; 17(1):519.</mixed-citation>
      </ref>
    </ref-list>
  </back>
</article>
