<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.2 20190208//EN" "http://jats.nlm.nih.gov/publishing/1.2/JATS-journalpublishing1.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" article-type="case-report" dtd-version="1.2" xml:lang="en">
    <front>
        <journal-meta>
            <journal-id journal-id-type="pmc">F1000Research</journal-id>
            <journal-title-group>
                <journal-title>F1000Research</journal-title>
            </journal-title-group>
            <issn pub-type="epub">2046-1402</issn>
            <publisher>
                <publisher-name>F1000 Research Limited</publisher-name>
                <publisher-loc>London, UK</publisher-loc>
            </publisher>
        </journal-meta>
        <article-meta>
            <article-id pub-id-type="doi">10.12688/f1000research.23629.1</article-id>
            <article-categories>
                <subj-group subj-group-type="heading">
                    <subject>Case Report</subject>
                </subj-group>
                <subj-group>
                    <subject>Articles</subject>
                </subj-group>
            </article-categories>
            <title-group>
                <article-title>Case Report: Suspected COVID-19 death in the community - histological lung findings and the challenges faced by the pathologist</article-title>
                <fn-group content-type="pub-status">
                    <fn>
                        <p>[version 1; peer review: 1 approved, 1 approved with reservations]</p>
                    </fn>
                </fn-group>
            </title-group>
            <contrib-group>
                <contrib contrib-type="author" corresp="yes">
                    <name>
                        <surname>Jenkins</surname>
                        <given-names>Megan</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Investigation</role>
                    <role content-type="http://credit.niso.org/">Writing &#x2013; Original Draft Preparation</role>
                    <role content-type="http://credit.niso.org/">Writing &#x2013; Review &amp; Editing</role>
                    <uri content-type="orcid">https://orcid.org/0000-0002-5106-8676</uri>
                    <xref ref-type="corresp" rid="c1">a</xref>
                    <xref ref-type="aff" rid="a1">1</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>Johnson</surname>
                        <given-names>Oliver</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Data Curation</role>
                    <role content-type="http://credit.niso.org/">Writing &#x2013; Original Draft Preparation</role>
                    <xref ref-type="aff" rid="a2">2</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>Helliwell</surname>
                        <given-names>Tim</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Supervision</role>
                    <role content-type="http://credit.niso.org/">Writing &#x2013; Review &amp; Editing</role>
                    <xref ref-type="aff" rid="a3">3</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>Johnson</surname>
                        <given-names>Christopher Paul</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Writing &#x2013; Review &amp; Editing</role>
                    <xref ref-type="aff" rid="a1">1</xref>
                </contrib>
                <aff id="a1">
                    <label>1</label>Forensic Pathology Unit, Liverpool University Hospitals NHS Foundation Trust, Liverpool, L7 8XP, UK</aff>
                <aff id="a2">
                    <label>2</label>Dermatology Department, Liverpool University Hospitals NHS Foundation Trust, Liverpool, L7 8XP, UK</aff>
                <aff id="a3">
                    <label>3</label>Cellular Pathology, Liverpool University Hospitals NHS Foundation Trust, Liverpool, L7 8XP, UK</aff>
            </contrib-group>
            <author-notes>
                <corresp id="c1">
                    <label>a</label>
                    <email xlink:href="mailto:megan.jenkins@liverpoolft.nhs.uk">megan.jenkins@liverpoolft.nhs.uk</email>
                </corresp>
                <fn fn-type="conflict">
                    <p>No competing interests were disclosed.</p>
                </fn>
            </author-notes>
            <pub-date pub-type="epub">
                <day>11</day>
                <month>5</month>
                <year>2020</year>
            </pub-date>
            <pub-date pub-type="collection">
                <year>2020</year>
            </pub-date>
            <volume>9</volume>
            <elocation-id>348</elocation-id>
            <history>
                <date date-type="accepted">
                    <day>1</day>
                    <month>5</month>
                    <year>2020</year>
                </date>
            </history>
            <permissions>
                <copyright-statement>Copyright: &#x00a9; 2020 Jenkins M et al.</copyright-statement>
                <copyright-year>2020</copyright-year>
                <license xlink:href="https://creativecommons.org/licenses/by/4.0/">
                    <license-p>This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
                </license>
            </permissions>
            <self-uri content-type="pdf" xlink:href="https://f1000research.com/articles/9-348/pdf"/>
            <abstract>
                <p>Coronavirus disease 2019 (COVID- 19) has now been declared a global pandemic. The literature on the histopathological changes associated with COVID-19 infection is currently limited. Early data consistently describe diffuse alveolar damage on lung histology from patients with COVID-19 pneumonia. We present the case of a 65-year-old female who died whilst self-isolating in the community following a short history of symptoms consistent with COVID-19. An invasive autopsy and subsequent lung histology demonstrated diffuse alveolar damage, in keeping with the previously reported cases of COVID-19 pneumonia. We hope to contribute to the growing body of literature available on the pathological findings in such cases. The challenges of ascertaining post mortem virological confirmation of infection are discussed.</p>
            </abstract>
            <kwd-group kwd-group-type="author">
                <kwd>Coronavirus</kwd>
                <kwd>COVID-19</kwd>
                <kwd>Severe acute respiratory syndrome coronavirus 2</kwd>
                <kwd>Autopsy</kwd>
                <kwd>Diffuse alveolar damage</kwd>
                <kwd>Acute respiratory distress syndrome</kwd>
            </kwd-group>
            <funding-group>
                <funding-statement>The author(s) declared that no grants were involved in supporting this work.</funding-statement>
            </funding-group>
        </article-meta>
    </front>
    <body>
        <sec sec-type="intro">
            <title>Introduction</title>
            <p>Coronavirus disease 2019 (COVID- 19) is a novel coronavirus that has spread rapidly across the globe and on the 12th March 2020, the World Health Organisation declared the outbreak a global pandemic
                <sup>
                    <xref ref-type="bibr" rid="ref-1">1</xref>
                </sup>. The current data suggests the mortality rate from COVID-19 is 2&#x2013;5%
                <sup>
                    <xref ref-type="bibr" rid="ref-2">2</xref>
                </sup>. The spectrum of disease severity varies, with 14% suffering severe disease and 5% experiencing critical disease, defined as respiratory failure with shock or multi-organ dysfunction
                <sup>
                    <xref ref-type="bibr" rid="ref-3">3</xref>
                </sup>. Respiratory failure is often the result of acute respiratory distress syndrome (ARDS)
                <sup>
                    <xref ref-type="bibr" rid="ref-4">4</xref>
                </sup>. The current literature on the histopathological changes associated with COVID-19 infection is limited to ten cases and diffuse alveolar damage (DAD) is consistently reported as the primary abnormality
                <sup>
                    <xref ref-type="bibr" rid="ref-5">5</xref>&#x2013;
                    <xref ref-type="bibr" rid="ref-9">9</xref>
                </sup>.</p>
            <p>We present the case of a 65-year-old female who died in the community amid the COVID-19 pandemic. The aim of this report is contribute to the limited data available on the pathological findings in COVID-19 cases and to highlight the challenge of ascertaining virological PCR confirmation in those patients who have died.</p>
        </sec>
        <sec sec-type="cases">
            <title>Case report</title>
            <p>A 65-year-old Caucasian female cleaner with a background of chronic kidney disease and morbid obesity contacted her GP regarding a short history of dry cough and a sore throat. Her GP prescribed antibiotics and advised the patient to self-isolate in line with the NHS COVID-19 guidance. The following day she was discovered deceased at her home address.</p>
            <p>The Coroner requested a post mortem examination. External examination of the body confirmed morbid obesity (BMI 49.6kg/m
                <sup>2</sup>). There was no evidence of recent injury. On internal examination, the most striking abnormality was the appearance of the lungs, which were heavy (combined weight 1658g) and diffusely firm (
                <xref ref-type="fig" rid="f1">Figure 1</xref>). No pus was expressed from the cut surface. The air passages contained frothy oedema and there was mild reddening of the mucosae. Additionally, there was cardiomegaly (heart weight: 524g) and both ventricles appeared dilated. Scattered, coarse scars were present across the renal surfaces. Internal examination showed no other significant abnormality.</p>
            <fig fig-type="figure" id="f1" orientation="portrait" position="float">
                <label>Figure 1. </label>
                <caption>
                    <p>(
                        <bold>a</bold>) Both lungs were firm and heavy; the left lung weighed 778g and the right lung weighed 880g. (
                        <bold>b</bold>) The cut surface of the lung appeared reddened. There was no consolidation or pus.</p>
                </caption>
                <graphic orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/26074/03f510ed-e95e-431a-bcbd-c9c39dc68c3d_figure1.gif"/>
            </fig>
            <p>Histology of the lungs showed diffuse hyaline membrane formation, typical of DAD. In areas, narrow hyaline membranes lined the alveolar sacs; elsewhere, these changes were more severe (
                <xref ref-type="fig" rid="f2">Figure 2</xref> and 
                <xref ref-type="fig" rid="f3">Figure 3</xref>). There was prominent pulmonary oedema and variable congestion of the alveolar septal capillaries (
                <xref ref-type="fig" rid="f4">Figure 4</xref>). Focally there was an increase in interstitial chronic inflammatory cells and there was type II pneumocyte hyperplasia (
                <xref ref-type="fig" rid="f5">Figure 5</xref> and 
                <xref ref-type="fig" rid="f6">Figure 6</xref>). In areas, the bronchiolar epithelium appeared attenuated with possible ulceration, indicating larger airway involvement (
                <xref ref-type="fig" rid="f7">Figure 7</xref>). No viral inclusion bodies or multinucleated giant cells were seen.</p>
            <fig fig-type="figure" id="f2" orientation="portrait" position="float">
                <label>Figure 2. </label>
                <caption>
                    <p>(
                        <bold>a</bold>) The histologic features showed relatively marked variation; in some areas, the diffuse alveolar damage appears milder. Early hyaline membranes line the alveolar airspaces and ducts. (
                        <bold>b</bold>). Elsewhere, hyaline membranes are broader and more extensive. (&#x00d7;20)</p>
                </caption>
                <graphic orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/26074/03f510ed-e95e-431a-bcbd-c9c39dc68c3d_figure2.gif"/>
            </fig>
            <fig fig-type="figure" id="f3" orientation="portrait" position="float">
                <label>Figure 3. </label>
                <caption>
                    <p>(
                        <bold>a</bold> &amp; 
                        <bold>b</bold>) The hyaline membranes are often regarded as the defining feature of the &#x2018;exudative phase&#x2019; of diffuse alveolar damage. In the airspaces contained necrotic cellular debris and haemorrhagic oedema rich in fibrin due to the damaged alveolar walls. These materials condense to form the hyaline membranes. (x10, &#x00d7;20).</p>
                </caption>
                <graphic orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/26074/03f510ed-e95e-431a-bcbd-c9c39dc68c3d_figure3.gif"/>
            </fig>
            <fig fig-type="figure" id="f4" orientation="portrait" position="float">
                <label>Figure 4. </label>
                <caption>
                    <title>Some areas showed marked oedema and congestion of the intraalveolar capillaries.</title>
                    <p>(x10).</p>
                </caption>
                <graphic orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/26074/03f510ed-e95e-431a-bcbd-c9c39dc68c3d_figure4.gif"/>
            </fig>
            <fig fig-type="figure" id="f5" orientation="portrait" position="float">
                <label>Figure 5. </label>
                <caption>
                    <title>Focally, the interstitium is expanded and infiltrated by chronic inflammatory cells.</title>
                    <p>Very occasional neutrophils are present within the bronchiole walls, but no acute inflammatory cells are seen within the airspaces. Scattered, large cells with multilobed nuclei are present in the alveoli, which likely represent megakaryocytes [not visible at this magnification]. (x10).</p>
                </caption>
                <graphic orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/26074/03f510ed-e95e-431a-bcbd-c9c39dc68c3d_figure5.gif"/>
            </fig>
            <fig fig-type="figure" id="f6" orientation="portrait" position="float">
                <label>Figure 6. </label>
                <caption>
                    <p>(
                        <bold>a</bold> &amp; 
                        <bold>b</bold>) There is hyperplasia of type II pneumocytes and expansion of the alveolar walls due to fibroblast proliferation. (x10, x20).</p>
                </caption>
                <graphic orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/26074/03f510ed-e95e-431a-bcbd-c9c39dc68c3d_figure6.gif"/>
            </fig>
            <fig fig-type="figure" id="f7" orientation="portrait" position="float">
                <label>Figure 7. </label>
                <caption>
                    <p>(
                        <bold>a</bold>) There is widespread loss of the respiratory epithelium, which is likely artefactual and is often seen in post mortem lung histology; however, very occasionally this feature appears genuine. Here, the bronchiole lining appears attenuated and the lumen contained a fibrin plug. (
                        <bold>b</bold>) There is attenuation of the epithelium with focal ulceration (12 to 3 o&#x2019;clock position). The bronchiole wall and surrounding parenchyma are infiltrated by chronic inflammatory cells. (x10).</p>
                </caption>
                <graphic orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/26074/03f510ed-e95e-431a-bcbd-c9c39dc68c3d_figure7.gif"/>
            </fig>
            <p>Histology of the heart, brain, spleen, thyroid and tonsils were normal. Sections taken from the kidneys revealed mild glomerulosclerosis. The liver showed mild fatty change. Unfortunately, in certain parts of the UK, laboratories are not processing virology samples in patients who have already died and therefore virological confirmation was not available. The cause of death was offered as COVID-19 based on the history and histopathological findings.</p>
        </sec>
        <sec sec-type="discussion">
            <title>Discussion</title>
            <p>This case report describes the autopsy findings in an individual who died in the community whilst isolating with symptoms of COVID-19. The current literature on post mortem findings in cases of COVID-19 infection is limited, but the available data consistently highlights DAD as the predominant pathological process. This case report contributes to the growing body of evidence that describes features of DAD in the setting of COVID-19 associated acute respiratory symptoms. There is also emerging evidence to suggest some individuals may develop cardiovascular complications due to COVID-19 infection
                <sup>
                    <xref ref-type="bibr" rid="ref-10">10</xref>&#x2013;
                    <xref ref-type="bibr" rid="ref-12">12</xref>
                </sup>. In this case, the heart was enlarged but histology was normal and these changes most likely represent obesity-related cardiomegaly.</p>
            <p>The absence of post mortem virology testing is a limitation in this case. Considering the consistent symptomology and amidst the current pandemic, the histopathological changes were considered diagnostic for COVID-19. Availability and sensitivity of testing seem varied across the UK. In some regions, autopsy examinations are delayed whilst awaiting results from post mortem nasal swabs; an invasive examination is only carried out if these results are negative. Interestingly, in the recent case published by Barton LM 
                <italic toggle="yes">et al.</italic>,
                <sup>
                    <xref ref-type="bibr" rid="ref-9">9 </xref>
                </sup>nasal swabs were positive for COVID-19 but pulmonary swabs were negative and post mortem examination revealed bronchopneumonia as the cause of death, suggesting post mortem nasopharyngeal swabs may not be an accurate screening method after death. Based on the data available, it appears that lung histology provides the most reliable means to attribute death to COVID-19 infection, providing the clinical history is appropriate. It is worth noting that currently in the UK, suspected COVID cases in the community are not able to access confirmatory swabbing and so the onus will often fall to the pathologists to establish an appropriate cause of death. From anecdotal hospital experience, patients who develop COVID-19 associated ARDS will often succumb rapidly following a dramatic increase in oxygen requirements over a period of several hours (Johnson O, personal communication, 14 Apr 2020). For this reason, the authors are aware that the number of community deaths will inevitably continue to increase given that some patients may not be able to get to secondary care in a timely fashion.</p>
            <p>At our centre, invasive autopsies in cases of suspected COVID-19 infection are now only performed when the history indicates a probable alternative to the cause of death, or where there are concerns that the death may be suspicious. When it seems that death has resulted from respiratory failure, post mortems are limited to an external examination for the purposes of ruling out unnatural causes. Providing there are no unexpected or suspicious findings, a cause of death is offered based on a history consistent with COVID-19 infection. Whilst there are many benefits to an invasive autopsy, such as facilitating accurate diagnosis, excluding internal trauma and improving understanding of the disease, factors such as accessibility of COVID-19 testing, availability of personal protective equipment, infection risk to staff and body storage capacity must be considered. Where COVID-19 is suspected, the appropriateness of performing an invasive procedure must be decided on a case-by-case basis.</p>
        </sec>
        <sec>
            <title>Consent</title>
            <p>Written informed consent for publication of their clinical details and clinical images was obtained from the next of kin of the patient.</p>
        </sec>
        <sec>
            <title>Data availability</title>
            <p>All data underlying the results are available as part of the article and no additional source data are required.</p>
        </sec>
    </body>
    <back>
        <ack>
            <title>Acknowledgements</title>
            <p>The authors would like to thank HM Coroner for the Liverpool and Wirral area for his permission to publish this case. The use of this case is in accordance with the requirements of the Human Tissue Act 2004 (UK).</p>
        </ack>
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    <sub-article article-type="reviewer-report" id="report96474">
        <front-stub>
            <article-id pub-id-type="doi">10.5256/f1000research.26074.r96474</article-id>
            <title-group>
                <article-title>Reviewer response for version 1</article-title>
            </title-group>
            <contrib-group>
                <contrib contrib-type="author">
                    <name>
                        <surname>von der Th&#x00fc;sen</surname>
                        <given-names>Jan H</given-names>
                    </name>
                    <xref ref-type="aff" rid="r96474a1">1</xref>
                    <role>Referee</role>
                    <uri content-type="orcid">https://orcid.org/0000-0001-9699-4860</uri>
                </contrib>
                <aff id="r96474a1">
                    <label>1</label>Department of Pathology, Erasmus University Medical Center, Rotterdam, The Netherlands</aff>
            </contrib-group>
            <author-notes>
                <fn fn-type="conflict">
                    <p>
                        <bold>Competing interests: </bold>No competing interests were disclosed.</p>
                </fn>
            </author-notes>
            <pub-date pub-type="epub">
                <day>25</day>
                <month>10</month>
                <year>2021</year>
            </pub-date>
            <permissions>
                <copyright-statement>Copyright: &#x00a9; 2021 von der Th&#x00fc;sen JH</copyright-statement>
                <copyright-year>2021</copyright-year>
                <license xlink:href="https://creativecommons.org/licenses/by/4.0/">
                    <license-p>This is an open access peer review report distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
                </license>
            </permissions>
            <related-article ext-link-type="doi" id="relatedArticleReport96474" related-article-type="peer-reviewed-article" xlink:href="10.12688/f1000research.23629.1"/>
            <custom-meta-group>
                <custom-meta>
                    <meta-name>recommendation</meta-name>
                    <meta-value>approve-with-reservations</meta-value>
                </custom-meta>
            </custom-meta-group>
        </front-stub>
        <body>
            <p>In the current report, the authors describe their findings regarding the autopsy of a patient suspected for death due to COVID-19. The most important findings are those of DAD in the lungs, which are described in some detail and with appropriate illustrations. This is a not uncommon finding in fatal COVID-19, and they therefore conclude that this is evidence of COVID-19 infection. Unfortunately, DAD is frequently seen in deceased patients, and can have many causes and associations, and the conclusion may be based on over-interpretation. Viral testing may not have been possible at the time, but IHC for SARS-CoV-2 is currently widely available, and could have been applied to this case.&#x00a0;</p>
            <p> </p>
            <p> Also, presently the literature is certainly not limited to 10 cases anymore, and this statement in the introduction should therefore be deleted or altered.</p>
            <p>Are enough details provided of any physical examination and diagnostic tests, treatment given and outcomes?</p>
            <p>Yes</p>
            <p>Is the case presented with sufficient detail to be useful for other practitioners?</p>
            <p>Partly</p>
            <p>Is sufficient discussion included of the importance of the findings and their relevance to future understanding of disease processes, diagnosis or treatment?</p>
            <p>Partly</p>
            <p>Is the background of the case&#x2019;s history and progression described in sufficient detail?</p>
            <p>Yes</p>
            <p>Reviewer Expertise:</p>
            <p>Pulmonary pathology</p>
            <p>I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however I have significant reservations, as outlined above.</p>
        </body>
    </sub-article>
    <sub-article article-type="reviewer-report" id="report63295">
        <front-stub>
            <article-id pub-id-type="doi">10.5256/f1000research.26074.r63295</article-id>
            <title-group>
                <article-title>Reviewer response for version 1</article-title>
            </title-group>
            <contrib-group>
                <contrib contrib-type="author">
                    <name>
                        <surname>Lucas</surname>
                        <given-names>Sebastian</given-names>
                    </name>
                    <xref ref-type="aff" rid="r63295a1">1</xref>
                    <role>Referee</role>
                </contrib>
                <aff id="r63295a1">
                    <label>1</label>Department of Histopathology, KCL School of Medicine, St Thomas&#x2019; Hospital, London, UK</aff>
            </contrib-group>
            <author-notes>
                <fn fn-type="conflict">
                    <p>
                        <bold>Competing interests: </bold>No competing interests were disclosed.</p>
                </fn>
            </author-notes>
            <pub-date pub-type="epub">
                <day>22</day>
                <month>5</month>
                <year>2020</year>
            </pub-date>
            <permissions>
                <copyright-statement>Copyright: &#x00a9; 2020 Lucas S</copyright-statement>
                <copyright-year>2020</copyright-year>
                <license xlink:href="https://creativecommons.org/licenses/by/4.0/">
                    <license-p>This is an open access peer review report distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
                </license>
            </permissions>
            <related-article ext-link-type="doi" id="relatedArticleReport63295" related-article-type="peer-reviewed-article" xlink:href="10.12688/f1000research.23629.1"/>
            <custom-meta-group>
                <custom-meta>
                    <meta-name>recommendation</meta-name>
                    <meta-value>approve</meta-value>
                </custom-meta>
            </custom-meta-group>
        </front-stub>
        <body>
            <p>The case report describes an autopsy of a person who almost certainly died of COVID-19 lung disease, on the basis of the circumstances of death and the lung histology (all other organs were normal for age).</p>
            <p> </p>
            <p> The problems of getting virology tests done on cadavers is addressed - though it should be noted that currently this situation has improved and most mortuaries are now able to access viral tests for COVID-19.</p>
            <p> </p>
            <p> The lung histology is typical for COVID-19 infection and the illustrations are good.</p>
            <p>Are enough details provided of any physical examination and diagnostic tests, treatment given and outcomes?</p>
            <p>Yes</p>
            <p>Is the case presented with sufficient detail to be useful for other practitioners?</p>
            <p>Yes</p>
            <p>Is sufficient discussion included of the importance of the findings and their relevance to future understanding of disease processes, diagnosis or treatment?</p>
            <p>Yes</p>
            <p>Is the background of the case&#x2019;s history and progression described in sufficient detail?</p>
            <p>Yes</p>
            <p>Reviewer Expertise:</p>
            <p>Morbid anatomy and infectious diseases.</p>
            <p>I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.</p>
        </body>
    </sub-article>
</article>
