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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">BR</journal-id>
<journal-title-group>
<journal-title>Biomedical Reports</journal-title>
</journal-title-group>
<issn pub-type="ppub">2049-9434</issn>
<issn pub-type="epub">2049-9442</issn>
<publisher>
<publisher-name>D.A. Spandidos</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">BR-20-5-01771</article-id>
<article-id pub-id-type="doi">10.3892/br.2024.1771</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Case report</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>SARS-CoV-2 associated unilateral parotitis in children: A case report and literature review</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Marino</surname><given-names>Andrea</given-names></name>
<xref rid="af1-BR-20-5-01771" ref-type="aff">1</xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Cacciaguerra</surname><given-names>Giovanni</given-names></name>
<xref rid="af2-BR-20-5-01771" ref-type="aff">2</xref>
<xref rid="c1-BR-20-5-01771" ref-type="corresp"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Spampinato</surname><given-names>Serena</given-names></name>
<xref rid="af1-BR-20-5-01771" ref-type="aff">1</xref>
<xref rid="af3-BR-20-5-01771" ref-type="aff">3</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Palermo</surname><given-names>Monica</given-names></name>
<xref rid="af4-BR-20-5-01771" ref-type="aff">4</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Biasco</surname><given-names>Arturo</given-names></name>
<xref rid="af2-BR-20-5-01771" ref-type="aff">2</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Liotta</surname><given-names>Emanuele</given-names></name>
<xref rid="af2-BR-20-5-01771" ref-type="aff">2</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Cocuzza</surname><given-names>Salvatore</given-names></name>
<xref rid="af5-BR-20-5-01771" ref-type="aff">5</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Venanzi Rullo</surname><given-names>Emmanuele</given-names></name>
<xref rid="af3-BR-20-5-01771" ref-type="aff">3</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Nunnari</surname><given-names>Giuseppe</given-names></name>
<xref rid="af1-BR-20-5-01771" ref-type="aff">1</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Pavone</surname><given-names>Piero</given-names></name>
<xref rid="af2-BR-20-5-01771" ref-type="aff">2</xref>
</contrib>
</contrib-group>
<aff id="af1-BR-20-5-01771"><label>1</label>Department of Clinical and Experimental Medicine, Unit of Infectious Diseases, University of Catania, ARNAS Garibaldi Hospital, I-95122 Catania, Italy</aff>
<aff id="af2-BR-20-5-01771"><label>2</label>Department of Clinical and Experimental Medicine, Section of Paediatrics and Child Neuropsychiatry, School of Specialization in Paediatrics, University of Catania, I-95124 Catania, Italy</aff>
<aff id="af3-BR-20-5-01771"><label>3</label>Department of Clinical and Experimental Medicine, University of Messina, I-98124 Messina, Italy</aff>
<aff id="af4-BR-20-5-01771"><label>4</label>Department of Medical Surgical Sciences and Advanced Technologies &#x2018;GF Ingrassia&#x2019;, Radiology Unit 1, University of Catania, I-95125 Catania, Italy</aff>
<aff id="af5-BR-20-5-01771"><label>5</label>Department of Medical and Surgical Sciences and Advanced Technologies &#x2018;GF Ingrassia&#x2019;, ENT Section, University of Catania, I-95124 Catania, Italy</aff>
<author-notes>
<corresp id="c1-BR-20-5-01771"><italic>Correspondence to:</italic> Dr Giovanni Cacciaguerra, Department of Clinical and Experimental Medicine, Section of Paediatrics and Child Neuropsychiatry, School of Specialization in Paediatrics, University of Catania, Via Santa Sofia 97, I-95124 Catania, Italy <email>fanlin1016@163.com Gio.cacciaguerra@gmail.com </email></corresp>
</author-notes>
<pub-date pub-type="collection">
<month>05</month>
<year>2024</year></pub-date>
<pub-date pub-type="epub">
<day>27</day>
<month>03</month>
<year>2024</year></pub-date>
<volume>20</volume>
<issue>5</issue>
<elocation-id>83</elocation-id>
<history>
<date date-type="received">
<day>24</day>
<month>01</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>14</day>
<month>03</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2024 Marino et al.</copyright-statement>
<copyright-year>2024</copyright-year>
<license license-type="open-access">
<license-p>This is an open access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License</ext-link>, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.</license-p></license>
</permissions>
<abstract>
<p>Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection usually affects the respiratory system; however, a number of atypical manifestations of this disease have also been reported, especially in children. The present study reports a case of a 12-year-old presenting with right unilateral parotitis and sialadenitis and SARS-CoV-2 infection. The young patient, after a 3-day history of fever, was brought to our clinic (Polyclinic University Hospital &#x2018;G. Rodolico&#x2019;, Catania, Italy) for the sudden onset of unilateral parotitis accompanied by sialadenitis and hyperaemia of the skin, which was tender to touch. The SARS-CoV-2 molecular swab was positive; the ultrasound of the affected region showed an increase in the volume of the parotid and sublingual gland and reactive lymph nodes compatible with parotitis and sialadenitis. This case suggests that, in the present Coronavirus disease 2019 pandemic, SARS-CoV-2 should be included in the differential diagnosis of parotitis and sialadenitis along with mumps and flue. Notably, a respiratory panel and serology for other potential causes are needed in case of parotitis-like disease.</p>
</abstract>
<kwd-group>
<kwd>parotitis</kwd>
<kwd>Severe acute respiratory syndrome coronavirus 2 parotitis</kwd>
<kwd>atypical Coronavirus disease 2019</kwd>
<kwd>Coronavirus disease 2019 in children</kwd>
</kwd-group>
<funding-group>
<funding-statement><bold>Funding:</bold> No funding was received.</funding-statement>
</funding-group>
</article-meta>
</front>
<body>
<sec sec-type="intro">
<title>Introduction</title>
<p>SARS-CoV-2, the virus responsible for the global pandemic of Coronavirus Disease 2019 (COVID-19), first identified in Wuhan, China, in December 2019, has led to unprecedented challenges in public health, clinical management and medical research. This coronavirus primarily targets human cells from several tissues by binding to the angiotensin-converting enzyme II (ACE2) receptor (<xref rid="b1-BR-20-5-01771" ref-type="bibr">1</xref>). The virus predominantly spreads through respiratory droplets that are released during activities such as coughing, sneezing or even talking, explaining the high transmissibility and infectious nature of the virus (<xref rid="b2-BR-20-5-01771 b3-BR-20-5-01771 b4-BR-20-5-01771" ref-type="bibr">2-4</xref>).</p>
<p>The clinical spectrum of COVID-19 is remarkably diverse, ranging from asymptomatic or mild flu-like symptoms in &#x007E;70&#x0025; of patients, to severe respiratory distress and multi-organ failure in more critical cases (<xref rid="b2-BR-20-5-01771" ref-type="bibr">2</xref>). Commonly reported symptoms include fever, malaise, dry cough and sore throat. However, the pandemic has unveiled a myriad of atypical presentations that deviate from the classical respiratory symptoms, thereby complicating the diagnostic process (<xref rid="b5-BR-20-5-01771" ref-type="bibr">5</xref>). These atypical manifestations include, but are not limited to, ocular symptoms, cardiac complications such as myocarditis, dermatological signs, gastrointestinal and hepatic disturbances, cerebrovascular incidents and various neurological symptoms (<xref rid="b6-BR-20-5-01771" ref-type="bibr">6</xref>).</p>
<p>The recognition of these unusual presentations is pivotal in ensuring timely diagnosis and appropriate management of COVID-19. Such awareness also aids in implementing effective isolation measures to curtail the spread of SARS-CoV-2. Among these atypical manifestations, oral symptoms have garnered attention, ranging from simple taste disturbances to more complex conditions such as mucosal lesions and salivary gland infections (<xref rid="b7-BR-20-5-01771" ref-type="bibr">7</xref>).</p>
<p>The impact of SARS-CoV-2 on children, although initially perceived as minor, has evolved into a subject of major concern. In paediatric patients, the virus often manifests in forms markedly different from adults (from asymptomatic diseases, which represent the most common form, to multisystem inflammatory syndrome), which can lead to underdiagnosis or misdiagnosis. This is particularly crucial as children, being active social agents in schools and family units, can be key vectors in the transmission of the virus. Furthermore, the emergence of multisystem inflammatory syndrome in children associated with COVID-19 underscores the unpredictable nature of the virus in the younger population (<xref rid="b8-BR-20-5-01771" ref-type="bibr">8</xref>). Atypical manifestations in children can be more cumbersome than those involving adults, resulting in differential diagnosis and clinical management that may pose challenges for clinicians (<xref rid="b9-BR-20-5-01771" ref-type="bibr">9</xref>).</p>
<p>As such, expanding our knowledge on the diverse clinical presentations of COVID-19 in children, such as the case of SARS-CoV-2 induced parotitis presented in the present case, is not only pivotal for the paediatric care but also for the broader public health strategy. This case report aims to shed light on the less explored aspects of COVID-19 in paediatrics, illustrating how even non-respiratory symptoms can herald the presence of the virus in this demographic, thus necessitating a broader clinical vigilance among healthcare providers.</p>
<p>The present case report contributed to this growing body of literature by reporting SARS-CoV-2 infection presenting primarily with unilateral parotitis and sialadenitis in a 12-year-old girl, further expanding our understanding of the virus&#x0027;s clinical heterogeneity.</p>
</sec>
<sec sec-type="Case|report">
<title>Case report</title>
<p>In November 2023, a 12-year-old female patient visited our clinic (Polyclinic University Hospital &#x2018;G. Rodolico&#x2019;, Catania, Italy) due to the sudden onset of right-sided unilateral parotitis, accompanied by sialadenitis, hyperaemia of the skin and pain upon touch. She was up-to-date on her immunizations, including the measles-mumps-rubella vaccine. The patient had not previously been vaccinated for SARS-CoV-2. The parents of the patient reported no history of taking medications such as propylthiouracil, phenothiazines, iodides or phenylbutazone. The patient had no chronic diseases. Upon admission, her temperature was 36.3&#x02DA;C, heart rate was 78 beats per minute, blood pressure was 110/69 mmHg and oxygen saturation in room air was 99&#x0025;. The parents of the patient reported intermittent fevers (up to 38&#x02DA;C) for 3 days prior to admission without respiratory symptoms or facial swelling. Fever was treated with paracetamol.</p>
<p>Clinical examination was normal for the age and sex of the patient. Blood tests revealed in range haemoglobin and platelet counts. The total white count was 8,440 cells/ml, with neutrophils at 6,380 cells/ml (75.6&#x0025;) and lymphocytes at 1,588 cells/ml (18.8&#x0025;). C-reactive protein levels were raised (15 mg/dl; normal range, 0-0.5 mg/dl) as well as erythrocyte sedimentation rate (47 mm/h; normal range, &#x003C;10 mm/h), ferritin and lactate dehydrogenase levels were within the normal range.</p>
<p>Mumps serology was negative for IgM and positive for IgG. The main viral infectious disease screenings, including serology and a respiratory panel on a pharyngeal swab (BioFire<sup>&#x00AE;</sup> Respiratory 2.1 Panel; BioFire Diagnostics, Inc.; bioM&#x00E9;rieux), were negative. This included tests for Epstein-Barr virus, human herpesvirus 6, human immunodeficiency virus, respiratory syncytial virus, parainfluenza virus types 2 and 3, influenza A and B viruses, adenovirus, coxsackie viruses, parvovirus B19, lymphocytic choriomeningitis virus, human bocavirus and paramyxovirus RNA. Overall, two sets of blood cultures were negative. A nasopharyngeal swab tested positive for SARS-CoV-2, which was subsequently confirmed by the BioFire<sup>&#x00AE;</sup> respiratory panel. A chest radiograph showed no parenchymal lung alterations suggestive of a pneumonic process. The patient had no upper or lower respiratory symptoms.</p>
<p>Ultrasound examination revealed an enlarged right parotid gland and right submandibular gland, both with a homogeneous echostructure and a diffused increase in echogenicity of the glandular parenchyma. There was also a diffuse increase in intraparenchymal vascularity and reactive adenitis. No fluid collection, obstructing stones, dilatation of salivary ducts, masses or abscesses were observed (<xref rid="f1-BR-20-5-01771" ref-type="fig">Fig. 1A</xref> and <xref rid="f1-BR-20-5-01771" ref-type="fig">B</xref>).</p>
<p>Non-steroidal anti-inflammatory drugs therapy (NSAID) with ibuprofen was started at a dosage of 200 mg every 12 h. Although clinical symptoms did not significantly improve, within 48 h clear saliva without pus was observed to discharge from the parotid glands. The patient was discharged with a prescription for analgesic therapy to be used as needed. SARS-CoV-2 swab tested negative after 7 days and the patient did not develop other symptoms or manifestations. Parents reported they administered ibuprofen for a total of 6 days.</p>
<p>At a follow-up visit 2 weeks later, we noted the complete resolution of the clinical condition of the patient.</p>
</sec>
<sec sec-type="Discussion">
<title>Discussion</title>
<p>The present case highlights the novelty of SARS-CoV-2-associated unilateral parotitis in a 12-year-old girl, a rare presentation within the paediatric population. Diverging from typical respiratory symptoms of COVID-19, this instance emphasizes the capability of the virus to cause glandular manifestations such as parotitis. The effective management with NSAIDs, without preceding respiratory symptoms or common viral infections, underscores the importance of considering COVID-19 in differential diagnoses for acute parotitis in children, expanding our understanding of the virus&#x0027;s diverse clinical manifestations.</p>
<p>Similar cases have emerged in the literature since the onset of the COVID-19 pandemic, predominantly in adult populations (<xref rid="b10-BR-20-5-01771 b11-BR-20-5-01771 b12-BR-20-5-01771" ref-type="bibr">10-12</xref>). The clinical spectrum of SARS-CoV-2 infection typically ranges from minimally symptomatic disease to severe pneumonia and critical illness, with &#x007E;70&#x0025; of patients either asymptomatic or exhibiting mild flu-like symptoms, such as fever, dry cough and sore throat (<xref rid="b9-BR-20-5-01771" ref-type="bibr">9</xref>).</p>
<p>The atypical presentations of SARS-CoV-2 infection are diverse, including myocarditis, stroke, liver damage, gastrointestinal symptoms, ocular manifestations, dermatological lesions and a range of neurological symptoms, observed in both mild and severe cases (<xref rid="b13-BR-20-5-01771" ref-type="bibr">13</xref>).</p>
<p>The parotitis seen in SARS-CoV-2 infections can be attributed to several interacting pathological mechanisms (<xref rid="b11-BR-20-5-01771" ref-type="bibr">11</xref>,<xref rid="b12-BR-20-5-01771" ref-type="bibr">12</xref>). Direct viral invasion is a primary suspect, where SARS-CoV-2 infiltrates the salivary gland epithelium by binding to ACE2 receptors, causing local inflammation and cellular damage (<xref rid="b14-BR-20-5-01771" ref-type="bibr">14</xref>). Concurrently, the host&#x0027;s immune response, while attempting to combat the virus, may overshoot, releasing a deluge of cytokines in a detrimental &#x2018;cytokine storm&#x2019;, leading to further tissue inflammation and gland swelling (<xref rid="b15-BR-20-5-01771" ref-type="bibr">15</xref>,<xref rid="b16-BR-20-5-01771" ref-type="bibr">16</xref>). Compounding this, SARS-CoV-2 affects endothelial cells, causing dysfunction that manifests as increased vascular permeability and oedema, which is a condition conducive to parotitis (<xref rid="b17-BR-20-5-01771" ref-type="bibr">17</xref>). The propensity of the virus to induce a hypercoagulable state could also precipitate microthrombi within the tiny blood vessels of the salivary glands, impairing blood flow and oxygen delivery, exacerbating inflammation (<xref rid="b18-BR-20-5-01771" ref-type="bibr">18</xref>). Moreover, the concept of molecular mimicry may offer insight into prolonged or recurrent gland inflammation, as the immune system&#x0027;s production of antibodies against the virus could inadvertently target structurally similar antigens within the salivary glands (<xref rid="b19-BR-20-5-01771" ref-type="bibr">19</xref>). This complex interplay of direct viral effects, immune response dysregulation, vascular pathology and autoimmune phenomena not only elucidates the occurrence of parotitis in COVID-19 but also reflects the multisystemic impact of SARS-CoV-2, warranting a broad spectrum of considerations in the clinical management of these patients (<xref rid="b2-BR-20-5-01771" ref-type="bibr">2</xref>,<xref rid="b20-BR-20-5-01771" ref-type="bibr">20</xref>,<xref rid="b21-BR-20-5-01771" ref-type="bibr">21</xref>).</p>
<p>The timeline for the development of parotitis during SARS-CoV-2 infection is not well-defined. In several reports, parotitis was noted 1-3 days after the onset of coronavirus symptoms (<xref rid="b11-BR-20-5-01771" ref-type="bibr">11</xref>,<xref rid="b22-BR-20-5-01771" ref-type="bibr">22</xref>,<xref rid="b23-BR-20-5-01771" ref-type="bibr">23</xref>). Parotitis not related to mumps has been associated with various viruses, including enteroviruses, adenoviruses, cytomegalovirus, influenza, parainfluenza, Epstein-Barr, herpes simplex and herpes virus 6(<xref rid="b24-BR-20-5-01771" ref-type="bibr">24</xref>).</p>
<p>In the present case, the patient presented with acute mumps-like symptoms and unilateral sialadenitis following a 3-day history of fever, without any chronic diseases, trauma and with normal blood tests. The positive SARS-CoV-2 swab, combined with ultrasound findings which ruled out oncological or obstructive conditions, along with normal blood samples and physical examination, facilitated a non-invasive approach. This approach allowed us to reassure the parents and monitor the patient over time, avoiding the immediate use of more invasive imaging techniques such as CT scans, which involve ionizing radiation.</p>
<p>To the best of our knowledge the scientific literature report before the present study reports only six patients who developed a parotitis which could be ascribed to SARS-CoV-2 infection (<xref rid="tI-BR-20-5-01771" ref-type="table">Table I</xref>). The age of the patient in the present case is somewhat aligned with the range observed in the literature, with reported cases varying from 2 months to 7 years of age (<xref rid="b25-BR-20-5-01771" ref-type="bibr">25</xref>,<xref rid="b26-BR-20-5-01771" ref-type="bibr">26</xref>). While most cases involved males, the present patient is female, suggesting no strong sex predilection for SARS-CoV-2 associated parotitis.</p>
<p>Unlike other cases, the present patient had no preceding respiratory symptoms, which is atypical given that respiratory symptoms were present in most literature cases, albeit mild in some (<xref rid="b27-BR-20-5-01771" ref-type="bibr">27</xref>), highlighting the variable presentation of the disease. All patients had undergone neck ultrasounds. The laboratory parameters in the current case were mostly within normal ranges, contrasting with other reports where leucocytosis and elevated acute-phase reactants were common (<xref rid="b28-BR-20-5-01771" ref-type="bibr">28</xref>). This discrepancy may point to a less aggressive inflammatory response in the present patient.</p>
<p>Our patient was treated only with NSAID therapy, without the need of either antibiotics (often overprescribed by clinicians aiming to prevent bacterial superinfections) or corticosteroid therapy.</p>
<p>The pathogenesis of SARS-CoV-2-associated sialadenitis is yet to be fully understood. However, SARS-CoV-2 should be considered in the differential diagnosis of parotitis/sialadenitis, particularly if it presents unilaterally. Prompt isolation measures are crucial to mitigate the spread of infection (<xref rid="b29-BR-20-5-01771" ref-type="bibr">29</xref>).</p>
<p>The epidemiological landscape of COVID-19 in the paediatric population presents a multifaceted challenge. Although children account for a significant portion of total cases, their clinical manifestations often differ from adults, leading to unique considerations in public health strategies (<xref rid="b30-BR-20-5-01771" ref-type="bibr">30</xref>). Notably, the prevalence of COVID-19 among children varies with age, showing higher incidence in school-aged children and adolescents compared with younger children (<xref rid="b31-BR-20-5-01771" ref-type="bibr">31</xref>,<xref rid="b32-BR-20-5-01771" ref-type="bibr">32</xref>). Additionally, the impact of socioeconomic factors is pronounced in this demographic, as children from lower socioeconomic backgrounds face increased exposure risks and potential health disparities (<xref rid="b33-BR-20-5-01771" ref-type="bibr">33</xref>). Understanding these dynamics is crucial, not only for direct paediatric care but also for broader community health policies, especially considering the role of children in viral transmission within schools and households (<xref rid="b34-BR-20-5-01771" ref-type="bibr">34</xref>). This complex epidemiological profile underscores the need for tailored approaches in both prevention and treatment strategies for COVID-19 among children.</p>
<p>The present case underscores the importance of including SARS-CoV-2, and coronaviruses in general, in the list of pathogens responsible for parotitis and sialadenitis, alongside mumps and influenza. Notably, a comprehensive respiratory panel and serology are essential for accurate diagnosis in cases presenting with parotitis-like symptoms.</p>
<p>Effective COVID-19 prevention in children hinges on a multi-faceted approach that balances public health guidelines with the unique needs of the paediatric population. Vaccination, when available and approved for specific age groups, plays a crucial role in reducing transmission and severity of the disease among children (<xref rid="b35-BR-20-5-01771" ref-type="bibr">35</xref>).</p>
<p>In conclusion, the present case highlights the need for heightened vigilance and a broader diagnostic perspective during the ongoing COVID-19 pandemic. Understanding the diverse clinical manifestations of SARS-CoV-2, including rare presentations such as unilateral parotitis, is crucial for prompt diagnosis, effective patient management and prevention of virus transmission.</p>
</sec>
</body>
<back>
<ack>
<title>Acknowledgements</title>
<p>Not applicable.</p>
</ack>
<sec sec-type="data-availability">
<title>Availability of data and materials</title>
<p>Data sharing is not applicable to this article as no datasets were generated or analysed during the current study.</p>
</sec>
<sec>
<title>Authors&#x0027; contributions</title>
<p>AM, GC, SS, MP, AB, EL, SC, EVR, GN and PP contributed to the study conception and design. GC and AM conceptualised the study. SS designed the methodology. MP, AB, EL and SC performed the investigation. EVR and GN wrote the original draft preparation. GN reviewed and edited the manuscript. PP supervised the study. All authors have read and approved the final manuscript. GN and PP confirm the authenticity of all the raw data.</p>
</sec>
<sec>
<title>Ethics approval and consent to participate</title>
<p>Written informed consent for data collection was obtained from the parents of the subject involved in the study.</p>
</sec>
<sec>
<title>Patient consent for publication</title>
<p>Informed consent for publication was obtained from the parents of the subject involved in the study.</p>
</sec>
<sec sec-type="COI-statement">
<title>Competing interests</title>
<p>The authors declare that they have no competing interests.</p>
</sec>
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</back>
<floats-group>
<fig id="f1-BR-20-5-01771" position="float">
<label>Figure 1</label>
<caption><p>(A) Ultrasound and (B) Ecocolor-Doppler examination of the right parotid gland.</p></caption>
<graphic xlink:href="br-20-05-01771-g00.tif" />
</fig>
<table-wrap id="tI-BR-20-5-01771" position="float">
<label>Table I</label>
<caption><p>Characteristics of SARS-CoV-2 associated parotitis in children.</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="middle">Author</th>
<th align="center" valign="middle">No. of patients</th>
<th align="center" valign="middle">Age</th>
<th align="center" valign="middle">Sex</th>
<th align="center" valign="middle">Symptoms</th>
<th align="center" valign="middle">Lab findings</th>
<th align="center" valign="middle">SARS-CoV-2 test performed</th>
<th align="center" valign="middle">Respiratory symptoms</th>
<th align="center" valign="middle">Treatment</th>
<th align="center" valign="middle">Duration (days)</th>
<th align="center" valign="middle">Outcome</th>
<th align="center" valign="middle">(Refs.)</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">Brehm <italic>et al</italic></td>
<td align="center" valign="middle">1</td>
<td align="left" valign="middle">10 weeks</td>
<td align="center" valign="middle">M</td>
<td align="left" valign="middle">Facial swelling, decreased appetite</td>
<td align="left" valign="middle">Leucocytosis, high platelets</td>
<td align="center" valign="middle">PCR</td>
<td align="left" valign="middle">Rhinorrhoea, cough</td>
<td align="left" valign="middle">Amoxicillin/clavulanic acid</td>
<td align="center" valign="middle">7</td>
<td align="left" valign="middle">Resolved</td>
<td align="center" valign="middle">(<xref rid="b27-BR-20-5-01771" ref-type="bibr">27</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Likitnukul</td>
<td align="center" valign="middle">1</td>
<td align="left" valign="middle">4 years</td>
<td align="center" valign="middle">M</td>
<td align="left" valign="middle">Facial swelling, low grade fever, decreased appetite</td>
<td align="left" valign="middle">High CRP, high amylase</td>
<td align="center" valign="middle">PCR</td>
<td align="left" valign="middle">Mild cough</td>
<td align="left" valign="middle">Analgesic (not specified)</td>
<td align="center" valign="middle">3</td>
<td align="left" valign="middle">Resolved</td>
<td align="center" valign="middle">(<xref rid="b28-BR-20-5-01771" ref-type="bibr">28</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Keles <italic>et al</italic></td>
<td align="center" valign="middle">1</td>
<td align="left" valign="middle">4 years</td>
<td align="center" valign="middle">M</td>
<td align="left" valign="middle">Facial swelling and pain, difficulty swallowing</td>
<td align="left" valign="middle">High amylase</td>
<td align="center" valign="middle">PCR</td>
<td align="left" valign="middle">None</td>
<td align="left" valign="middle">NSAID (not specified)</td>
<td align="center" valign="middle">3</td>
<td align="left" valign="middle">Resolved</td>
<td align="center" valign="middle">(<xref rid="b26-BR-20-5-01771" ref-type="bibr">26</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Sharma <italic>et al</italic></td>
<td align="center" valign="middle">3</td>
<td align="left" valign="middle">7 years</td>
<td align="center" valign="middle">F</td>
<td align="left" valign="middle">Facial swelling, partial maloc- clusion, trismus, decreased appetite</td>
<td align="left" valign="middle">High CRP and ESR, high amylase</td>
<td align="center" valign="middle">PCR</td>
<td align="left" valign="middle">Cough (4 weeks before)</td>
<td align="left" valign="middle">Prednisolone 1 mg/kg/day</td>
<td align="center" valign="middle">5</td>
<td align="left" valign="middle">Resolved</td>
<td align="center" valign="middle">(<xref rid="b25-BR-20-5-01771" ref-type="bibr">25</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;</td>
<td align="center" valign="middle">&#x00A0;</td>
<td align="left" valign="middle">3.5 years</td>
<td align="center" valign="middle">M</td>
<td align="left" valign="middle">Facial swelling, fever, poor appetite</td>
<td align="left" valign="middle">Leucocytosis, high ESR and CRP</td>
<td align="center" valign="middle">PCR</td>
<td align="left" valign="middle">None</td>
<td align="left" valign="middle">Prednisolone 1 mg/kg/day</td>
<td align="center" valign="middle">5</td>
<td align="left" valign="middle">Resolved</td>
<td align="center" valign="middle">&#x00A0;</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;</td>
<td align="center" valign="middle">&#x00A0;</td>
<td align="left" valign="middle">2 months</td>
<td align="center" valign="middle">M</td>
<td align="left" valign="middle">Facial swelling, irritability, decreased appetite, fever</td>
<td align="left" valign="middle">Leucocytosis, high CRP</td>
<td align="center" valign="middle">PCR</td>
<td align="left" valign="middle">None</td>
<td align="left" valign="middle">Metilpredni- solone 2 mg/kg/day</td>
<td align="center" valign="middle">5</td>
<td align="left" valign="middle">Resolved</td>
<td align="center" valign="middle">&#x00A0;</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn><p>SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; CRP, C reactive protein; NSAID, non-steroidal anti-inflammatory drugs; ESR, erythrocyte sedimentation rate.</p></fn>
</table-wrap-foot>
</table-wrap>
</floats-group>
</article>
