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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Pediatr.</journal-id>
<journal-title>Frontiers in Pediatrics</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Pediatr.</abbrev-journal-title>
<issn pub-type="epub">2296-2360</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fped.2023.1143262</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Pediatrics</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Pediatric paragonimiasis: a retrospective analysis of cases from a county in south-west China</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author"><name><surname>Jiang</surname><given-names>Yong-xin</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib>
<contrib contrib-type="author"><name><surname>Li</surname><given-names>Gong-qiang</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib>
<contrib contrib-type="author"><name><surname>Pan</surname><given-names>Cheng-jing</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib>
<contrib contrib-type="author"><name><surname>He</surname><given-names>Zhong-qiu</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib>
<contrib contrib-type="author"><name><surname>Wang</surname><given-names>Chao</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib>
<contrib contrib-type="author"><name><surname>Mu</surname><given-names>Qi-ru</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib>
<contrib contrib-type="author" corresp="yes"><name><surname>Cao</surname><given-names>Lu-lu</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="corresp" rid="cor1">&#x002A;</xref><uri xlink:href="https://loop.frontiersin.org/people/2166657/overview"/></contrib>
</contrib-group>
<aff id="aff1"><label><sup>1</sup></label><addr-line>Department of Pediatrics</addr-line>, <institution>Yanjin Country People&#x2019;s Hospital</institution>, <addr-line>Zhaotong</addr-line>, <country>China</country></aff>
<aff id="aff2"><label><sup>2</sup></label><addr-line>Department of Pediatric Intensive Care Unit</addr-line>, <institution>Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine</institution>, <addr-line>Shanghai</addr-line>, <country>China</country></aff>
<author-notes>
<fn fn-type="edited-by"><p><bold>Edited by:</bold> Azar Shokri, North Khorasan University of Medical Sciences, Iran</p></fn>
<fn fn-type="edited-by"><p><bold>Reviewed by:</bold> Sachin Gajanan Damke, Shri Shankaracharya Institute of Medical Science, India Emmanuel Ekanem, University of Calabar, Nigeria Azadeh Mizani, Pasteur Institute of Iran (PII), Iran</p></fn>
<corresp id="cor1"><label>&#x002A;</label><bold>Correspondence:</bold> Lu-lu Cao <email>caolulu0813@163.com</email>; <email>caolulu@xinhuamed.com.cn</email></corresp>
</author-notes>
<pub-date pub-type="epub"><day>17</day><month>05</month><year>2023</year></pub-date>
<pub-date pub-type="collection"><year>2023</year></pub-date>
<volume>11</volume><elocation-id>1143262</elocation-id>
<history>
<date date-type="received"><day>12</day><month>01</month><year>2023</year></date>
<date date-type="accepted"><day>04</day><month>04</month><year>2023</year></date>
</history>
<permissions>
<copyright-statement>&#x00A9; 2023 Jiang, Li, Pan, He, Wang, Mu and Cao.</copyright-statement>
<copyright-year>2023</copyright-year><copyright-holder>Jiang, Li, Pan, He, Wang, Mu and Cao</copyright-holder><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License (CC BY)</ext-link>. The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p></license>
</permissions>
<abstract>
<sec><title>Introduction</title>
<p>The clinical manifestations of paragonimiasis are diverse and non-specific, and can easily lead to misdiagnosis. We aimed to analyze the clinical manifestations, laboratory features, treatment, and clinical outcome of children with paragonimiasis in order to improve recognition of this disease and avoid misdiagnosis.</p>
</sec>
<sec><title>Methods</title>
<p>Children diagnosed with paragonimiasis from August 2016 to July 2022 were included in the study. Information on population informatics, medical history, and laboratory features was extracted from case data. The clinical features of paragonimiasis were retrospectively analyzed.</p>
</sec>
<sec><title>Results</title>
<p>A total of 45 children were included in this study. All children had, at least, one risk factor. The clinical features mainly included fever, cough, pleural effusion, peritoneal effusion, and subcutaneous nodules. The main imaging findings were alveolar exudation, peritoneal effusion, pleural thickening, and local nodules. The &#x201C;tunnel sign&#x201D; finding on computed tomography (CT)/magnetic resonance imaging (MRI) was helpful in establishing the diagnosis of paragonimiasis. After praziquantel treatment, most of the children improved, and one child with cerebral paragonimiasis experienced sequelae.</p>
</sec>
<sec><title>Conclusion</title>
<p>Most children with paragonimiasis have a good prognosis, but few children can experience sequelae. Avoidance of untreated water and raw food is a simple, feasible, and effective preventive measure.</p>
</sec>
</abstract>
<kwd-group>
<kwd>paragonimiasis</kwd>
<kwd>children</kwd>
<kwd>pleural effusion</kwd>
<kwd>peritoneal effusion</kwd>
<kwd>pericardial effusion</kwd>
</kwd-group>
<counts>
<fig-count count="3"/>
<table-count count="2"/><equation-count count="0"/><ref-count count="16"/><page-count count="0"/><word-count count="0"/></counts><custom-meta-wrap><custom-meta><meta-name>section-at-acceptance</meta-name><meta-value>Pediatric Infectious Diseases</meta-value></custom-meta></custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1" sec-type="intro"><label>1.</label><title>Introduction</title>
<p>Paragonimiasis is an important food-borne parasitic zoonosis caused by <italic>Paragonimus spp</italic> (<xref ref-type="bibr" rid="B1">1</xref>). It was estimated that there were about 23.2 million cases of paragonimiasis worldwide in 2005, including about 5 million heavily infected patients and cases that resulted in death (<xref ref-type="bibr" rid="B2">2</xref>, <xref ref-type="bibr" rid="B3">3</xref>). In China, the national survey from 2001 to 2005 showed that the positive rate of serological tests for <italic>Paragonimus</italic> infection was 1.71&#x0025;, and the positive rate of serological tests was higher in children under 9 years of age (<xref ref-type="bibr" rid="B4">4</xref>). Also, the prevalence of paragonimiasis was higher in Sichuan, Yunnan, and Chongqing due to their special dietary habits (<xref ref-type="bibr" rid="B5">5</xref>).</p>
<p>Human paragonimiasis is usually caused by drinking water containing metacercariae or consumption of raw or uncooked food contaminated with <italic>Paragonimus spp</italic> (<xref ref-type="bibr" rid="B1">1</xref>). There are more than 50 species of <italic>Paragonimus spp</italic>. In China, the main species are <italic>Paragonimus westermani</italic> and <italic>Paragonimus</italic> <italic>skrjabini</italic> (<xref ref-type="bibr" rid="B6">6</xref>). <italic>Paragonimus skrjabini</italic> and <italic>Paragonimus</italic> <italic>westermani</italic> have a similar life cycle.</p>
<fig id="F1" position="float"><label>Figure 1</label>
<caption><p>A 5-year-old boy had habit of drinking untreated water. CT of the lungs showed cystic areas (<bold>A</bold>), pulmonary exudation (<bold>B</bold>) and pleural effusion (<bold>C</bold>).</p></caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="fped-11-1143262-g001.tif"/>
</fig>
<p>Paragonimiasis is still one of the diseases that affect the health of children, especially in southwest China. The nonspecificity of clinical features can easily result in this disease condition being misdiagnosed as other diseases, such as tuberculosis and cancer (<xref ref-type="bibr" rid="B2">2</xref>, <xref ref-type="bibr" rid="B3">3</xref>), especially in a situation in which the medical personnel do not have enough knowledge about the disease or do not pay enough attention to it. This can lead to delayed treatment and even a poor prognosis, as well as an increased medical burden. Thus, the aim of this retrospective study was to improve the recognition of paragonimiasis and reduce misdiagnosis, by analyzing the clinical manifestations, laboratory features, treatment, and prognosis of children with paragonimiasis during the past six years.</p>
</sec>
<sec id="s2"><label>2.</label><title>Materials and methods</title>
<sec id="s2a"><label>2.1.</label><title>Diagnosis of paragonimiasis</title>
<p>The diagnostic criteria were in accordance with the &#x201C;Diagnosis of Paragonimiasis&#x201D; (NO. WS 380-2012), which was drafted by the National Health Commission of the People&#x0027;s Republic of China in 2012 (<xref ref-type="bibr" rid="B6">6</xref>). In brief, the diagnosis of paragonimiasis was based on the risk factor, clinical manifestations, laboratory examination, and imaging examination. Suspected cases were defined as those having clinical features, risk factors and significantly elevated peripheral blood eosinophil ratios or absolute values.</p>
<p>Clinically diagnosed cases were defined as suspected cases that had one of following positive test results: (1) a positive intradermal test; (2) positive serum immunology test; (3) abnormal findings in imaging examination; and (4) biopsy showing characteristic pathological changes. Cases were defined as confirmed cases if <italic>Paragonimus</italic> eggs were found in the sputum or stool, or if <italic>Paragonimus</italic> worms or eggs were found in a subcutaneous mass or other living tissue and body fluids.</p>
<sec id="s2a1"><label>2.1.1.</label><title>Clinical classification of paragonimiasis</title>
<p>The clinical classification was divided into thoracopulmonary paragonimiasis and extrapulmonary paragonimiasis. Patients with thoracopulmonary paragonimiasis may present with cough, chest pain, rusty or blood-stained sputum, pleural lesions, and other symptoms and signs. Patients with extrapulmonary paragonimiasis may have a subcutaneous mass, abdominal discomfort, and abnormal symptoms and signs of the nervous system. Some mildly infected patients may have no obvious clinical symptoms and signs.</p>
</sec>
<sec id="s2a2"><label>2.1.2.</label><title>Risk factors</title>
<p>The risk factor extracted the following: (1) previous history of consumption of raw or semi-raw freshwater crabs and crayfish contaminated with <italic>Paragonimus</italic>, (2) history of consumption of raw or semi-raw mammalian meat (e.g., boar meat and spiny frog), and (3) history of drinking raw or untreated stream water.</p>
</sec>
</sec>
<sec id="s2b"><label>2.2.</label><title>Study population and data collection</title>
<p>From August 2016 to July 2022, 45 children with paragonimiasis infection were admitted to the department of pediatrics, Yanjin County People&#x0027;s Hospital, which is located in a mountainous county with multi-ethnic communities in southwest China. Firstly, patients diagnosed with paragonimiasis, pleural effusion, peritoneal effusion, and pericardial effusion were selected from the case system. Secondly, children with paragonimiasis whose etiological test results were positive for the antibody to <italic>Paragonimiasis</italic> (ELISA, Novo medical, Co. LTD) or in whom eggs/bodies were detected in the tissue were included in this analysis. Then, case data were collected, including blood routine tests (white blood cell count, eosinophilic percentage, hemoglobin concentration, and platelet count) and erythrocyte sedimentation rate (ESR), computed tomography (CT) or x-ray or magnetic resonance imaging (MRI) examination, and cardiac ultrasound and chest ultrasound. Finally, the following examination data were checked to ensure whether there is any misdiagnosis experience: all children with fever and cough were examined for tuberculous bacteria. Participants with pleural, pericardial and peritoneal effusion underwent puncture. Routine, biochemical, and etiological tests for puncture fluid were performed to exclude other pathogens and tumors.</p>
</sec>
<sec id="s2c"><label>2.3.</label><title>Statistical methods</title>
<p>SPSS 22.0 was used for statistical analysis. The median was used for continuous variables because of the skewed distribution of data. Proportion (&#x0025;) was selected for description of categorical variables.</p>
</sec>
<sec id="s2d"><label>2.4.</label><title>Ethics approval and informed consent</title>
<p>Ethical approval for this study was obtained from the Ethics Committee of Xinhua Hospital affiliated to Shanghai Jiao Tong University School of Medicine (NO. XHEC-D-2022-247). As this was a retrospective study, the requirement of obtaining informed consent was waived.</p>
</sec>
</sec>
<sec id="s3" sec-type="results"><label>3.</label><title>Results</title>
<sec id="s3a"><label>3.1.</label><title>Patient demographics and clinical manifestations</title>
<p>A total of 45 children diagnosed with paragonimiasis infection were included in this study. The median age of these children was 96 months (minimum age of 18 months, and maximum age of 16 years). Among these 45 children, 31 children were male (68.9&#x0025;) and 14 were female (31.1&#x0025;); 44 children belonged to the Han race (97.8&#x0025;) and 1 child belonged to the Miao race (2.2&#x0025;). Majority of these children were from Yanjin county, while 1 child was from a neighboring county (Shuifu).</p>
</sec>
<sec id="s3b"><label>3.2.</label><title>Clinical manifestations and laboratory features</title>
<p>All of these cases were clinically diagnosed. The clinical classification is shown in <xref ref-type="table" rid="T1">Table&#x00A0;1</xref>. Among these 45 cases, 25 were of the complex type, 14 were of the thoracopulmonary type, and 6 were of the extrapulmonary type. The clinical symptoms of different clinical types are shown in <xref ref-type="sec" rid="s10">Supplementary Material S1</xref>. Clinical symptoms were closely related to the invaded systems. The most common symptoms were fever, cough, chest pain, and subcutaneous nodules.</p>
<table-wrap id="T1" position="float"><label>Table 1</label>
<caption><p>Characteristic of demographic factors and clinical classification.</p></caption>
<table frame="hsides" rules="groups">
<colgroup>
<col align="left"/>
<col align="left"/>
<col align="center"/>
</colgroup>
<thead>
<tr>
<th valign="top" align="center" colspan="2">Variables</th>
<th valign="top" align="center"><italic>n</italic> (&#x0025;)</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top">Gender</td>
<td valign="top">Male</td>
<td valign="top" align="center">31 (68.89)</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top">Female</td>
<td valign="top" align="center">14 (31.11)</td>
</tr>
<tr>
<td valign="top">Race</td>
<td valign="top">Han</td>
<td valign="top" align="center">44 (97.78)</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top">Miao</td>
<td valign="top" align="center">1 (2.22)</td>
</tr>
<tr>
<td valign="top">Clinical type</td>
<td valign="top"><bold>Thoracopulmonary type</bold></td>
<td valign="top" align="center">14 (31.11)</td>
</tr>
<tr>
<td valign="top" align="left" colspan="3">Simple extrapulmonary type</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top">Abdominal</td>
<td valign="top" align="center">1 (2.22)</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top">Cerebral</td>
<td valign="top" align="center">1 (2.22)</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top">Subcutaneous mass</td>
<td valign="top" align="center">4 (8.89)</td>
</tr>
<tr>
<td valign="top" align="left" colspan="3">Complex type (thoracopulmonary type&#x2009;&#x002B;&#x2009;extrapulmonary type)</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top">Thoracopulmonary&#x2009;&#x002B;&#x2009;abdominal</td>
<td valign="top" align="center">3 (6.67)</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top">Thoracopulmonary&#x2009;&#x002B;&#x2009;cerebral</td>
<td valign="top" align="center">3 (6.67)</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top">Thoracopulmonary&#x2009;&#x002B;&#x2009;pericardium&#x2009;&#x002B;&#x2009;subcutaneous mass</td>
<td valign="top" align="center">8 (17.78)</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top">Thoracopulmonary&#x2009;&#x002B;&#x2009;pericardium</td>
<td valign="top" align="center">3 (6.67)</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top">Thoracopulmonary&#x2009;&#x002B;&#x2009;pericardium&#x2009;&#x002B;&#x2009;abdominal&#x2009;&#x002B;&#x2009;subcutaneous mass</td>
<td valign="top" align="center">3 (6.67)</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top">Thoracopulmonary&#x2009;&#x002B;&#x2009;pericardium&#x2009;&#x002B;&#x2009;abdominal</td>
<td valign="top" align="center">3 (6.67)</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top">Thoracopulmonary&#x2009;&#x002B;&#x2009;subcutaneous mass&#x2009;&#x002B;&#x2009;abdominal</td>
<td valign="top" align="center">1 (2.22)</td>
</tr>
<tr>
<td valign="top" colspan="3">Complex type (extrapulmonary type&#x2009;&#x002B;&#x2009;extrapulmonary type)</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top">Subcutaneous mass&#x2009;&#x002B;&#x2009;pericardium</td>
<td valign="top" align="center">1 (2.22)</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>For all children, results of routine blood tests and ESR were performed at the time of their first visit to the hospital (<xref ref-type="sec" rid="s10">Supplementary Material S2</xref>). The median peripheral white blood cell count in venous blood samples was 11.9&#x002A;10<sup>9</sup>L, and the percentage of eosinophils was elevated in all but one child. ESR was higher than normal in all children. In all children, <italic>Paragonimus</italic> antibody test by the enzyme-linked immunosorbent assay (ELISA) was positive.</p>
<p>On pulmonary CT, the most common findings were pleural effusion (68.9&#x0025;) and alveolar exudation (64.4&#x0025;) (<xref ref-type="sec" rid="s10">Supplementary Material S3</xref>, <xref ref-type="fig" rid="F1">Figure&#x00A0;1</xref>). Brain edema, nodules, and cerebral hemorrhage were found in children with cerebral paragonimiasis (<xref ref-type="sec" rid="s10">Supplementary Material S3</xref>, <xref ref-type="fig" rid="F2">Figure&#x00A0;2</xref>). Pleural effusion was one of the most important findings of ultrasonography. In addition, ultrasound examination also showed abdominal effusion, pericardial effusion, and subcutaneous nodules.</p>
<fig id="F2" position="float"><label>Figure 2</label>
<caption><p>A 5-year-old girl visited our hospital due to limb movement disability. Brain MRI showed the lesion and its surrounding edema (<bold>A, B</bold>), and tunnel-like transitional signs (<bold>C</bold>).</p></caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="fped-11-1143262-g002.tif"/>
</fig>
</sec>
<sec id="s3c"><label>3.3.</label><title>Risk factors</title>
<p>These 45 children had multiple histories of drinking untreated water (<italic>n</italic>&#x2009;&#x003D;&#x2009;16, 35.56&#x0025;), consuming semi-raw/raw freshwater crab meat (<italic>n</italic>&#x2009;&#x003D;&#x2009;25, 55.56&#x0025;), or consuming semi-raw/raw meat (<italic>n</italic>&#x2009;&#x003D;&#x2009;10, 22.22&#x0025;).</p>
</sec>
<sec id="s3d"><label>3.4.</label><title>The experience of misdiagnosis</title>
<p>Before the diagnosis of paragonimiasis, 6 cases had been misdiagnosed (<xref ref-type="table" rid="T2">Table&#x00A0;2</xref>). Three patients presented with &#x201C;fever, cough, and pleural effusion&#x201D;, and were initially diagnosed as having pulmonary tuberculosis. A 5-year-old girl presented with &#x201C;walking instability and vomiting&#x201D;, and she was initially diagnosed with viral encephalitis. Two cases were misdiagnosed as tumors due to &#x201C;fever, local mass, and multiple serous effusions&#x201D;. The anti-tuberculosis treatment and anti-infective therapy were not effective, and the diagnosis was confirmed after detailed diet investigation and antibody detection of <italic>Paragonimus</italic>.</p>
<table-wrap id="T2" position="float"><label>Table 2</label>
<caption><p>Misdiagnosed patient information list.</p></caption>
<table frame="hsides" rules="groups">
<colgroup>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left"/>
</colgroup>
<thead>
<tr>
<th valign="top" align="left">No</th>
<th valign="top" align="center">Age (months)</th>
<th valign="top" align="center">Clinical presentation</th>
<th valign="top" align="center">Initial diagnosis</th>
<th valign="top" align="center">Final diagnosis</th>
<th valign="top" align="center">Time interval<xref ref-type="table-fn" rid="table-fn1">&#x002A;</xref></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">1</td>
<td valign="top" align="left">45</td>
<td valign="top" align="left">Fever, cough, and chest pain</td>
<td valign="top" align="left">Tuberculosis</td>
<td valign="top" align="left">Thoracopulmonary type</td>
<td valign="top" align="left">14 days</td>
</tr>
<tr>
<td valign="top" align="left">2</td>
<td valign="top" align="left">32</td>
<td valign="top" align="left">Fever, cough, and chest pain</td>
<td valign="top" align="left">Tuberculosis</td>
<td valign="top" align="left">Thoracopulmonary type</td>
<td valign="top" align="left">14 days</td>
</tr>
<tr>
<td valign="top" align="left">3</td>
<td valign="top" align="left">106</td>
<td valign="top" align="left">Fever, cough, and increased respiratory rate</td>
<td valign="top" align="left">Tuberculosis</td>
<td valign="top" align="left">Thoracopulmonary&#x2009;&#x002B;&#x2009;pericardium</td>
<td valign="top" align="left">14 days</td>
</tr>
<tr>
<td valign="top" align="left">4</td>
<td valign="top" align="left">96</td>
<td valign="top" align="left">Fever and increased respiratory rate</td>
<td valign="top" align="left">Tumor</td>
<td valign="top" align="left">Thoracopulmonary&#x2009;&#x002B;&#x2009;pericardium&#x2009;&#x002B;&#x2009;abdominal type</td>
<td valign="top" align="left">10 days</td>
</tr>
<tr>
<td valign="top" align="left">5</td>
<td valign="top" align="left">98</td>
<td valign="top" align="left">Fever and increased respiratory rate</td>
<td valign="top" align="left">Tumor</td>
<td valign="top" align="left">Thoracopulmonary&#x2009;&#x002B;&#x2009;pericardium&#x2009;&#x002B;&#x2009;abdominal type</td>
<td valign="top" align="left">10 days</td>
</tr>
<tr>
<td valign="top" align="left">6</td>
<td valign="top" align="left">60</td>
<td valign="top" align="left">Dysphoria</td>
<td valign="top" align="left">Viral encephalitis</td>
<td valign="top" align="left">Cerebral type</td>
<td valign="top" align="left">28 days</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="table-fn1"><label>&#x002A;</label><p>Time interval between the initial and final diagnosis.</p></fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s3e"><label>3.5.</label><title>Treatment and follow-up outcomes</title>
<p>Praziquantel (Shenyang Hongqi Pharmaceutical Co. LTD) was the first drug of choice. It was given orally for three days at a dose of 75&#x2005;mg/kg/day, three times a day, and then it was stopped for four days. The longest course of treatment was 12 weeks in a girl with cerebral paragonimiasis. For children with cerebral paragonimiasis, sedation, mannitol, furosemide and other intracranial pressure-lowering treatments were also given. In addition, adverse reactions to praziquantel, such as anaphylaxis, liver damage, and electrocardiographic abnormalities, were monitored. There was no adverse reaction to praziquantel during treatment.</p>
<p>In 43 cases, the original symptoms were markedly improved and serosal effusion disappeared. Eosinophils and ESR levels returned to normal within three months. The percentage of eosinophils returned to normal. CT or MRI showed narrowing and calcification of the lesion. Most children had a good prognosis, but one child with cerebral paragonimiasis experienced sequelae-limb motor disability. During the follow-up, two children, who were brothers, experienced a re-infection after symptom improvement due to consumption of raw meat again. They were first diagnosed with the thoracopulmonary type; and after treatment, cough symptoms disappeared and chest CT lesions calcified. After about five months, these two patients developed cough and subcutaneous nodules, and the antibody tests of paragonimiasis again turned positive; then, they were diagnosed as having the complex type. These two patients ate raw meat again.</p>
</sec>
</sec>
<sec id="s4" sec-type="discussion"><label>4.</label><title>Discussion</title>
<p>Despite significant improvement in economic and living conditions, paragonimiasis is still one of the diseases that affect the health of children, especially cerebral paragonimiasis. In this study, we retrospectively analyzed the clinical characteristics of 45 children with paragonimiasis in order to improve the recognition of this disease and reduce misdiagnosis.</p>
<p>The clinical manifestations of paragonimiasis in children are diverse and involve many systems, which is closely related to the life history of paragonimiasis. The 45 cases of paragonimiasis included in our study showed 4 clinical subtypes, and many of them were complex and involved multiple systems. The main clinical manifestations included fever, cough, pleural effusion, abdominal effusion, and subcutaneous nodules, which were consistent with previous studies (<xref ref-type="bibr" rid="B7">7</xref>). The results of laboratory and imaging examinations were basically consistent with the clinical symptoms.</p>
<p>Being a foodborne parasitic disease, risk factor is very important for establishing the diagnosis of paragonimiasis. The main ways of human infection with <italic>Paragonimus</italic> are drinking untreated water, consuming raw or semi-raw crayfish and freshwater crab, and consuming raw or semi-raw meat. All children included in this survey had a clear habit of drinking untreated water, eating raw crabs or crayfish, or eating uncooked meat, which is consistent with other studies (<xref ref-type="bibr" rid="B7">7</xref>&#x2013;<xref ref-type="bibr" rid="B9">9</xref>). It is not easy for children to accurately recall their dietary history, and this can also lead to misdiagnosis or delayed diagnosis. We recommend careful and repeated questioning of the primary caregiver (sometimes not their parents). During follow-up, two boys (brothers) experienced re-infection because they did not change their habit of eating raw meat. Thus, changing inappropriate eating habits is a simple and effective way to prevent paragonimiasis.</p>
<p>Etiological diagnosis is the gold standard for the diagnosis of paragonimiasis. In this study, due to technical limitations, we only conducted ELISA. In this study, all children were positive for the <italic>Paragonimus</italic> antibody. In addition to ELISA detection of antibodies, other methods, such as detection of eggs in sputum or feces, and detection of worms or eggs in subcutaneous nodules, other tissues, or body fluids, are also used for etiological determination.</p>
<p>The diversity and lack of specificity of clinical symptoms, signs, and laboratory tests can easily lead to misdiagnosis. As shown in previous studies, paragonimiasis can be easily misdiagnosed as tuberculosis or cancer (<xref ref-type="bibr" rid="B10">10</xref>, <xref ref-type="bibr" rid="B11">11</xref>); 6 cases had been misdiagnosed as tuberculosis, tumor, and viral encephalitis in our study. The radiographic findings, which presented in our results, are also found in other diseases, such as pneumonia, lung neoplasms, tuberculosis, central nervous system neoplasms, vascular diseases, and inflammatory disorders (<xref ref-type="bibr" rid="B10">10</xref>, <xref ref-type="bibr" rid="B12">12</xref>, <xref ref-type="bibr" rid="B13">13</xref>). In addition to paragonimiasis, a significant increase in the percentage of eosinophils is also seen in many diseases, such as allergic diseases, other parasitic infections, eosinophilic gastritis, hypereosinophilic syndrome, and mycotic infection (<xref ref-type="bibr" rid="B10">10</xref>).</p>
<p>The diagnosis of paragonimiasis requires a combination of symptoms, signs, laboratory tests, risk factor, and other factors. In areas with high incidence of pneumofluke disease, the possibility of paragonimiasis should be considered in patients with multi-system symptoms. It is recommended that patients should be carefully enquired about their dietary habits, and etiological detection of <italic>Paragonimus</italic> should be conducted as soon as possible. If necessary, a tissue biopsy can also be used for establishing the diagnosis (<xref ref-type="bibr" rid="B14">14</xref>). CT or MRI may reveal migratory symptoms or the tunnel sign, which are related to the migration of <italic>Paragonimus</italic> larvae, and these findings may be useful to establish the diagnosis (<xref ref-type="bibr" rid="B13">13</xref>, <xref ref-type="bibr" rid="B14">14</xref>).</p>
<p>All children were treated with praziquantel and their symptoms improved after treatment. For cerebral paragonimiasis, surgical intervention is necessary if signs of cerebral herniation occur (<xref ref-type="bibr" rid="B14">14</xref>). In our study, four children with cerebral paragonimiasis were treated with praziquantel for up to 12 weeks. After treatment, headache, vomiting, and other symptoms were relieved, but a 5-year-old girl experienced sequelae (limb motor disability) due to persistence of cerebral tissue injury. In addition, patients with cerebral paragonimiasis may experience other sequelae, such as speech disorders and seizures (<xref ref-type="bibr" rid="B3">3</xref>, <xref ref-type="bibr" rid="B8">8</xref>). Cerebral paragonimiasis is one of the most serious types of paragonimiasis, and it can cause headache, vomiting, movement disorders, seizures, and even death due to intracranial hypertension (<xref ref-type="bibr" rid="B3">3</xref>, <xref ref-type="bibr" rid="B15">15</xref>, <xref ref-type="bibr" rid="B16">16</xref>). All four children had symptoms, such as headache and intracranial hypertension, which were consistent with a previous study (<xref ref-type="bibr" rid="B14">14</xref>). The main pathogenic mechanism of cerebral paragonimiasis is direct and indirect damage to the brain tissue. <italic>Paragonimu</italic>s larvae migrate to the brain tissue, directly destroying the local brain tissue. They can damage different parts of cerebral tissue, and the clinical symptoms also vary. Indirect injury is mainly caused by local brain edema, followed by intracranial hypertension. At this point, patients may present with symptoms of intracranial hypertension, such as headache, vomiting, papilledema, and hypertension (<xref ref-type="bibr" rid="B14">14</xref>).</p>
<p>However, this study has some limitations that should be acknowledged. It was a retrospective study, and a small number of children were included in the study.</p>
</sec>
<sec id="s5" sec-type="conclusions"><label>5.</label><title>Conclusion</title>
<p>An analysis of the clinical, laboratory, and imaging features of children diagnosed with paragonimiasis is helpful to improve the understanding and diagnosis of paragonimiasis. In children, the clinical manifestations of paragonimiasis are diverse and lack specificity, which can easily lead to misdiagnosis. The characteristic tunnel sign on CT or MRI is helpful for making the diagnosis. Children living in areas with high incidence of paragonimiasis and who have fever, cough, local nodules, and multiple serous effusions should be carefully enquired about their dietary habits. Praziquantel is the first drug of choice for the treatment of paragonimiasis. Most patients recover well after treatment, but severe cases may experience sequelae. People living in areas with high incidence of paragonimiasis should be encouraged to change their dietary patterns to prevent paragonimiasis. Avoiding drinking untreated water and eating cold and raw food is a simple but important measure to prevent paragonimiasis.</p>
</sec>
</body>
<back>
<sec id="s6" sec-type="data-availability"><title>Data availability statement</title>
<p>The original contributions presented in the study are included in the article/<xref ref-type="sec" rid="s10"><bold>Supplementary Material</bold></xref>, further inquiries can be directed to the corresponding author/s.</p>
</sec>
<sec id="s7"><title>Ethics statement</title>
<p>The studies involving human participants were reviewed and approved by Xinhua Hospital affiliated to Shanghai Jiao Tong University School of Medicine. Written informed consent from the participants&#x2019; legal guardian/next of kin was not required to participate in this study in accordance with the national legislation and the institutional requirements.</p>
</sec>
<sec id="s8"><title>Author contributions</title>
<p>JY: contributed to program design, data analysis, writing manuscript; LG: contributed to data collection, case admission and analysis; PC, HZ, WC and MQ: contributed to case admission, data collection; CL: contributed to program design, proposal methodology, quality control, review and editing the manuscript. All authors contributed to the article and approved the submitted version.</p>
</sec>
<ack><title>Acknowledgments</title>
<p>We sincerely thank the children and their parents who participated in this study.</p>
</ack>
<sec id="s9" sec-type="COI-statement"><title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec id="s11" sec-type="disclaimer"><title>Publisher&#x0027;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
<sec id="s10" sec-type="supplementary-material"><title>Supplementary material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fped.2023.1143262/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fped.2023.1143262/full&#x0023;supplementary-material</ext-link>.</p>
<supplementary-material id="SD1" content-type="local-data">
<media mimetype="application" mime-subtype="vnd.openxmlformats-officedocument.wordprocessingml.document" xlink:href="Table1.docx"/>
</supplementary-material>
</sec>
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