<?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.161989.1</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: Case report: A perforated right ovarian teratoma misdiagnosed as appendicular abscess</article-title>
                <fn-group content-type="pub-status">
                    <fn>
                        <p>[version 1; peer review: 1 approved]</p>
                    </fn>
                </fn-group>
            </title-group>
            <contrib-group>
                <contrib contrib-type="author" corresp="yes">
                    <name>
                        <surname>HIDOURI</surname>
                        <given-names>Saida</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Conceptualization</role>
                    <role content-type="http://credit.niso.org/">Supervision</role>
                    <role content-type="http://credit.niso.org/">Validation</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/0000-0003-3220-8028</uri>
                    <xref ref-type="corresp" rid="c1">a</xref>
                    <xref ref-type="aff" rid="a1">1</xref>
                    <xref ref-type="aff" rid="a2">2</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>Ben AMMAR</surname>
                        <given-names>Sabrine</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Conceptualization</role>
                    <role content-type="http://credit.niso.org/">Methodology</role>
                    <role content-type="http://credit.niso.org/">Writing &#x2013; Original Draft Preparation</role>
                    <xref ref-type="aff" rid="a1">1</xref>
                    <xref ref-type="aff" rid="a2">2</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>ELMANSOURY</surname>
                        <given-names>Yosra</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Methodology</role>
                    <xref ref-type="aff" rid="a3">3</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>AZIZA</surname>
                        <given-names>Bochra</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Methodology</role>
                    <xref ref-type="aff" rid="a3">3</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>SAHRAOUI</surname>
                        <given-names>Ghada</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Data Curation</role>
                    <role content-type="http://credit.niso.org/">Visualization</role>
                    <xref ref-type="aff" rid="a4">4</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>SAHLI</surname>
                        <given-names>Sondos</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Validation</role>
                    <role content-type="http://credit.niso.org/">Visualization</role>
                    <xref ref-type="aff" rid="a3">3</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>HABACHI</surname>
                        <given-names>Ghada</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Methodology</role>
                    <xref ref-type="aff" rid="a3">3</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>JOUINI</surname>
                        <given-names>Riadh</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Validation</role>
                    <role content-type="http://credit.niso.org/">Visualization</role>
                    <xref ref-type="aff" rid="a3">3</xref>
                </contrib>
                <aff id="a1">
                    <label>1</label>Research Laboratory LR12SP13, University of Monastir Faculty of Medicine of Monastir, Monastir, 5000, Tunisia</aff>
                <aff id="a2">
                    <label>2</label>Department of Paediatric Surgery, Hospital of Zaghouan, Zaghouan, 1100, Tunisia</aff>
                <aff id="a3">
                    <label>3</label>Department of Paediatric Surgery &#x201c;A&#x201d;, Children&#x2019;s Hospital of Tunis, Tunis, 1029, Tunisia</aff>
                <aff id="a4">
                    <label>4</label>Department of Pathology, Salah Azaiez Institute, Tunis, 1029, Tunisia</aff>
            </contrib-group>
            <author-notes>
                <corresp id="c1">
                    <label>a</label>
                    <email xlink:href="mailto:saida.hidouri2020@gmail.com">saida.hidouri2020@gmail.com</email>
                </corresp>
                <fn fn-type="conflict">
                    <p>No competing interests were disclosed.</p>
                </fn>
            </author-notes>
            <pub-date pub-type="epub">
                <day>6</day>
                <month>3</month>
                <year>2025</year>
            </pub-date>
            <pub-date pub-type="collection">
                <year>2025</year>
            </pub-date>
            <volume>14</volume>
            <elocation-id>271</elocation-id>
            <history>
                <date date-type="accepted">
                    <day>22</day>
                    <month>2</month>
                    <year>2025</year>
                </date>
            </history>
            <permissions>
                <copyright-statement>Copyright: &#x00a9; 2025 HIDOURI S et al.</copyright-statement>
                <copyright-year>2025</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/14-271/pdf"/>
            <abstract>
                <sec>
                    <title>Introduction</title>
                    <p>Perforation of mature ovarian teratomas is rare. This revelation may be misleading. We report a unique case of a ruptured teratoma mimicking an appendicular abscess, emphasizing the value of sharing such an experience to learn from our mistakes as well as the importance of a conservative approach in the treatment of these tumors in children.</p>
                </sec>
                <sec>
                    <title>Case description</title>
                    <p>A 12-year-old-girl presented to the emergency room with a 3-days history of worsening abdominal pain. She reported a fever associated with vomiting and diarrhea. On physical examination, the patient was feverish and displayed generalized tenderness, especially in the right iliac fossa where there was a palpable mass. white blood cell count and C-reactive protein levels were significantly elevated. Abdominal ultrasonography confirmed appendicular abscess. Intraoperatively, a perforated right ovarian teratoma was found, and ovarian sparing surgery was performed. No postoperative complications were noted, and histology confirmed the diagnosis of a mature teratoma.</p>
                </sec>
                <sec>
                    <title>Conclusion</title>
                    <p>The differential diagnosis of acute abdominal pain in girls is broad and includes gynecological disorders. Ovarian teratomas can progress silently. In this case, the diagnosis can be made intraoperatively when a complication has occurred. Surgeons and radiologists are not always able to establish a positive diagnosis when there are no obvious clinicoradiological features. Even when the diagnosis is made intraoperatively, treatment must be appropriate and conservative surgery remains a therapeutic option.</p>
                </sec>
            </abstract>
            <kwd-group kwd-group-type="author">
                <kwd>Abdominal pain</kwd>
                <kwd>Appendicitis</kwd>
                <kwd>Child</kwd>
                <kwd>Complication</kwd>
                <kwd>Diagnosis</kwd>
                <kwd>Differential</kwd>
                <kwd>Ovarian Neoplasms</kwd>
                <kwd>Teratoma</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 id="sec4" sec-type="intro">
            <title>Introduction</title>
            <p>Mature teratomas are a common type of ovarian tumor in children
                <sup>
                    <xref ref-type="bibr" rid="ref1">1</xref>
                </sup> and are often diagnosed incidentally on imaging, which demonstrates specific findings.
                <sup>
                    <xref ref-type="bibr" rid="ref2">2</xref>
                </sup> Ovarian teratomas are characterized by slow and subtle growth patterns, frequently resulting in delayed diagnosis.
                <sup>
                    <xref ref-type="bibr" rid="ref3">3</xref>
                </sup> Symptomatic cases may involve complicated or large masses.
                <sup>
                    <xref ref-type="bibr" rid="ref3">3</xref>
                </sup> Some forms of presentation, particularly in prepubescent girls and in the case of large lesions, make diagnosis more difficult. Computed tomography and magnetic resonance imaging (MRI) scans can be beneficial.
                <sup>
                    <xref ref-type="bibr" rid="ref3">3</xref>
                </sup>
            </p>
            <p>Teratoma complications may arise, especially in cases of large tumors.
                <sup>
                    <xref ref-type="bibr" rid="ref2">2</xref>
                </sup> Spontaneous rupture occurs in only 3.8% of the cases.
                <sup>
                    <xref ref-type="bibr" rid="ref2">2</xref>
                </sup> This low rate is attributed to the presence of a thick protective capsule.
                <sup>
                    <xref ref-type="bibr" rid="ref2">2</xref>
                </sup> Rupture may occur in the peritoneal cavity or a hollow organ in the surrounding area. Potential predisposing factors for such accidents include ischemia and necrosis of the mass wall, infection, trauma, and malignant transformation.
                <sup>
                    <xref ref-type="bibr" rid="ref4">4</xref>
                </sup> It can present with an acute abdomen or chronic granulomatous peritonitis.
                <sup>
                    <xref ref-type="bibr" rid="ref5">5</xref>
                </sup>
            </p>
            <p>We report a case of a ruptured mature right ovarian teratoma causing an acute abdomen that was misdiagnosed as appendicular abscess. Here, we discuss the clinical and radiologic non-specificity of these tumors in the context of complications and aspects of confusion to help surgeons anticipate such an intraoperative surprise. We also support the possibility of conservative treatment, even in the presence of such complications.</p>
        </sec>
        <sec id="sec5">
            <title>Case report</title>
            <sec id="sec6">
                <title>Patient information</title>
                <p>A 12-year-old previously healthy girl presented to our emergency room with a 3-day history of worsening abdominal pain predominantly located in the right iliac fossa. There was no family history of the evaluation. Her menarche occurred at 11 years of age, her menstrual cycles were regular, and her last menstrual period was one week ago.</p>
            </sec>
            <sec id="sec7">
                <title>Initial clinical findings</title>
                <p>The patient described acute onset of abdominal pain with no concept of trauma, accompanied by fever, vomiting, and diarrhea.</p>
            </sec>
            <sec id="sec8">
                <title>Physical examination</title>
                <p>On physical examination, normal hemodynamic parameters were maintained, the patient was febrile at 38.8&#x00b0;C and had generalized tenderness, especially over the right iliac fossa. There was a palpable, firm, painful mass in the right iliac fossa that extended for at least 130 mm, with no signs of inflammation at this site. Examination of the genitals revealed a pubescent girl with patent hymen.</p>
            </sec>
            <sec id="sec9">
                <title>Diagnostic assessments</title>
                <p>An emergency biology test showed that the white blood cell count (WBC) and C-reactive protein (CRP) level were significantly elevated at 16800/mm
                    <sup>3</sup> (4000&#x2013;10000/mm
                    <sup>3</sup>) and 140 mg/L (normal value &lt;5 mg/L), respectively.</p>
                <p>Given this clinical context, palpable mass, and biological anomalies, we suspected acute appendicitis complicated by an abscess. Immediate abdominal ultrasound performed by a non-experimented radiologist showed poorly limited collection with a heterogeneous echogenic content seat of echogenic spots related to extra-digestive air bubbles (
                    <xref ref-type="fig" rid="f1">
Figure 1</xref>). The collection was 123 &#x00d7; 154 mm in size, occupying the right lower hemiabdomen. Intraperitoneal fat infiltration and a finely echogenic, moderately abundant effusion were also observed. Given the size of the collection, identification of the appendix or the right ovary was not obvious.</p>
                <fig fig-type="figure" id="f1" orientation="portrait" position="float">
                    <label>
Figure 1. </label>
                    <caption>
                        <title>A sonogram showing a large heterogeneous collection (the arrow) in the right lower abdomen.</title>
                    </caption>
                    <graphic id="gr1" orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/178107/1627417a-3556-4550-81c2-00d5ce1e25c1_figure1.gif"/>
                </fig>
            </sec>
            <sec id="sec10">
                <title>Therapeutic intervention</title>
                <p>The patient was perfused, monitored, and administered parenteral antibiotic therapy. The patient was then operated on via laparotomy using a McBurney incision. Intraoperatively, effusion was widespread and consisted of serous fluid, sebum, and calcium debris. The patient also had a perforated right ovarian teratoma. The mass was large, measuring 150 &#x00d7; 120 mm, with a unique small capsule perforation (
                    <xref ref-type="fig" rid="f2">
Figure 2</xref>). The tumor displaced the surrounding intact ovarian parenchyma, and there were no signs of adnexal torsion. The appendix appeared normal and hidden by the mass. The contralateral ovary was completely normal, and there were no metastases or peritoneal granulations.</p>
                <fig fig-type="figure" id="f2" orientation="portrait" position="float">
                    <label>
Figure 2. </label>
                    <caption>
                        <title>Ovarian teratoma (A) with a small focus rupture (the arrow) surrounding by the normal ovary (B).</title>
                    </caption>
                    <graphic id="gr2" orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/178107/1627417a-3556-4550-81c2-00d5ce1e25c1_figure2.gif"/>
                </fig>
                <p>Extemporaneous histological examinations were unavailable; however, there was no evidence of malignancy. Based on the patient&#x2019;s age and aforementioned operative findings, we opted for conservative treatment. The mass was removed (
                    <xref ref-type="fig" rid="f3">
Figure 3</xref>), leaving the surrounding normal ovarian tissue in place, and peritoneal cleaning was performed.</p>
                <fig fig-type="figure" id="f3" orientation="portrait" position="float">
                    <label>
Figure 3. </label>
                    <caption>
                        <title>The entire ovarian mass resected with effusion of small nodules (the arrow).</title>
                    </caption>
                    <graphic id="gr3" orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/178107/1627417a-3556-4550-81c2-00d5ce1e25c1_figure3.gif"/>
                </fig>
            </sec>
            <sec id="sec11">
                <title>Follow-up and outcomes</title>
                <p>The postoperative course was uneventful, and the patient was discharged three days later. Tumor markers (AFP, HCG, CA19-9, CA-125, LDH, and Inhibin) tested immediately after surgery were negative. Histology (
                    <xref ref-type="fig" rid="f4">
Figure 4</xref>) and peritoneal lavage samples confirmed the benign nature of teratoma containing a mixture of mature benign tissues (e.g., cartilage, sebaceous glands, pancreatic tissue), as well as the complete removal of the mass. Clinical and ultrasound checkups were free of any homo-or contralateral recurrence, with a follow-up period of twenty-three months.</p>
                <fig fig-type="figure" id="f4" orientation="portrait" position="float">
                    <label>
Figure 4. </label>
                    <caption>
                        <title>The histological examination revealing mature cartilage lobules (A) and a cutaneous tissue covered by a regular epidermis and supported by a dermis with pilo-sebaceous appendages (B).</title>
                    </caption>
                    <graphic id="gr4" orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/178107/1627417a-3556-4550-81c2-00d5ce1e25c1_figure4.gif"/>
                </fig>
            </sec>
        </sec>
        <sec id="sec12" sec-type="discussion">
            <title>Discussion</title>
            <p>Rupture of an ovarian teratoma is not a common cause of acute abdomen in females. Herein, we discuss the contribution of thorough clinical and radiological investigations to the assessment of this rare condition. The distinction between acute appendicitis and teratoma ovarian rupture is the focus of this case report. Our second concern was to advocate for conservative ovarian surgery, even when faced with this complication.</p>
            <p>One of the most common pediatric surgical emergencies is acute appendicitis, including complicated cases.
                <sup>
                    <xref ref-type="bibr" rid="ref6">6</xref>&#x2013;
                    <xref ref-type="bibr" rid="ref9">9</xref>
                </sup> In prepubertal girls, gynecologic emergencies are the most important differential diagnosis.
                <sup>
                    <xref ref-type="bibr" rid="ref7">7</xref>
                </sup> Complicated right ovarian teratoma may be an imitator of acute appendicitis, as in the case of our patient and others reported in the literature, due to the nearness of the appendix and the ovary.
                <sup>
                    <xref ref-type="bibr" rid="ref4">4</xref>,
                    <xref ref-type="bibr" rid="ref7">7</xref>
                </sup> Several factors may contribute to this clinical-radiological confusion. From a clinical point of view, a collection in the right iliac fossa in a child, even in a girl, is initially suggestive of appendicular abscess.
                <sup>
                    <xref ref-type="bibr" rid="ref10">10</xref>
                </sup> However, apyrexia, the patient&#x2019;s general and hemodynamic stability, the absence of vomiting, and local signs of inflammation contradict this diagnosis.
                <sup>
                    <xref ref-type="bibr" rid="ref10">10</xref>
                </sup>
            </p>
            <p>Pain in the right iliac fossa is the first sign of appendicitis. This pain is usually tolerated at onset and is continuous and progressively worse,
                <sup>
                    <xref ref-type="bibr" rid="ref11">11</xref>
                </sup> as described by our patient. Nevertheless, it is crucial to investigate the concept of intermittent and mild chronic abdominal pain characterized by a feeling of abdominal heaviness, generally associated with ovarian mature teratoma.
                <sup>
                    <xref ref-type="bibr" rid="ref12">12</xref>,
                    <xref ref-type="bibr" rid="ref13">13</xref>
                </sup> This pain can be attributed to the compressive effect of the large mass.
                <sup>
                    <xref ref-type="bibr" rid="ref7">7</xref>
                </sup> Although the acute, sudden appearance of abdominal pain in a girl should draw attention to the possibility of ovarian torsion,
                <sup>
                    <xref ref-type="bibr" rid="ref12">12</xref>
                </sup> a more frequent condition, any modification in the characteristics of the sub-chronic right-sided abdominal pain, which becomes intense and accompanied by vomiting or nausea, is suggestive of rupture of an ovarian teratoma.
                <sup>
                    <xref ref-type="bibr" rid="ref14">14</xref>
                </sup> These circumstances may have a confusing clinical presentation, particularly when mimicking an acute abdominal situation. In such cases, imaging is either inconclusive or not allowed by the state of emergency. Fever and transit disorders may also occur in these complicated teratomas owing to inflammatory and peritoneal irritation processes.
                <sup>
                    <xref ref-type="bibr" rid="ref7">7</xref>
                </sup>
            </p>
            <p>On imaging, abdominal plain radiography can have an informative role as it may show calcifications and deviation of the digestive structures in relation to the mass.
                <sup>
                    <xref ref-type="bibr" rid="ref6">6</xref>
                </sup> However, this type of imaging is not routinely performed for acute right iliac fossa pain. Abdominal ultrasound is the first imaging modality requested for girls with acute febrile abdominal pain, given its common gynecological etiology.
                <sup>
                    <xref ref-type="bibr" rid="ref9">9</xref>
                </sup> For acute teratoma rupture, the detection of discontinuity in the tumor wall is a diagnostic key
                <sup>
                    <xref ref-type="bibr" rid="ref5">5</xref>,
                    <xref ref-type="bibr" rid="ref15">15</xref>
                </sup>; however, this was not obvious in our case. Another radiologic feature that deserves more attention is the non-visibility of the appendix, which may be located outside the right iliac fossa or even obscured by the intestine or a large mass, as in our case. A gynecological cause is still expected in such cases.</p>
            <p>If this condition is allowed, further investigations are required and will be more useful for diagnosis. Computed tomography (CT) is a more sensitive imaging modality, revealing acute ruptured hemoperitoneum with floating fat globules.
                <sup>
                    <xref ref-type="bibr" rid="ref2">2</xref>,
                    <xref ref-type="bibr" rid="ref5">5</xref>,
                    <xref ref-type="bibr" rid="ref15">15</xref>
                </sup> Tumors with only a small focus rupture may cause granulomatous chronic peritonitis, which appears to be tuberculosis or peritoneal carcinomatosis on imaging.
                <sup>
                    <xref ref-type="bibr" rid="ref5">5</xref>,
                    <xref ref-type="bibr" rid="ref14">14</xref>,
                    <xref ref-type="bibr" rid="ref15">15</xref>
                </sup> Pelvic Magnetic Resonance Imaging is used to better characterize the mass and detect fat
                <sup>
                    <xref ref-type="bibr" rid="ref16">16</xref>
                </sup>; however, it is not systematically available and may require general anesthesia in children. Laparoscopy is considered a useful diagnostic tool for cases in which imaging is not accurate. Regardless of the diagnostic tool, when evaluating right iliac fossa pain in females, especially those of prepubertal age, clinicians should consider gynecologic causes to improve diagnosis precision.</p>
            <p>In most cases, mature ovarian tumors are treated conservatively; the surgical approach may be either laparotomy or laparoscopy, and both approaches have comparable complication rates.
                <sup>
                    <xref ref-type="bibr" rid="ref13">13</xref>,
                    <xref ref-type="bibr" rid="ref17">17</xref>
                </sup> Single-incision laparoscopic surgery has also proven to be effective in pelvic tumor surgery
                <sup>
                    <xref ref-type="bibr" rid="ref18">18</xref>
                </sup>; however, the choice of approach depends on the patient and the characteristics of the mass.</p>
            <p>The usefulness of ovarian sparing surgery in the pediatric population has been approved considering the long-term consequences of unilateral oophorectomy and the potential risk of contralateral ovarian tumor development.
                <sup>
                    <xref ref-type="bibr" rid="ref17">17</xref>,
                    <xref ref-type="bibr" rid="ref19">19</xref>
                </sup> If the mass is well limited and can be safely removed from the ovarian parenchyma, conservative treatment is appropriate, even in the case of large ruptured benign tumors.
                <sup>
                    <xref ref-type="bibr" rid="ref17">17</xref>,
                    <xref ref-type="bibr" rid="ref19">19</xref>
                </sup> One review reported that ovarian-sparing surgery is associated with minimal recurrence and repeat surgery rates.
                <sup>
                    <xref ref-type="bibr" rid="ref19">19</xref>
                </sup> Preoperatively, apart from complications, the benign nature of the mass is determined based on symptoms, radiologic features, and tumor markers. However, in the case of an acute presentation, the challenge remains to distinguish between a benign and malignant mass intraoperatively, as was the case with our patient. In these cases, the surgeon's estimation and pathologist's analysis will determine the therapeutic option.</p>
            <sec id="sec13">
                <title>Strengths and limitations</title>
                <p>Our case report may not present a complete review of all possible outcomes, which may limit the ability to draw definitive conclusions. Nevertheless, it provides a detailed example of an unusual presentation of an ovarian teratoma. This may help clinicians to better recognize the diagnostic challenges of these tumors and guide their treatment decisions when encountering similar situations.</p>
            </sec>
        </sec>
        <sec id="sec14" sec-type="conclusion">
            <title>Conclusion</title>
            <p>Numerous incidents are associated with ovarian teratomas, especially when they are large. These circumstances may have a confusing clinical presentation, particularly when mimicking an acute abdominal situation. In such cases, imaging is either inconclusive or not allowed by the state of emergency. In young girls, acute abdominal pain should be given more attention because of the common occurrence of gynecological pathologies. Conservative treatment for benign complicated teratomas should be considered even with an intraoperative diagnosis.</p>
            <sec id="sec15">
                <title>Patient perspective</title>
                <p>The patient&#x2019;s perspective was documented in the form of a video (available if requested). The translated text is as follows: The ailment in question afflicted me three years ago, and I am now fully recovered. I recall experiencing severe right abdominal discomfort accompanied by other symptoms including fever and vomiting. On arrival at the emergency room, the physician suspected acute appendicitis and recommended surgical intervention. I initially experienced trepidation, but as the recommended analgesic treatment took effect, my condition began to improve, thereby providing me with greater reassurance. The patient&#x2019;s condition was satisfactory following the surgical procedure. We did not anticipate the existence of such a sizable cyst. I was fortunate to have been discharged from the hospital in a timely manner so that I could return to my academic duties.</p>
            </sec>
        </sec>
        <sec id="sec16">
            <title>Ethical approval</title>
            <p>Ethical approval was not required.</p>
        </sec>
        <sec id="sec17">
            <title>Consent</title>
            <p>Written informed consent for publication of clinical details and clinical images was obtained from the parents of the patient.</p>
        </sec>
    </body>
    <back>
        <sec id="sec20" sec-type="data-availability">
            <title>Data availability statement</title>
            <p>No data are associated with this article.</p>
        </sec>
        <ref-list>
            <title>References</title>
            <ref id="ref1">
                <label>1</label>
                <mixed-citation publication-type="journal">
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    <sub-article article-type="reviewer-report" id="report397937">
        <front-stub>
            <article-id pub-id-type="doi">10.5256/f1000research.178107.r397937</article-id>
            <title-group>
                <article-title>Reviewer response for version 1</article-title>
            </title-group>
            <contrib-group>
                <contrib contrib-type="author">
                    <name>
                        <surname>Okebalama</surname>
                        <given-names>Victor Chimezie</given-names>
                    </name>
                    <xref ref-type="aff" rid="r397937a1">1</xref>
                    <role>Referee</role>
                    <uri content-type="orcid">https://orcid.org/0000-0002-7956-6773</uri>
                </contrib>
                <aff id="r397937a1">
                    <label>1</label>Babcock University Teaching Hospital, Ilishan-Remo, Ogun State, Nigeria</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>3</day>
                <month>9</month>
                <year>2025</year>
            </pub-date>
            <permissions>
                <copyright-statement>Copyright: &#x00a9; 2025 Okebalama VC</copyright-statement>
                <copyright-year>2025</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="relatedArticleReport397937" related-article-type="peer-reviewed-article" xlink:href="10.12688/f1000research.161989.1"/>
            <custom-meta-group>
                <custom-meta>
                    <meta-name>recommendation</meta-name>
                    <meta-value>approve</meta-value>
                </custom-meta>
            </custom-meta-group>
        </front-stub>
        <body>
            <p>Please clearly state (within the abstract) the initial clinical diagnosis before histology. This should also be done within the case report subheading.&#x00a0;</p>
            <p> </p>
            <p> Was the appendix examined intraoperatively? Clearly state the findings.&#x00a0;</p>
            <p> </p>
            <p> Please clearly annotate&#x00a0;the histology photomicrographs with arrows of different colors for the different components of your histological diagnosis.</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>Pathology, public health, application of technology in healthcare, surgery, obstetrics and gynecology, and medicine.</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>
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