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<article xml:lang="en" article-type="case-report" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<?release-delay 0|0?>
<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">ETM</journal-id>
<journal-title-group>
<journal-title>Experimental and Therapeutic Medicine</journal-title>
</journal-title-group>
<issn pub-type="ppub">1792-0981</issn>
<issn pub-type="epub">1792-1015</issn>
<publisher>
<publisher-name>D.A. Spandidos</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">ETM-26-3-12157</article-id>
<article-id pub-id-type="doi">10.3892/etm.2023.12157</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Case report</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Intraoral approach for the treatment of non‑infiltrating angiolipoma of the floor of the mouth in an elderly patient: A case report with review of the literature</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name><surname>Kang</surname><given-names>Yei-Jin</given-names></name>
<xref rid="af1-ETM-26-3-12157" ref-type="aff">1</xref>
<xref rid="c1-ETM-26-3-12157" ref-type="corresp"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Lee</surname><given-names>Sang-Shin</given-names></name>
<xref rid="af2-ETM-26-3-12157" ref-type="aff">2</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Kim</surname><given-names>Seong-Gon</given-names></name>
<xref rid="af3-ETM-26-3-12157" ref-type="aff">3</xref>
</contrib>
</contrib-group>
<aff id="af1-ETM-26-3-12157"><label>1</label>Department of Oral and Maxillofacial Surgery, Gangneung-Wonju National University Dental Hospital, Gangneung, Gangwon 25457, Republic of Korea</aff>
<aff id="af2-ETM-26-3-12157"><label>2</label>Department of Oral and Maxillofacial Pathology, College of Dentistry, Gangneung-Wonju National University, Gangneung, Gangwon 25457, Republic of Korea</aff>
<aff id="af3-ETM-26-3-12157"><label>3</label>Department of Oral and Maxillofacial Surgery, College of Dentistry, Gangneung-Wonju National University, Gangneung, Gangwon 25457, Republic of Korea</aff>
<author-notes>
<corresp id="c1-ETM-26-3-12157"><italic>Correspondence to:</italic> Dr Yei-Jin Kang, Department of Oral and Maxillofacial Surgery, Gangneung-Wonju National University Dental Hospital, 7 Jukheon, Gangneung, Gangwon 25457, Republic of Korea <email>kyj292@hanmail.net sunchang@snnu.edu.cn </email></corresp>
</author-notes>
<pub-date pub-type="collection">
<month>09</month>
<year>2023</year></pub-date>
<pub-date pub-type="epub">
<day>04</day>
<month>08</month>
<year>2023</year></pub-date>
<volume>26</volume>
<issue>3</issue>
<elocation-id>458</elocation-id>
<history>
<date date-type="received">
<day>25</day>
<month>03</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>10</day>
<month>07</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright: &#x00A9; Kang et al.</copyright-statement>
<copyright-year>2020</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-nc-nd/4.0/">Creative Commons Attribution-NonCommercial-NoDerivs License</ext-link>, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.</license-p></license>
</permissions>
<abstract>
<p>A 75-year-old male patient visited Gangneung-Wonju National University Dental Hospital (Gangneung, South Korea) with a 35-mm fluctuant lesion on the floor of the mouth. It was a dome-shaped exophytic lesion with its top on Wharton&#x0027;s duct orifice area. The encapsulated lesion was excised cautiously and the final diagnosis was non-infiltrating angiolipoma. To the best of our knowledge, this is the first report of an intraoral approach for the treatment of a non-infiltrating angiolipoma on the floor of the mouth in an elderly patient. Differentiating it from a ranula is essential for the surgical approach and, as there is a higher transition to infiltrating angiolipoma, definite treatment should be considered in elderly patients.</p>
</abstract>
<kwd-group>
<kwd>angiolipoma</kwd>
<kwd>elderly</kwd>
<kwd>excision</kwd>
<kwd>ranula</kwd>
<kwd>marsupialisation</kwd>
</kwd-group>
<funding-group>
<funding-statement><bold>Funding:</bold> This study was supported financially by Gangneung-Wonju National University Dental Hospital (Gangneung, Gangwon, Korea).</funding-statement>
</funding-group>
</article-meta>
</front>
<body>
<sec sec-type="intro">
<title>Introduction</title>
<p>Angiolipomas are benign mesenchymal tumours composed of mature lipocytes and vessels and are a subtype of lipomas (<xref rid="b1-ETM-26-3-12157" ref-type="bibr">1</xref>,<xref rid="b2-ETM-26-3-12157" ref-type="bibr">2</xref>). They represent 5-17&#x0025; of lipomas (<xref rid="b2-ETM-26-3-12157" ref-type="bibr">2</xref>) and are infrequent in the oral area (<xref rid="b1-ETM-26-3-12157" ref-type="bibr">1</xref>). According to previous literature, the mean age of affected patients is 37 years (other oral lipomas: Fifties and sixties; cutaneous lipoma: Younger patients) (<xref rid="b3-ETM-26-3-12157" ref-type="bibr">3</xref>,<xref rid="b4-ETM-26-3-12157" ref-type="bibr">4</xref>). Angiolipomas are classified as non-infiltrating and less frequently infiltrating (<xref rid="b5-ETM-26-3-12157 b6-ETM-26-3-12157 b7-ETM-26-3-12157" ref-type="bibr">5-7</xref>). The non-infiltrating lesions are encapsulated and lack evidence of adjacent tissue invasion. The diameter of these lesions is generally #x003C;4 cm and they are more common in adolescents and young adults (<xref rid="b5-ETM-26-3-12157" ref-type="bibr">5</xref>). Infiltrating angiolipomas lack a circumferential capsule and are characterised by adjacent structure invasion and difficulty separating the masses from the surrounding tissues (<xref rid="b8-ETM-26-3-12157" ref-type="bibr">8</xref>). Although benign, inadequate excision may lead to recurrence (<xref rid="b9-ETM-26-3-12157" ref-type="bibr">9</xref>). Infiltrating angiolipomas appear more frequent in elderly patients (<xref rid="b9-ETM-26-3-12157" ref-type="bibr">9</xref>). The present study reported a rare case of a non-infiltrating angiolipoma on the floor of the mouth in an elderly patient. To the best of our knowledge, this is the first report of an intraoral approach for the treatment of non-infiltrating angiolipoma of the floor of the mouth in an elderly patient. This study was approved by the Institutional Review Board (IRB) of Gangneung-Wonju National University Dental Hospital (Gangneung, Korea; no. GWNUDH-IRB2022-A013).</p>
</sec>
<sec sec-type="Case|report">
<title>Case report</title>
<p>A 75-year-old male patient with normal body weight visited Gangneung-Wonju National University Dental Hospital (Gangneung, South Korea) in April 2022 with a 35 mm-sized fluctuant pink lesion on the floor of the mouth. The lesion was dome-shaped and exophytic, with its top on the orifice area of Wharton&#x0027;s duct (<xref rid="f1-ETM-26-3-12157" ref-type="fig">Fig. 1</xref>). The patient was asymptomatic and had noticed the tumour 30 years before the visit, and it had been gradually increasing in size. When the first interviewer asked about pain before meals to rule out salivary gland-related lesions, the patient reported no food intake-related pain. However, the patient had dry mouth symptoms and the lesion elevated the tongue and interfered with speech and swallowing. Physical examination of the lesion revealed soft, mobile, tender and slow-growing masses, and the following differential diagnoses were considered: Ranula, haemangioma, lipoma, leiomyoma and neurilemmoma (<xref rid="b9-ETM-26-3-12157" ref-type="bibr">9</xref>).</p>
<p>Enhanced computed tomography was performed for further evaluation. However, it is impossible to differentiate between ranula and lipoma based on Hounsfield units (ranula, 100; lipoma, 65-120), and due to artefacts from the dental crown, evaluation of soft tissue swelling in the mouth floor was impossible. The peripheral bone tissue exhibited no abnormal signs. Nodal enlargement in the submandibular and submental areas was detected and considered as reactive lymph nodes (<xref rid="f2-ETM-26-3-12157" ref-type="fig">Fig. 2</xref>). Given the features of the tumor, including its slow growth rate and clear margin, our initial assessment indicated a high likelihood of it being a benign mass. Consequently, no pre-operative plan for conducting frozen pathology was established. However, it is important to note that, while the tumor exhibited characteristics of a benign lesion, it is still possible for long-standing benign masses to undergo malignant transformation over time. Recently, the patient had experienced xerostomia and it was not possible to see whether the lesion had a yellowish color due to its deep location. The floor of the mouth contains numerous salivary glands, including the sublingual gland and the Warton&#x0027;s duct is also present. In addition, there was a possibility for dehiscence in the mylohyoid muscle, allowing mucus to drain into the submandibular space, resulting in a condition known as a &#x2018;plunging ranula&#x2019;. The clinical diagnosis before surgery was ranula.</p>
<p>Despite the patient&#x0027;s age, ranula, which is prevalent in children, could not be ruled out, and for this reason, marsupialisation and fibrin glue injection would have been required (<xref rid="b10-ETM-26-3-12157" ref-type="bibr">10</xref>). Under general anaesthesia, an intraoral incision was made in the lesion&#x0027;s periphery as a trapdoor, preserving the Wharton&#x0027;s duct (<xref rid="f3-ETM-26-3-12157" ref-type="fig">Fig. 3</xref>). When a small incision was made at the margin of the exophytic lesion on the floor of the mouth, the soft yellowish tissue extruded slightly. As this yellowish mass resembled adipose tissue, the treatment plan was changed from marsupialisation to surgical excision. The mass was well encapsulated. The encapsulated lesion was excised (<xref rid="f4-ETM-26-3-12157" ref-type="fig">Fig. 4</xref>) and referred for pathological examination with an adjacent tissue (trapdoor) sample.</p>
<p>For pathological evaluation, Harris hematoxylin &#x0026; eosin (regressive) stain was performed according to standard procedures. Prior to staining, samples were fixed using 10&#x0025; neutral buffered formalin for 24 h at room temperature (20&#x02DA;C). The thickness of the sections was 4 &#x00B5;m and staining was performed at room temperature (20&#x02DA;C; 1 and 5 min). An Olympus BX50 muti microscope (Olympus Corp.) was used for analysis. The specimens revealed large fibrous stroma-encapsulated fatty tissue without atypia. Numerous capillaries proliferated into the fatty tissue. The capillaries contained fibrin thrombi (<xref rid="b11-ETM-26-3-12157" ref-type="bibr">11</xref>) and fibrofatty changes (<xref rid="b12-ETM-26-3-12157" ref-type="bibr">12</xref>). The adjacent tissue exhibited loose collagenised fibrous epithelial tissue with capillary proliferation. No infiltration of adipose cells was observed in this specimen and no atypical changes were observed (<xref rid="f5-ETM-26-3-12157" ref-type="fig">Fig. 5</xref>).</p>
<p>The final diagnosis was non-infiltrating angiolipoma. The symptoms of dry mouth may have been a consequence of mass compression. The patient recovered without any complications and no evidence of recurrence or discomfort was observed 15 months postoperatively.</p>
</sec>
<sec sec-type="Discussion">
<title>Discussion</title>
<p>The present case study reported on a rare case of non-infiltrating angiolipoma that was confused with a ranula, as the patient had a dry mouth. Recurrence has been frequently reported in cases of the infiltrating form of the lesion (<xref rid="b4-ETM-26-3-12157" ref-type="bibr">4</xref>,<xref rid="b13-ETM-26-3-12157" ref-type="bibr">13</xref>). Histopathologic evaluation revealed fibrous encapsulated tumour formation composed of &#x003E;50&#x0025; mature lipocytes with angiomatous proliferation consisting of several small-to-medium-sized congested capillaries containing fibrin thrombi (<xref rid="b3-ETM-26-3-12157" ref-type="bibr">3</xref>,<xref rid="b14-ETM-26-3-12157" ref-type="bibr">14</xref>).</p>
<p>Infiltrating angiolipoma is more common in elderly patients; however, the patient of the present study was a rare case of non-infiltrating angiolipoma on the floor of the mouth in an elderly patient. There are various hypotheses regarding the aetiology of angiolipoma: i) History of trauma, ii) lipomatous differentiation by hormones at puberty, iii) fatty degeneration of central haemangioma, and iv) vascular proliferation of congenital lipoma (<xref rid="b15-ETM-26-3-12157" ref-type="bibr">15</xref>). Considering age, one possible aetiology is vascular proliferation on the pre-existing oral lipoma.</p>
<p>It may be enlarged, such as a &#x2018;plunging ranula&#x2019;, potentially causing airway problems if it was a ranula. Magnetic resonance imaging (MRI) is the gold standard for further differential diagnosis of the ranula. The T2-weighted images demonstrate a characteristic heterogeneously increased signal within the lesion (<xref rid="b16-ETM-26-3-12157" ref-type="bibr">16</xref>). However, if the ranula has a high protein concentration, the signal intensities may be high for all of the imaging sequences (<xref rid="b16-ETM-26-3-12157" ref-type="bibr">16</xref>). In such cases, a differential diagnosis of lipomas is difficult (<xref rid="b17-ETM-26-3-12157" ref-type="bibr">17</xref>). The relatively high cost of MRI must also be considered. In addition, if the lesion shows a prominent arterial supply on angiography, it is a candidate for preoperative embolization (<xref rid="b18-ETM-26-3-12157" ref-type="bibr">18</xref>).</p>
<p>Marsupialisation has been reported for the management of ranula, odontogenic cysts (odontogenic keratocyst) and benign odontogenic tumours (ameloblastoma followed by enucleation). However, the recurrence rate continues to be of concern (14-67, 12 and 29.3&#x0025;, respectively) (<xref rid="b19-ETM-26-3-12157" ref-type="bibr">19</xref>,<xref rid="b20-ETM-26-3-12157" ref-type="bibr">20</xref>). In marsupialisation, the cyst lining is sutured to the oral mucosa and the mouth floor is reconstructed. However, in the present study, the mass was resected, including the capsule and the overlying mucosa. This enables pathological diagnosis and may reduce the possibility of recurrence without any additional surgery. Circumferential tissue was used to approximate and reconstruct the floor of the mouth and the wound was healed by secondary intention.</p>
<p>In the literature, the overall prognosis for these lesions is good, as no malignant transformation has been reported (<xref rid="b4-ETM-26-3-12157" ref-type="bibr">4</xref>,<xref rid="b21-ETM-26-3-12157" ref-type="bibr">21</xref>). However, these benign tumours do not spontaneously regress and may become larger, more tender and more disfiguring (<xref rid="b9-ETM-26-3-12157" ref-type="bibr">9</xref>,<xref rid="b21-ETM-26-3-12157" ref-type="bibr">21</xref>). In addition, as there is a higher incidence of infiltrating angiolipoma, definite treatment should be considered in elderly patients.</p>
<p>In conclusion, as non-infiltrating angiolipoma of the floor of the mouth in an elderly patient is a rare pathology, it is important to diagnose the lesion exactly and treat it by intraoral approach without the possibility of complications.</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>All data generated or analyzed during this study are included in this published article.</p>
</sec>
<sec>
<title>Authors&#x0027; contributions</title>
<p>YJK and SGK performed the surgical treatment. Pathological examination and diagnosis was performed by SSL. Additional pathological analysis and literature review was completed by YJK and SGK. YJK wrote the manuscript. SSL and SGK confirm the authenticity of all the raw data. SGK supervised the study. All authors have read and approved the final version of the manuscript.</p>
</sec>
<sec>
<title>Ethics approval and consent to participate</title>
<p>This study was approved by the IRB of Gangneung-Wonju National University Dental Hospital (Gangneung, Korea; no. GWNUDH-IRB2022-A013).</p>
</sec>
<sec>
<title>Patient consent for publication</title>
<p>Not applicable.</p>
</sec>
<sec sec-type="COI-statement">
<title>Competing interests</title>
<p>The authors declare that they have no competing interests.</p>
</sec>
<ref-list>
<title>References</title>
<ref id="b1-ETM-26-3-12157"><label>1</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Chandrasekaran</surname><given-names>D</given-names></name><name><surname>Chinnaswami</surname><given-names>R</given-names></name><name><surname>Narasimhan</surname><given-names>M</given-names></name><name><surname>Kumar</surname><given-names>AEN</given-names></name><name><surname>Natarajan</surname><given-names>P</given-names></name></person-group><article-title>Non infiltrating angiolipoma of the palate in geriatric patient: A case report with review of literature</article-title><source>J Clin Diagn Res</source><volume>10</volume><fpage>ZD01</fpage><lpage>ZD02</lpage><year>2016</year><pub-id pub-id-type="pmid">27014643</pub-id><pub-id pub-id-type="doi">10.7860/JCDR/2016/16634.7032</pub-id></element-citation></ref>
<ref id="b2-ETM-26-3-12157"><label>2</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Hoeft</surname><given-names>S</given-names></name><name><surname>Luettges</surname><given-names>J</given-names></name><name><surname>Werner</surname><given-names>JA</given-names></name></person-group><article-title>Infiltrating angiolipoma of the M. temporalis</article-title><source>Auris Nasus Larynx</source><volume>27</volume><fpage>265</fpage><lpage>269</lpage><year>2000</year><pub-id pub-id-type="pmid">10808117</pub-id><pub-id pub-id-type="doi">10.1016/s0385-8146(99)00075-9</pub-id></element-citation></ref>
<ref id="b3-ETM-26-3-12157"><label>3</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Silva-Junior</surname><given-names>GO</given-names></name><name><surname>Picciani</surname><given-names>BL</given-names></name><name><surname>Costa</surname><given-names>RC</given-names></name><name><surname>Barbosa</surname><given-names>SM</given-names></name><name><surname>Silvares</surname><given-names>MG</given-names></name><name><surname>Souza</surname><given-names>RB</given-names></name><name><surname>Cantisano</surname><given-names>MH</given-names></name><name><surname>Pires</surname><given-names>FR</given-names></name></person-group><article-title>Oral soft-tissue angiolipoma: Report of two cases of rare oral lipomatous lesion with emphasis on morphological and immunohistochemical features</article-title><source>J Oral Sci</source><volume>55</volume><fpage>85</fpage><lpage>88</lpage><year>2013</year><pub-id pub-id-type="pmid">23485606</pub-id><pub-id pub-id-type="doi">10.2334/josnusd.55.85</pub-id></element-citation></ref>
<ref id="b4-ETM-26-3-12157"><label>4</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Yanase</surname><given-names>S</given-names></name><name><surname>Nomura</surname><given-names>J</given-names></name><name><surname>Matsumura</surname><given-names>Y</given-names></name><name><surname>Kato</surname><given-names>H</given-names></name><name><surname>Takeoka</surname><given-names>T</given-names></name><name><surname>Imura</surname><given-names>H</given-names></name><name><surname>Matsuura</surname><given-names>R</given-names></name><name><surname>Nakanishi</surname><given-names>K</given-names></name><name><surname>Tagawa</surname><given-names>T</given-names></name></person-group><article-title>Angiolipoma of the cheek: A case report with a literature review</article-title><source>Asian J Oral Maxillofac Surg</source><volume>23</volume><fpage>35</fpage><lpage>37</lpage><year>2011</year></element-citation></ref>
<ref id="b5-ETM-26-3-12157"><label>5</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Saydam</surname><given-names>L</given-names></name><name><surname>Bozkurt</surname><given-names>MK</given-names></name><name><surname>Ugur</surname><given-names>MB</given-names></name><name><surname>Ozcelik</surname><given-names>T</given-names></name><name><surname>Kutluay</surname><given-names>L</given-names></name></person-group><article-title>Angiolipoma of the neck: A case report</article-title><source>Ear Nose Throat J</source><volume>84</volume><fpage>375</fpage><lpage>377</lpage><year>2005</year><pub-id pub-id-type="pmid">16075864</pub-id></element-citation></ref>
<ref id="b6-ETM-26-3-12157"><label>6</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Auo</surname><given-names>HJ</given-names></name><name><surname>Kang</surname><given-names>JM</given-names></name></person-group><article-title>Infiltrating angiolipoma of the nasopharynx: Adjacent to an aberrant internal carotid artery</article-title><source>Auris Nasus Larynx</source><volume>36</volume><fpage>247</fpage><lpage>250</lpage><year>2009</year><pub-id pub-id-type="pmid">18602235</pub-id><pub-id pub-id-type="doi">10.1016/j.anl.2008.05.004</pub-id></element-citation></ref>
<ref id="b7-ETM-26-3-12157"><label>7</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Lin</surname><given-names>JJ</given-names></name><name><surname>Lin</surname><given-names>F</given-names></name></person-group><article-title>Two entities in angiolipoma. A study of 459 cases of lipoma with review of literature on infiltrating angiolipoma</article-title><source>Cancer</source><volume>34</volume><fpage>720</fpage><lpage>727</lpage><year>1974</year><pub-id pub-id-type="pmid">4855281</pub-id><pub-id pub-id-type="doi">10.1002/1097-0142(197409)34:3&#x003C;720::aid-cncr2820340331&#x003E;3.0.co;2-k</pub-id></element-citation></ref>
<ref id="b8-ETM-26-3-12157"><label>8</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Gerard</surname><given-names>N</given-names></name><name><surname>Schultz</surname><given-names>DA</given-names></name></person-group><article-title>Angiolipoma of the upper lip: Report of a case</article-title><source>J Oral Maxillofac Surg</source><volume>67</volume><fpage>1340</fpage><lpage>1341</lpage><year>2009</year><pub-id pub-id-type="pmid">19446230</pub-id><pub-id pub-id-type="doi">10.1016/j.joms.2009.02.005</pub-id></element-citation></ref>
<ref id="b9-ETM-26-3-12157"><label>9</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Reiser</surname><given-names>V</given-names></name><name><surname>Haj Yahya</surname><given-names>B</given-names></name><name><surname>Chaushu</surname><given-names>G</given-names></name><name><surname>Kaplan</surname><given-names>I</given-names></name><name><surname>Hamzani</surname><given-names>Y</given-names></name></person-group><article-title>Angiolipoma in the head and neck: Imaging, diagnosis and management</article-title><source>Medicina (Kaunas)</source><volume>56</volume><issue>283</issue><year>2020</year><pub-id pub-id-type="pmid">32532063</pub-id><pub-id pub-id-type="doi">10.3390/medicina56060283</pub-id></element-citation></ref>
<ref id="b10-ETM-26-3-12157"><label>10</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Kokong</surname><given-names>D</given-names></name><name><surname>Iduh</surname><given-names>A</given-names></name><name><surname>Chukwu</surname><given-names>I</given-names></name><name><surname>Mugu</surname><given-names>J</given-names></name><name><surname>Nuhu</surname><given-names>S</given-names></name><name><surname>Augustine</surname><given-names>S</given-names></name></person-group><article-title>Ranula: Current concept of pathophysiologic basis and surgical management options</article-title><source>World J Surg</source><volume>41</volume><fpage>1476</fpage><lpage>1481</lpage><year>2017</year><pub-id pub-id-type="pmid">28194490</pub-id><pub-id pub-id-type="doi">10.1007/s00268-017-3901-2</pub-id></element-citation></ref>
<ref id="b11-ETM-26-3-12157"><label>11</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Ohnishi</surname><given-names>Y</given-names></name><name><surname>Watanabe</surname><given-names>M</given-names></name><name><surname>Fujii</surname><given-names>T</given-names></name><name><surname>Yasui</surname><given-names>H</given-names></name><name><surname>Kubo</surname><given-names>H</given-names></name><name><surname>Kakudo</surname><given-names>K</given-names></name></person-group><article-title>Infiltrating angiolipoma of the lower lip: A case report and literature review</article-title><source>Oncol Lett</source><volume>9</volume><fpage>833</fpage><lpage>836</lpage><year>2015</year><pub-id pub-id-type="pmid">25621058</pub-id><pub-id pub-id-type="doi">10.3892/ol.2014.2737</pub-id></element-citation></ref>
<ref id="b12-ETM-26-3-12157"><label>12</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Hemavathy</surname><given-names>S</given-names></name><name><surname>Roy</surname><given-names>S</given-names></name><name><surname>Kiresur</surname><given-names>A</given-names></name></person-group><article-title>Intraosseous angiolipoma of the mandible</article-title><source>J Oral Maxillofac Pathol</source><volume>16</volume><fpage>283</fpage><lpage>287</lpage><year>2012</year><pub-id pub-id-type="pmid">22923906</pub-id><pub-id pub-id-type="doi">10.4103/0973-029X.99091</pub-id></element-citation></ref>
<ref id="b13-ETM-26-3-12157"><label>13</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Flaggert</surname><given-names>JJ III</given-names></name><name><surname>Heldt</surname><given-names>LV</given-names></name><name><surname>Keaton</surname><given-names>WM</given-names></name></person-group><article-title>Angiolipoma of the palate: Report of a case</article-title><source>Oral Surg Oral Med Oral Pathol</source><volume>61</volume><fpage>333</fpage><lpage>336</lpage><year>1986</year><pub-id pub-id-type="pmid">3458142</pub-id><pub-id pub-id-type="doi">10.1016/0030-4220(86)90412-3</pub-id></element-citation></ref>
<ref id="b14-ETM-26-3-12157"><label>14</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Shah</surname><given-names>VS</given-names></name><name><surname>Harish</surname><given-names>M</given-names></name><name><surname>Patel</surname><given-names>JR</given-names></name><name><surname>Shah</surname><given-names>N</given-names></name></person-group><article-title>Infiltrating angiolipoma of the cheek</article-title><source>BMJ Case Rep</source><volume>2013</volume><issue>bcr2013200041</issue><year>2013</year><pub-id pub-id-type="pmid">24014331</pub-id><pub-id pub-id-type="doi">10.1136/bcr-2013-200041</pub-id></element-citation></ref>
<ref id="b15-ETM-26-3-12157"><label>15</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Palaia</surname><given-names>G</given-names></name><name><surname>Gaimari</surname><given-names>G</given-names></name><name><surname>Giudice</surname><given-names>RL</given-names></name><name><surname>Galanakis</surname><given-names>A</given-names></name><name><surname>Tenore</surname><given-names>G</given-names></name><name><surname>Romeo</surname><given-names>U</given-names></name></person-group><article-title>Excision of an oral angiolipoma by KTP laser: A case report</article-title><source>Ann Stomatol (Roma)</source><volume>2</volume><fpage>28</fpage><lpage>31</lpage><year>2011</year><pub-id pub-id-type="pmid">22238720</pub-id></element-citation></ref>
<ref id="b16-ETM-26-3-12157"><label>16</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Gupta</surname><given-names>A</given-names></name><name><surname>Karjodkar</surname><given-names>F</given-names></name></person-group><article-title>Plunging ranula: A case report</article-title><source>ISRN Dent</source><volume>2011</volume><issue>806928</issue><year>2011</year><pub-id pub-id-type="pmid">21991487</pub-id><pub-id pub-id-type="doi">10.5402/2011/806928</pub-id></element-citation></ref>
<ref id="b17-ETM-26-3-12157"><label>17</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Brandwein</surname><given-names>M</given-names></name><name><surname>Som</surname><given-names>P</given-names></name></person-group><comment>Salivary glands: Anatomy and pathology. In: Som RM, Curtin HD (eds). Head and Neck Imaging, 4th edition. St. Louis, MO: Mosby, pp2039-2050, 2003.</comment></element-citation></ref>
<ref id="b18-ETM-26-3-12157"><label>18</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Rabin</surname><given-names>D</given-names></name><name><surname>Hon</surname><given-names>BA</given-names></name><name><surname>Pelz</surname><given-names>DM</given-names></name><name><surname>Ang</surname><given-names>LC</given-names></name><name><surname>Lee</surname><given-names>DH</given-names></name><name><surname>Duggal</surname><given-names>N</given-names></name></person-group><article-title>Infiltrating spinal angiolipoma: A case report and review of the literature</article-title><source>J Spinal Disord Tech</source><volume>17</volume><fpage>456</fpage><lpage>461</lpage><year>2004</year><pub-id pub-id-type="pmid">15385889</pub-id><pub-id pub-id-type="doi">10.1097/01.bsd.0000109834.59382.d5</pub-id></element-citation></ref>
<ref id="b19-ETM-26-3-12157"><label>19</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Hong</surname><given-names>J</given-names></name><name><surname>Yun</surname><given-names>PY</given-names></name><name><surname>Chung</surname><given-names>IH</given-names></name><name><surname>Myoung</surname><given-names>H</given-names></name><name><surname>Suh</surname><given-names>JD</given-names></name><name><surname>Seo</surname><given-names>BM</given-names></name><name><surname>Lee</surname><given-names>JH</given-names></name><name><surname>Choung</surname><given-names>PH</given-names></name></person-group><article-title>Long-term follow up on recurrence of 305 ameloblastoma cases</article-title><source>Int J Oral Maxillofac Surg</source><volume>36</volume><fpage>283</fpage><lpage>288</lpage><year>2007</year><pub-id pub-id-type="pmid">17222535</pub-id><pub-id pub-id-type="doi">10.1016/j.ijom.2006.11.003</pub-id></element-citation></ref>
<ref id="b20-ETM-26-3-12157"><label>20</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Kademani</surname><given-names>D</given-names></name><name><surname>Tiwana</surname><given-names>P</given-names></name></person-group><comment>Atlas of oral and maxillofacial surgery. 1st edition. Elsevier Health Sciences, 2015.</comment></element-citation></ref>
<ref id="b21-ETM-26-3-12157"><label>21</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Alvi</surname><given-names>A</given-names></name><name><surname>Garner</surname><given-names>C</given-names></name><name><surname>Thomas</surname><given-names>W</given-names></name></person-group><article-title>Angiolipoma of the head and neck</article-title><source>J Otolaryngol</source><volume>27</volume><fpage>100</fpage><lpage>103</lpage><year>1998</year><pub-id pub-id-type="pmid">9572463</pub-id></element-citation></ref>
</ref-list>
</back>
<floats-group>
<fig id="f1-ETM-26-3-12157" position="float">
<label>Figure 1</label>
<caption><p>Pre-operative intra-oral view of the patient&#x0027;s condition. The lesion in question, identified as an angiolipoma, is prominently displayed (arrow). It exhibits a distinctive dome-like shape, indicative of its exophytic nature, which refers to its growth outward from the tissue surface. The apex of this lesion is specifically located at the orifice area of Wharton&#x0027;s duct, a crucial anatomical structure in the mouth floor responsible for the drainage of saliva from the submandibular glands. The visual representation aids in understanding the initial state of the lesion before any surgical intervention was performed.</p></caption>
<graphic xlink:href="etm-26-03-12157-g00.tif" />
</fig>
<fig id="f2-ETM-26-3-12157" position="float">
<label>Figure 2</label>
<caption><p>Pre-operative enhanced CT scan. (A) The scan reveals the complexity of distinguishing between a ranula and a lipoma based solely on Hounsfield units, a measure of radiodensity. The Hounsfield units for a ranula typically register around 100, while a lipoma ranges between 65 and 120. This overlap in values makes differentiation challenging. Further complicating the evaluation is the presence of artefacts resulting from the dental crown, which obstructs the clear assessment of soft tissue swelling in the mouth floor. Despite these limitations, the CT scan does not indicate any specific abnormalities in the peripheral bone tissue. (B) Of note, the scan does reveal nodal enlargement in the submandibular and submental regions. This enlargement is interpreted as a reactive lymph node, a common immune response to infection or inflammation. CT, computed tomography.</p></caption>
<graphic xlink:href="etm-26-03-12157-g01.tif" />
</fig>
<fig id="f3-ETM-26-3-12157" position="float">
<label>Figure 3</label>
<caption><p>Peri-operative intra-oral view following the surgical intervention. The surgical site in the floor of the mouth was reconstructed using circumferential tissue, a technique that involves the strategic placement of tissue to mimic the original anatomical structure. This method was employed to restore the mouth floor to its normal function and appearance. Following the procedure, the wound underwent a healing process known as secondary intention. This process allows the wound to heal naturally from the inside out, without the need for sutures or other closure methods. The image provides a visual representation of circumferential tissue used to approximate for healing by secondary intention and the successful reconstruction of the mouth floor.</p></caption>
<graphic xlink:href="etm-26-03-12157-g02.tif" />
</fig>
<fig id="f4-ETM-26-3-12157" position="float">
<label>Figure 4</label>
<caption><p>Gross appearance of the excised mass following the surgical procedure. The mass (&#x007E;3.5 cm) is characterized by a well-defined encapsulation, a protective layer that often surrounds such growths. This encapsulated lesion was carefully excised, ensuring minimal disturbance to the surrounding tissues. Along with the lesion, an adjacent tissue sample, often referred to as a &#x2018;trapdoor&#x2019; sample due to its shape and method of extraction, was also removed. Both the excised lesion and the trapdoor sample were subsequently sent for pathological examination. This step is crucial for confirming the diagnosis and understanding the nature of the lesion in greater detail.</p></caption>
<graphic xlink:href="etm-26-03-12157-g03.tif" />
</fig>
<fig id="f5-ETM-26-3-12157" position="float">
<label>Figure 5</label>
<caption><p>Pathological evaluation of the excised mass. (A) The evaluation revealed a large fibrous stroma, a connective tissue framework, encapsulating fatty tissue. Of note, this fatty tissue did not exhibit any signs of atypia, suggesting the absence of abnormal or dysplastic cells. Within this fatty tissue, a significant proliferation of capillaries was observed, indicating an active blood supply to the area (arrow). (B) These capillaries were found to contain fibrin thrombi (arrow), clots formed by fibrin proteins, and exhibited fibrofatty changes. These changes typically involve the replacement or transformation of normal tissue structures with fibrous and fatty tissues. The image provides a detailed visual representation of these pathological findings (haematoxylin and eosin stain; magnification, x100; scale bars, 100 &#x00B5;m).</p></caption>
<graphic xlink:href="etm-26-03-12157-g04.tif" />
</fig>
</floats-group>
</article>
