<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJEM</journal-id><journal-title-group><journal-title>Open Journal of Emergency Medicine</journal-title></journal-title-group><issn pub-type="epub">2332-1806</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojem.2021.92005</article-id><article-id pub-id-type="publisher-id">OJEM-109761</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Giant Lipoma of the Cheek: A Case Report
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Dahi</surname><given-names>Mohamed El Moctar</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ahmedou</surname><given-names>Moulaye Idriss</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Tfeil</surname><given-names>Yahya</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Lamine</surname><given-names>Keita</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mariem</surname><given-names>Aziza Sass</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Abdel</surname><given-names>Moumine</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Cheich</surname><given-names>Sidi</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Abdellahi</surname><given-names>Deddy</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ladour</surname><given-names>Abd El Vetah</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Service ORL, Centre Hospitalier National, Nouakchott, Mauritanie</addr-line></aff><aff id="aff2"><addr-line>Surgery Department Faculty of Medicine UNA, Nouakchott, Mauritanie</addr-line></aff><pub-date pub-type="epub"><day>14</day><month>04</month><year>2021</year></pub-date><volume>09</volume><issue>02</issue><fpage>32</fpage><lpage>39</lpage><history><date date-type="received"><day>5,</day>	<month>April</month>	<year>2021</year></date><date date-type="rev-recd"><day>6,</day>	<month>June</month>	<year>2021</year>	</date><date date-type="accepted"><day>9,</day>	<month>June</month>	<year>2021</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Lipomas are the most common fatty mesenchymal tumors in the human body. They are very rare in the oral cavity. With a predilection, they have a rate of 1% to 4%. We report the case of a 74-year-old woman with a large painless lump on the left cheek of the mouth. This mass invading the deep spaces of the face induced a more difficult surgical excision.
 
</p></abstract><kwd-group><kwd>Lipoma</kwd><kwd> Giant</kwd><kwd> Cheek</kwd><kwd> Mauritania</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Lipomas are among the most common benign mesenchymal tumors in humans, which can occur in any region of the human body [<xref ref-type="bibr" rid="scirp.109761-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.109761-ref2">2</xref>]. They usually occur in the head and neck area; however, in the oral cavity, they are rare with 1% to 4% of all benign oral tumors [<xref ref-type="bibr" rid="scirp.109761-ref3">3</xref>]. These tumors are usually surrounded by a connective tissue capsule and often rest on a large pedicle; their growth is slow and painless, and their yellow color is sometimes visible through the mucosa when it is tight [<xref ref-type="bibr" rid="scirp.109761-ref4">4</xref>]. It has an incidence rate of about 1% - 4% of all benign oral lesions, with a prevalence rate of about 0.0002%. Specific anatomic locations of occurrence within the oral and maxillofacial region include the parotid region, buccal mucosa, lips, submandibular region, tongue, floor of the mouth, and palate [<xref ref-type="bibr" rid="scirp.109761-ref3">3</xref>]. Here we report the case of a 74-year-old patient who presented with a giant lipoma of the left cheek. She was operated on in the ENT and head and neck surgery department of the CHN in Nouakchott, Mauritania.</p></sec><sec id="s2"><title>2. Presentation of the Case</title><p>This is a 74-year-old woman, received at the consultation of the Otorhinolaryngology and Cervico-Facial Surgery Department of the National Hospital Center of Nouakchott for swelling of the left cheek of the mouth that has been evolving for more than 8 years old.</p><p>The known diabetic patient followed and treated with insulin, mainly bothered by a large painless mass. Mass localized to the left cheek of the mouth, gradually increasing in size caused discomfort during chewing and talking. In addition, the patient also complained of tension in this region of the left cheek without paresthesia.</p><p>The sociodemograpic and clinical characteristics are summarized in <xref ref-type="table" rid="table1">Table 1</xref>.</p><p>On palpation, the mass was mobile from side to side and it was elastic, dense, painless, non-adherent to the cutaneous plane and with an extension to the level of the left temporal region, and measuring 20 cm &#215; 15 cm, ranging from the lower edge of the left mandible to 1 cm in front of the left ear (<xref ref-type="fig" rid="fig1">Figure 1</xref>(a) and <xref ref-type="fig" rid="fig1">Figure 1</xref>(b)).</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Sociodemographic and clinical characteristics</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Item</th><th align="center" valign="middle"  colspan="2"  >Result</th></tr></thead><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle"  colspan="2"  >74 years</td></tr><tr><td align="center" valign="middle" >Sex</td><td align="center" valign="middle"  colspan="2"  >Female</td></tr><tr><td align="center" valign="middle" >Socioeconomic level</td><td align="center" valign="middle"  colspan="2"  >poor</td></tr><tr><td align="center" valign="middle" >Signs</td><td align="center" valign="middle" >Preoperatory</td><td align="center" valign="middle" >Postoperatory</td></tr><tr><td align="center" valign="middle" >Trismus</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Dysphagia</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Disarticulation</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Facial dysmorphism</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr></tbody></table></table-wrap><p>On the oral examination, the mass was palpable and non-fluctuating with a normal appearance of the mucosa opposite. The remainder of the ENT exam was unremarkable.</p><p>Facial Computed tomography found a voluminous fatty mass of the left face, with thin, regular boundaries enhanced after injection of contrast product and measuring 20 cm &#215; 13 cm &#215; 9 cm. It extended to the infra-temporal and pterygomaxillary fossa, compressing the ipsilateral masticatory muscle, pushing the left pterygoid muscle and the left parotid gland posteriorly (<xref ref-type="fig" rid="fig2">Figure 2</xref>).</p><p>The mass was removed under general anesthesia through a horizontal incision of 10cm in the length going with the major axis of the mass (<xref ref-type="fig" rid="fig3">Figure 3</xref>). Detachment of the upper and lower flaps was easy. The pathological tissue demonstrated was surrounded by a thin connective capsule and its coloration was distinctly yellow after the opening of the fascia, clearly differentiating from the surrounding tissue structures (<xref ref-type="fig" rid="fig4">Figure 4</xref>). The lesion was easily separated from the adjacent tissue. Following the cleavage plane, the mass has easily dissected from the infra-temporal and pterygopalatine fossae and ends in the pterygopalatine fossa (<xref ref-type="fig" rid="fig5">Figure 5</xref>(a) and <xref ref-type="fig" rid="fig5">Figure 5</xref>(b)). The arterial blood supply was from the pterygomaxillary artery and separated from the lesion by electro coagulation with bipolar forceps. The excision of the pterygopalatine part was difficult; a slight hemorrhage had occurred but was controlled a time by compression. The removal of the temporal part was performed through a second incision in the temporal region.</p><p>The surgical specimen removed, with a smooth and well-defined surface, measured 20 cm and showed clearly visible lobules and septa (<xref ref-type="fig" rid="fig6">Figure 6</xref>). Postoperative closure was achieved by separate stitches without remodeling</p><p>During the postoperative phase, the patient received antibiotic coverage for ten days (amoxicillin-clavulanic acid combination); analgesic treatment was provided by paracetamol. Wound disinfection was performed with 10% povidone iodine solution every other day.</p><p>Outcome and follow-up:</p><p>There were no postoperative complications. The patient was discharged after placing sutures and was called after a week for the removal of the sutures (<xref ref-type="fig" rid="fig7">Figure 7</xref>).</p><p>The patient was reviewed 6 weeks later and the clinical evaluation noted complete resolution of symptoms (<xref ref-type="table" rid="table1">Table 1</xref>).</p><p>The histo-pathological examination of the mass concluded the presence purely fatty tissue with normal excisional limits.</p></sec><sec id="s3"><title>3. Discussion</title><p>Lipomas are the benign tumor of mature adipose tissue. Near 20% are seen in the head and neck region and only 1% to 4% involve the oral cavity [<xref ref-type="bibr" rid="scirp.109761-ref3">3</xref>]. They affect individuals in the 4th - 6th decades, the size rarely exceeds 25 mm [<xref ref-type="bibr" rid="scirp.109761-ref5">5</xref>], and has a slight male predilection [<xref ref-type="bibr" rid="scirp.109761-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.109761-ref6">6</xref>]. A few studies have reported an equal distribution between the sexes [<xref ref-type="bibr" rid="scirp.109761-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.109761-ref8">8</xref>]. In addition, a case of cellular angiolipoma infiltrating the cheek in a 9 months old infant has been reported [<xref ref-type="bibr" rid="scirp.109761-ref9">9</xref>]. Clinically, intraoral lipomas are generally slowed growing and asymptomatic. However, few reports associate intraoral lipomas with dysphagia and dyspnea apart from speech and chewing problems depending on size and anatomical location [<xref ref-type="bibr" rid="scirp.109761-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.109761-ref11">11</xref>]. In this case, the patient had noticed the swelling of the left cheek eight years previously but had not consulted. However, she developed difficulties with chewing and speaking, which led to her seeking treatment. According to Park BG et al, the time during which the patient notices a lipoma to see a doctor varies from 1 month to 10 years, with an average of 2 years [<xref ref-type="bibr" rid="scirp.109761-ref12">12</xref>]. It is the indolence and lack of functional impairment that are at the origin of such impressive tumors encountered so far in our underdeveloped countries. A similar CT scan has been reported [<xref ref-type="bibr" rid="scirp.109761-ref13">13</xref>] with the addition of an extension towards the right parapharyngeal space causing narrowing of the airways at this level. If the tumor engulfs the Stenon duct, it may be symptomatic, leading to recurrent parotid sialadenitis [<xref ref-type="bibr" rid="scirp.109761-ref14">14</xref>]. In our patient the Stenon canal was not swallowed up; however, the left parotid gland was pushed back.</p><p>Histologically, lipomas consist of mature adipocytes grouped together in bundles with a clear cytoplasm and an eccentric nucleus separated by connective septa [<xref ref-type="bibr" rid="scirp.109761-ref15">15</xref>]. Although rare, malignant transformation of the lipoma has also been reported [<xref ref-type="bibr" rid="scirp.109761-ref16">16</xref>]. The pathological result, in our case, is in favor of a simple lipoma.</p><p>The treatment of choice for lipoma is surgical excision; however, removal can be difficult in situations if they are positioned deep [<xref ref-type="bibr" rid="scirp.109761-ref17">17</xref>], or the hidden part of the iceberg, represented by fatty extensions in the deep spaces of the face. In our patient, the excision was laborious because of the extensions at the level of the pterygomaxillary, pterygopalatine, and infra-temporal fossae. In plastic surgery, liposuction is mainly used for large lipomas (&#216; &gt; 4 cm) with superficial localization [<xref ref-type="bibr" rid="scirp.109761-ref18">18</xref>]. The advantages of this technique are as follows: the patients are satisfied due to the limited postoperative complications and the esthetic results are excellent, due to the minimal scarring. However, this technique finds its limits when it comes to excising fibroid lipomas, as it often results in incomplete excision of the tumor [<xref ref-type="bibr" rid="scirp.109761-ref19">19</xref>].</p><p>Recurrences or complications after surgical removal are rare [<xref ref-type="bibr" rid="scirp.109761-ref12">12</xref>] as also observed in the present case at 45 days of follow-up with good speech, conversation, and chewing.</p></sec><sec id="s4"><title>4. Conclusion</title><p>Lipomas are benign, painless, slow-growing, ubiquitous tumors, but their oral location is rare. Depending on their size, they can cause aesthetic and/or functional problems. Surgical excision remains the treatment of choice for this lesion.</p></sec><sec id="s5"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s6"><title>Cite this paper</title><p>El Moctar, D.M., Idriss, A.M., Yahya, T., Keita, L., Sass, M.A., Moumine, A., Sidi, C., Deddy, A. and El Vetah, L.A. (2021) Giant Lipoma of the Cheek: A Case Report. Open Journal of Emergency Medicine, 9, 32-39. https://doi.org/10.4236/ojem.2021.92005</p></sec></body><back><ref-list><title>References</title><ref id="scirp.109761-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Basheer, S., Abraham, J., Shameena, P., et al. (2013) Intraosseous Lipoma of Mandible Presenting as a Swelling. 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