<?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">OJPathology</journal-id><journal-title-group><journal-title>Open Journal of Pathology</journal-title></journal-title-group><issn pub-type="epub">2164-6775</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojpathology.2014.43013</article-id><article-id pub-id-type="publisher-id">OJPathology-47662</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>Hamartomatous Polyp of Minor Salivary Gland Arising in the Tongue: A Report of the First Case</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yosep</surname><given-names>Chong</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>Young</surname><given-names>Hak Park</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>Tae-Jung</surname><given-names>Kim</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>Chang</surname><given-names>Suk Kang</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Hospital Pathology, Yeouido St. Mary’s Hospital, The Catholic University of Korea College of Medicine, Seoul, South Korea</addr-line></aff><aff id="aff2"><addr-line>Department of Otolaryngology-Head and Neck Surgery, Yeouido St. Mary’s Hospital, The Catholic University of Korea College of Medicine, Seoul, South Korea</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>cskang@catholic.ac.kr(CSK)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>09</day><month>07</month><year>2014</year></pub-date><volume>04</volume><issue>03</issue><fpage>83</fpage><lpage>85</lpage><history><date date-type="received"><day>15</day>	<month>April</month>	<year>2014</year></date><date date-type="rev-recd"><day>15</day>	<month>May</month>	<year>2014</year>	</date><date date-type="accepted"><day>5</day>	<month>June</month>	<year>2014</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>
	Benign tumorous condition can
be encountered at very unusual location in oral cavity and pharyngeal region,
which leads diagnostic difficulty. Here we describe a very unusual presentation
of polypoid hamartoma on the root of the tongue. A 59-year-old woman presented
with a polypoid tumor mass on the dorsal root of the tongue. Microscopically,
it was hamartoma showing normal salivary glands of mucinous and serous types,
lymphoid hyperplasia, and skeletal muscle bundles. Major differential diagnoses
include accessory tongue, adenomatoid hyperplasia, and idiopathic hyperplasia
of sublingual glands. To our knowledge, this is the first report of hamartoma
arising in the root of the tongue presenting as polypoid mass. Correct
diagnosis based on pathologic examination is essential for proper treatment. 
</p></abstract><kwd-group><kwd>Hamartoma</kwd><kwd> Minor Salivary Gland</kwd><kwd> Tongue Neoplasm</kwd><kwd> Polyps</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Various soft-tissue lesions of the oral cavity that present as tumors are commonly observed in daily practice. Such benign lesions include irritation fibroma, peripheral ossifying fibroma, pyogenic granuloma, peripheral giant-cell granuloma, salivary gland choristoma, granular cell tumor, verruciform xanthoma, hairy polyp, and mesenchymal tumors such as leiomyoma, rhabdomyoma, schwannoma, neurofibroma, traumatic neuroma, lipoma, hemangioma, and solitary fibrous tumor [<xref ref-type="bibr" rid="scirp.47662-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.47662-ref2">2</xref>] . In addition, adenomatoid hyperplasia of minor salivary glands, idiopathic hyperplasia of sublingual glands, and various types of malignant lymphoma can also present as polypoid tumor-like lesions [<xref ref-type="bibr" rid="scirp.47662-ref3">3</xref>] -[<xref ref-type="bibr" rid="scirp.47662-ref5">5</xref>] .</p><p>Recently, we experienced a very unusual hamartomatous lesion of the minor salivary gland presenting as a pedunculated polyp on the base of the tongue in a 59-year-old woman. To the best of our knowledge, such a case has not previously been reported. Here, we present the case with a brief review of the current literature.</p></sec><sec id="s2"><title>2. Case Presentation</title><p>A 59-year-old woman presented with a polypoid mass on the dorsal root of the tongue. She did not complain of pain or tenderness but had a little difficulty swallowing. She had no history of local trauma in the oral cavity such as dental extraction surgery.</p><p>On laryngoscopic examination, the mass was a 1.5 &#215; 1.2-cm pedunculated polypoid mass with normal-ap- pearing mucosa arising in the base of the tongue (<xref ref-type="fig" rid="fig1">Figure 1</xref>). The tumor was attached to the base of the tongue by a stalk and generally looked benign. The relationship of the tumor and the tongue is illustrated in <xref ref-type="fig" rid="fig1">Figure 1</xref>(B). The mass was removed under local anesthesia.</p><p>On microscopic examination, it consisted of a lobulated mass of normal salivary glands of mucinous and serous types with loose connective tissue and normal overlying mucosa. Multifocal areas of submucosal soft tissue showed lymphoid hyperplasia that could be considered part of the lingual tonsils. The inner region of the tumor showed skeletal muscle bundles (H&amp;E stain) (<xref ref-type="fig" rid="fig2">Figure 2</xref>).</p><p>Magnetic resonance imaging performed after surgical removal revealed no suspicious local invasion or remnant tumor in the resected area.</p></sec><sec id="s3"><title>3. Conclusions</title><p>The major differential diagnosis of this case was accessory tongue, adenomatoid hyperplasia of minor salivary glands, and tumorous presentation of idiopathic hyperplasia of sublingual glands. Tongue anomalies such as accessory tongue can be ruled out by the fact that the tumor had not been present since birth [<xref ref-type="bibr" rid="scirp.47662-ref6">6</xref>] . Although our case also had a muscular component in the core of the lesion, it was mainly composed of normal lobulated salivary glands. Adenomatoid hyperplasia of minor salivary glands could also be considered in this case. However, the salivary glands in adenomatoid hyperplasia are more hyperplastic and composed of only mucinous glands [<xref ref-type="bibr" rid="scirp.47662-ref1">1</xref>] . Furthermore, the muscular component in this case cannot be explained by adenomatoid hyperplasia. Idiopathic hyperplasia of sublingual glands can also present as a tumorous lesion; however, it presents as a sessile lesion in the retromolar area and is usually associated with an edentulous condition [<xref ref-type="bibr" rid="scirp.47662-ref3">3</xref>] -[<xref ref-type="bibr" rid="scirp.47662-ref5">5</xref>] .</p></sec><sec id="s4"><title>4. Summary</title><p>Because of the anatomical complexity of head and neck region, benign conditions mimicking tumor can be easily</p><fig id="fig1"><label>Figure 1</label><caption><p> Laryngoscopic finding and graphic illustration. (A) An ovoid polypoid mass is noted on the right dorsal surface of the tongue base (arrowhead). The stalk of the mass is indicated by an arrow. Note the circumvallate papillae on the tongue base (U; uvula, T; tongue). (B) Illustration of the polypoid mass showing its relationship to the tongue</p></caption><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://file.scirp.org/Html/htmlimages\1-1940128x\a149a354-ca69-4ee2-871c-b523cb39d0c2.png"/></fig><fig id="fig2"><label>Figure 2</label><caption><p> Microscopic findings. (A) Scan power view reveals a polypoid mass with relatively intact normal-appearing mucosa. (B) The medium magnification shows well-lobulated salivary glands, intermingled skeletal muscle bundles (arrows), focal lymphoid hyperplasia, and normal-appearing mucosa. (C) Salivary glands consisting of both serous and mucinous glands are lobulated by thin fibrous bands as seen in normal minor salivary glands. (D) The submucosal connective tissue layer reveals lymphoid hyperplasia that can be found in the normal tongue base</p></caption><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://file.scirp.org/Html/htmlimages\1-1940128x\8e02ea2f-fdec-4dbc-8968-48fcee6f0047.png"/></fig><p>encountered in daily practice. However, hamartoma of minor salivary gland has never been described, and its polypoid presentation is even weirder thing. Although the histologic feature of this lesion favors benign clinical behavior, careful diagnostic workup and differential diagnosis are essential. In future, more cases should be collected to elucidate the etiology and true nature of this lesion.</p></sec></body><back><ref-list><title>References</title><ref id="scirp.47662-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">GNEPP, D.R. 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