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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">An unusual case of disappearing bone disease in the mandible and literature review</title><author><name sortKey="Naqvi, Ambareen A" sort="Naqvi, Ambareen A" uniqKey="Naqvi A" first="Ambareen A." last="Naqvi">Ambareen A. Naqvi</name><affiliation><nlm:aff id="rjx025af1"><addr-line>Oral Surgery Department, Eastman Dental Hospital, London, UK</addr-line></nlm:aff></affiliation></author><author><name sortKey="Joshi, Sandeep S" sort="Joshi, Sandeep S" uniqKey="Joshi S" first="Sandeep S." last="Joshi">Sandeep S. Joshi</name><affiliation><nlm:aff id="rjx025af1"><addr-line>Oral Surgery Department, Eastman Dental Hospital, London, UK</addr-line></nlm:aff></affiliation></author><author><name sortKey="Bailey, Edmund" sort="Bailey, Edmund" uniqKey="Bailey E" first="Edmund" last="Bailey">Edmund Bailey</name><affiliation><nlm:aff id="rjx025af1"><addr-line>Oral Surgery Department, Eastman Dental Hospital, London, UK</addr-line></nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">28878876</idno><idno type="pmc">5577639</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577639</idno><idno type="RBID">PMC:5577639</idno><idno type="doi">10.1093/jscr/rjx025</idno><date when="2017">2017</date><idno type="wicri:Area/Pmc/Corpus">001F24</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001F24</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">An unusual case of disappearing bone disease in the mandible and literature review</title><author><name sortKey="Naqvi, Ambareen A" sort="Naqvi, Ambareen A" uniqKey="Naqvi A" first="Ambareen A." last="Naqvi">Ambareen A. Naqvi</name><affiliation><nlm:aff id="rjx025af1"><addr-line>Oral Surgery Department, Eastman Dental Hospital, London, UK</addr-line></nlm:aff></affiliation></author><author><name sortKey="Joshi, Sandeep S" sort="Joshi, Sandeep S" uniqKey="Joshi S" first="Sandeep S." last="Joshi">Sandeep S. Joshi</name><affiliation><nlm:aff id="rjx025af1"><addr-line>Oral Surgery Department, Eastman Dental Hospital, London, UK</addr-line></nlm:aff></affiliation></author><author><name sortKey="Bailey, Edmund" sort="Bailey, Edmund" uniqKey="Bailey E" first="Edmund" last="Bailey">Edmund Bailey</name><affiliation><nlm:aff id="rjx025af1"><addr-line>Oral Surgery Department, Eastman Dental Hospital, London, UK</addr-line></nlm:aff></affiliation></author></analytic><series><title level="j">Journal of Surgical Case Reports</title><idno type="eISSN">2042-8812</idno><imprint><date when="2017">2017</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><title>Abstract</title><p>Disappearing bone disease is a rare disorder that causes spontaneous and progressive osteolysis and proliferation of lymphatic tissue and blood vessels. It is debilitating and there is evidence of mortality in reported cases including those affecting mandible. A 38-year-old man was diagnosed with disappearing bone disease of the mandible in 2013. This had progressed from being in the right ramus only, and now extends to the lower right first molar and affects the left coronoid process and ramus. Mandibular involvement has shown to be high-risk. In older patients, misdiagnosis can occur without thorough investigation, and education of clinicians needs to be paramount to provide the appropriate treatment for this rare condition. The disease can be debilitating and as such education and support of patients is essential.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Romer, O" uniqKey="Romer O">O Romer</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Ng, Ses" uniqKey="Ng S">SES Ng</name></author><author><name sortKey="Wang, Yt" uniqKey="Wang Y">YT Wang</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Yoshiaki, K" uniqKey="Yoshiaki K">K Yoshiaki</name></author><author><name sortKey="Koji, Y" uniqKey="Koji Y">Y Koji</name></author><author><name sortKey="Kazuaki, T" uniqKey="Kazuaki T">T Kazuaki</name></author><author><name sortKey="Keiji, T" uniqKey="Keiji T">T Keiji</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zeller, Lh" uniqKey="Zeller L">LH Zeller</name></author><author><name sortKey="Hohenberg, G" uniqKey="Hohenberg G">G Hohenberg</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Motamedi, Mhk" uniqKey="Motamedi M">MHK Motamedi</name></author><author><name sortKey="Homauni, Sm" uniqKey="Homauni S">SM Homauni</name></author><author><name sortKey="Behnia, H" uniqKey="Behnia H">H Behnia</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Mignogna, Md" uniqKey="Mignogna M">MD Mignogna</name></author><author><name sortKey="Fedele, S" uniqKey="Fedele S">S Fedele</name></author><author><name sortKey="Lo Russo, L" uniqKey="Lo Russo L">L Lo Russo</name></author><author><name sortKey="Ciccarelli, R" uniqKey="Ciccarelli R">R Ciccarelli</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Croucher, P" uniqKey="Croucher P">P Croucher</name></author><author><name sortKey="Jagdev, S" uniqKey="Jagdev S">S Jagdev</name></author><author><name sortKey="Coleman, R" uniqKey="Coleman R">R Coleman</name></author></analytic></biblStruct><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Phelan, M" uniqKey="Phelan M">M Phelan</name></author><author><name sortKey="Dobbs, J" uniqKey="Dobbs J">J Dobbs</name></author><author><name sortKey="David, As" uniqKey="David A">AS David</name></author></analytic></biblStruct></listBibl></div1></back></TEI><pmc article-type="case-report"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">J Surg Case Rep</journal-id><journal-id journal-id-type="iso-abbrev">J Surg Case Rep</journal-id><journal-id journal-id-type="publisher-id">jscr</journal-id><journal-title-group><journal-title>Journal of Surgical Case Reports</journal-title></journal-title-group><issn pub-type="epub">2042-8812</issn><publisher><publisher-name>Oxford University Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">28878876</article-id><article-id pub-id-type="pmc">5577639</article-id><article-id pub-id-type="doi">10.1093/jscr/rjx025</article-id><article-id pub-id-type="publisher-id">rjx025</article-id><article-categories><subj-group subj-group-type="heading"><subject>Case Report</subject></subj-group></article-categories><title-group><article-title>An unusual case of disappearing bone disease in the mandible and literature review</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name><surname>Naqvi</surname><given-names>Ambareen A.</given-names></name><xref ref-type="corresp" rid="rjx025cor1"></xref><xref ref-type="aff" rid="rjx025af1">1</xref><pmc-comment>ambareen.naqvi@gmail.com </pmc-comment>
</contrib><contrib contrib-type="author"><name><surname>Joshi</surname><given-names>Sandeep S.</given-names></name><xref ref-type="aff" rid="rjx025af1">1</xref></contrib><contrib contrib-type="author"><name><surname>Bailey</surname><given-names>Edmund</given-names></name><xref ref-type="aff" rid="rjx025af1">1</xref></contrib></contrib-group><aff id="rjx025af1"><label>1</label><addr-line>Oral Surgery Department, Eastman Dental Hospital, London, UK</addr-line></aff><author-notes><corresp id="rjx025cor1"><label>*</label>Correspondence address. Oral Surgery Department, Eastman Dental Hospital, 256 Gray's Inn Road, London WC1 8LD, UK. Tel: +44-2034561158; Fax: +<fax>44-2034561105</fax>; E-mail: <email>ambareen.naqvi@gmail.com</email></corresp></author-notes><pub-date pub-type="collection"><month>2</month><year>2017</year></pub-date><pub-date pub-type="epub" iso-8601-date="2017-02-23"><day>23</day><month>2</month><year>2017</year></pub-date><pub-date pub-type="pmc-release"><day>23</day><month>2</month><year>2017</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was based on the
<volume>2017</volume><issue>2</issue><elocation-id>rjx025</elocation-id><history><date date-type="received"><day>04</day><month>12</month><year>2016</year></date><date date-type="accepted"><day>09</day><month>2</month><year>2017</year></date></history><permissions><copyright-statement>Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author 2017.</copyright-statement><copyright-year>2017</copyright-year><license license-type="cc-by-nc" xlink:href="http://creativecommons.org/licenses/by-nc/4.0/"><license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (<uri xlink:href="http://creativecommons.org/licenses/by-nc/4.0/">http://creativecommons.org/licenses/by-nc/4.0/</uri>), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact <email>journals.permissions@oup.com</email></license-p></license></permissions><self-uri xlink:href="rjx025.pdf"></self-uri><abstract><title>Abstract</title><p>Disappearing bone disease is a rare disorder that causes spontaneous and progressive osteolysis and proliferation of lymphatic tissue and blood vessels. It is debilitating and there is evidence of mortality in reported cases including those affecting mandible. A 38-year-old man was diagnosed with disappearing bone disease of the mandible in 2013. This had progressed from being in the right ramus only, and now extends to the lower right first molar and affects the left coronoid process and ramus. Mandibular involvement has shown to be high-risk. In older patients, misdiagnosis can occur without thorough investigation, and education of clinicians needs to be paramount to provide the appropriate treatment for this rare condition. The disease can be debilitating and as such education and support of patients is essential.</p></abstract><counts><page-count count="2"></page-count></counts></article-meta></front><body><sec sec-type="intro" id="rjx025s4"><title>INTRODUCTION</title><p>Disappearing bone disease, or Gorham-Stout disease, is a rare disorder of unknown aetiology. Bone is progressively resorbed and replaced by lymphatic tissue [<xref rid="rjx025C1" ref-type="bibr">1</xref>]. It can involve one or more bones but it rarely affects the head and neck. The first reported case was in 1838 involving the humerus [<xref rid="rjx025C2" ref-type="bibr">2</xref>]. The first reported case in the head and neck was in 1924 [<xref rid="rjx025C2" ref-type="bibr">2</xref>].</p><p>This report presents a case of a patient with mandibular involvement diagnosed in 2013.</p></sec><sec id="rjx025s5"><title>CASE REPORT</title><p>A 38-year-old man was referred to the oral surgery department for opinion after having had some teeth removed by his dentist, which had become mobile. He had previously been seen by an oral and maxillofacial department who had diagnosed the patient with bone disappearing disease. The patient had been lost to follow up with this unit. The patient reported ‘wobbly’ teeth but no pain.</p><p>Medically, the patient had gout but was not taking any medication for this. He was a non-smoker and did not drink alcohol.</p><p>On examination, the patient was edentulous to the lower right first molar, without palpable bony tissue on this side of the mandible up until reaching the lower right first molar. There were also mobile lower teeth on this side.</p><p>On radiographic examination, there was complete bone loss of the right mandible up to the lower right first molar and also bone loss affecting the left coronoid and ramus (Fig. <xref ref-type="fig" rid="rjx025F1">1</xref>). Previous radiographic reports from 2013 had shown only bone loss of the right ramus. The patient was subsequently referred for a CT scan of his facial bones, which he failed to attend. As was the case with the previous department, he failed to attend appointments with the metabolic bone disease unit for further investigation of other bones. He was also prescribed alendronic acid, a bisphosphonate, in 2014 but did not fill the prescription.
</p><fig id="rjx025F1" fig-type="featured" orientation="portrait" position="float"><label>Figure 1:</label><caption><p>Dental panoramic tomograph from 2016 showing extensive bone loss of the right mandible, left coronoid process and ramus.</p></caption><graphic xlink:href="rjx025f01"></graphic></fig></sec><sec sec-type="discussion" id="rjx025s6"><title>DISCUSSION</title><p>Disappearing bone disease is a debilitating disease with a mortality rate of ~16% in reported cases [<xref rid="rjx025C3" ref-type="bibr">3</xref>]. Most commonly found in the pelvis, scapula, shoulder and clavicle, the mandible is the most frequently affected bone in the head and neck region [<xref rid="rjx025C4" ref-type="bibr">4</xref>].</p><p>Presentation of the disease can be a dull ache or progressive weakness. In some cases, a pathological fracture may occur. Although usually monocentric, there are reported cases of other bones being involved. Radiographic evidence was first described by Resnick, who found radiolucent foci in the initial stage leading to fracture, fragmentation and disappearance of the bone to a taper or point. Usually, there is an increase in the bony destruction with very few cases showing spontaneous recovery [<xref rid="rjx025C5" ref-type="bibr">5</xref>]. The cases of death have been usually due to bone loss in the thorax [<xref rid="rjx025C3" ref-type="bibr">3</xref>].</p><p>The disease is a locally aggressive disease with resorption of bone, proliferation of blood vessels and lymphatic tissue which can extend into the soft tissues. Histologically, there is evidence of multiple sinusoidal blood filled vessels and capillaries. Diagnosis is complicated, and a diagnostic criteria were proposed by Heffez <italic>et al</italic>.:
<list list-type="order"><list-item><p> A positive biopsy</p></list-item><list-item><p> Absence of cellular atypia</p></list-item><list-item><p> Minimal/no osteoblastic response</p></list-item><list-item><p> Evidence of local, progressive osseous resorption</p></list-item><list-item><p> Non-expansible, non-ulcerative lesion</p></list-item><list-item><p> Absence of visceral involvement</p></list-item><list-item><p> Osteolytic radiographic pattern</p></list-item><list-item><p> Negative hereditary, metabolic, neoplastic, immunologic or infectious aetiology.</p></list-item></list></p><p>At the present time, there is no recognized effective treatment. Studies have shown resection and bone grafting usually result in failure and recurrence [<xref rid="rjx025C6" ref-type="bibr">6</xref>]. Radiation therapy has been shown to be more effective but has severe side effects such as a risk of osteosarcoma in young children [<xref rid="rjx025C7" ref-type="bibr">7</xref>]. Bisphosphonates have also been shown to be more effective with newer generations such as zolendronic acid and can be used in the acute phase [<xref rid="rjx025C8" ref-type="bibr">8</xref>]. Recent evidence of osteonecrosis of the jaw from bisphosphonates highlight that this needs to be considered when prescribing it [<xref rid="rjx025C9" ref-type="bibr">9</xref>]. The risks and benefits of the treatment modality need to be assessed fully especially in patients who are polycentric.</p><p>This case, with the evidence of the morbidity and mortality associated, has emphasized the need to educate patients with regards to their condition. It is thought that some patients may be in denial with their diagnosis and as such are unwilling to go through with further investigations or treatments [<xref rid="rjx025C10" ref-type="bibr">10</xref>]. The case we have presented has shown numerous failures to attend for further investigations such as CT scans, assessment for further bony involvement and treatment.</p><p>Mobility of the teeth can be the first symptoms of the disease; hence, dentists may be the first clinician to see the patient. As well as educating the patient to the benefits of monitoring the disease and potential treatment, clinicians need to be aware that this disease can mimic periodontal disease, osteomyelitis and tumours such as giant cell tumours and as such should be aware of this as part of their differential diagnoses. It is important that these patients are referred to specialist care.</p></sec><sec sec-type="conclusions" id="rjx025s7"><title>CONCLUSION</title><p>Disappearing bone disease is a very rare but highly debilitating disease. Thorough investigation of patients needs to be performed to ensure misdiagnosis does not occur. Education of patients and clinicians is important in identifying this rare disease, and ensuring appropriate care and support is given.</p></sec></body><back><sec id="rjx025s8"><title>CONFLICT OF INTEREST STATEMENT</title><p>None declared.</p></sec><ref-list><title>REFERENCES</title><ref id="rjx025C1"><label>1</label><mixed-citation publication-type="other"><uri xlink:href="https://rarediseases.org/rare-diseases/gorham-stout-disease/">https://rarediseases.org/rare-diseases/gorham-stout-disease/</uri> (29 November 2013, date last accessed).</mixed-citation></ref><ref id="rjx025C2"><label>2</label><mixed-citation publication-type="book"><person-group person-group-type="author"><name name-style="western"><surname>Romer</surname><given-names>O</given-names></name></person-group><chapter-title>Die Pathologie der Zahne</chapter-title> In: <person-group person-group-type="editor"><name name-style="western"><surname>von Henke</surname><given-names>F</given-names></name>, <name 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