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Concomitant Factors Leading to an Atypical Osteonecrosis of the Jaw in a Patient with Multiple Myeloma

Identifieur interne : 001084 ( Ncbi/Merge ); précédent : 001083; suivant : 001085

Concomitant Factors Leading to an Atypical Osteonecrosis of the Jaw in a Patient with Multiple Myeloma

Auteurs : Jaume Miranda-Rius [Espagne] ; Lluís Brunet-Llobet [Espagne] ; Eduard Lahor-Soler [Espagne] ; Josep Anton Giménez-Rubio [Espagne]

Source :

RBID : PMC:4124701

Abstract

Osteonecrosis of the jaw (ONJ) is a site specific osseous pathology, characterized by chronic exposed bone in the mouth, which needs to be reinforced periodically within the medical literature. ONJ is a clinical entity with many possible aetiologies and its pathogenesis is not well understood. The risk factors for ONJ include bisphosphonates treatments, head and neck radiotherapy, dental procedures involving bone surgery, and trauma. Management of ONJ has centred on efforts to eliminate or reduce severity of symptoms, to slow or prevent the progression of disease, and to eradicate diseased bone. This case describes a rare case of ONJ in a 64-year-old Caucasian male diagnosed with multiple myeloma stage III. The lesion was related to a traumatic injury during mastication. Eighteen months ago in the same area the molar 37 was extracted, achieving a complete satisfactory healing, when only 2 doses of zoledronic acid had been administered. Actinomyces bacterial aggregates were also identified in the microscopic analysis. The management of this osteonecrotic lesion included antibiotic treatment and chlorhexidine topical gel administration. The evolution was monitored every two weeks until patient's death. The authors provide a discussion of the etiology, pathogenesis, diagnosis, and management. This case report may shed light on the controversies about concomitant factors and mechanisms inducing ONJ.


Url:
DOI: 10.1155/2014/281313
PubMed: 25140178
PubMed Central: 4124701

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PMC:4124701

Le document en format XML

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<p>Osteonecrosis of the jaw (ONJ) is a site specific osseous pathology, characterized by chronic exposed bone in the mouth, which needs to be reinforced periodically within the medical literature. ONJ is a clinical entity with many possible aetiologies and its pathogenesis is not well understood. The risk factors for ONJ include bisphosphonates treatments, head and neck radiotherapy, dental procedures involving bone surgery, and trauma. Management of ONJ has centred on efforts to eliminate or reduce severity of symptoms, to slow or prevent the progression of disease, and to eradicate diseased bone. This case describes a rare case of ONJ in a 64-year-old Caucasian male diagnosed with multiple myeloma stage III. The lesion was related to a traumatic injury during mastication. Eighteen months ago in the same area the molar 37 was extracted, achieving a complete satisfactory healing, when only 2 doses of zoledronic acid had been administered.
<italic>Actinomyces</italic>
bacterial aggregates were also identified in the microscopic analysis. The management of this osteonecrotic lesion included antibiotic treatment and chlorhexidine topical gel administration. The evolution was monitored every two weeks until patient's death. The authors provide a discussion of the etiology, pathogenesis, diagnosis, and management. This case report may shed light on the controversies about concomitant factors and mechanisms inducing ONJ.</p>
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</TEI>
<pmc article-type="research-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Case Rep Med</journal-id>
<journal-id journal-id-type="iso-abbrev">Case Rep Med</journal-id>
<journal-id journal-id-type="publisher-id">CRIM</journal-id>
<journal-title-group>
<journal-title>Case Reports in Medicine</journal-title>
</journal-title-group>
<issn pub-type="ppub">1687-9627</issn>
<issn pub-type="epub">1687-9635</issn>
<publisher>
<publisher-name>Hindawi Publishing Corporation</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">25140178</article-id>
<article-id pub-id-type="pmc">4124701</article-id>
<article-id pub-id-type="doi">10.1155/2014/281313</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Case Report</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Concomitant Factors Leading to an Atypical Osteonecrosis of the Jaw in a Patient with Multiple Myeloma</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Miranda-Rius</surname>
<given-names>Jaume</given-names>
</name>
<xref ref-type="aff" rid="I1">
<sup>1</sup>
</xref>
<xref ref-type="corresp" rid="cor1">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Brunet-Llobet</surname>
<given-names>Lluís</given-names>
</name>
<xref ref-type="aff" rid="I2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Lahor-Soler</surname>
<given-names>Eduard</given-names>
</name>
<xref ref-type="aff" rid="I1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Giménez-Rubio</surname>
<given-names>Josep Anton</given-names>
</name>
<xref ref-type="aff" rid="I3">
<sup>3</sup>
</xref>
</contrib>
</contrib-group>
<aff id="I1">
<sup>1</sup>
Departament d'Odontostomatologia, Facultat d'Odontologia, Universitat de Barcelona, L'Hospitalet de Llobregat, 08907 Barcelona, Spain</aff>
<aff id="I2">
<sup>2</sup>
Servei d'Odontologia, Hospital Universitari Sant Joan de Déu, Universitat de Barcelona, Esplugues de Llobregat, 08950 Barcelona, Spain</aff>
<aff id="I3">
<sup>3</sup>
Servei de Cirurgia Oral i Maxil
<italic>·</italic>
lofacial, Hospital Universitari Mútua de Terrassa, Universitat de Barcelona, Terrassa, 08221 Barcelona, Spain</aff>
<author-notes>
<corresp id="cor1">*Jaume Miranda-Rius:
<email>jmiranda-rius@ub.edu</email>
</corresp>
<fn fn-type="other">
<p>Academic Editor: Werner Rabitsch</p>
</fn>
</author-notes>
<pub-date pub-type="ppub">
<year>2014</year>
</pub-date>
<pub-date pub-type="epub">
<day>16</day>
<month>7</month>
<year>2014</year>
</pub-date>
<volume>2014</volume>
<elocation-id>281313</elocation-id>
<history>
<date date-type="received">
<day>28</day>
<month>4</month>
<year>2014</year>
</date>
<date date-type="accepted">
<day>19</day>
<month>6</month>
<year>2014</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2014 Jaume Miranda-Rius et al.</copyright-statement>
<copyright-year>2014</copyright-year>
<license xlink:href="https://creativecommons.org/licenses/by/3.0/">
<license-p>This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<abstract>
<p>Osteonecrosis of the jaw (ONJ) is a site specific osseous pathology, characterized by chronic exposed bone in the mouth, which needs to be reinforced periodically within the medical literature. ONJ is a clinical entity with many possible aetiologies and its pathogenesis is not well understood. The risk factors for ONJ include bisphosphonates treatments, head and neck radiotherapy, dental procedures involving bone surgery, and trauma. Management of ONJ has centred on efforts to eliminate or reduce severity of symptoms, to slow or prevent the progression of disease, and to eradicate diseased bone. This case describes a rare case of ONJ in a 64-year-old Caucasian male diagnosed with multiple myeloma stage III. The lesion was related to a traumatic injury during mastication. Eighteen months ago in the same area the molar 37 was extracted, achieving a complete satisfactory healing, when only 2 doses of zoledronic acid had been administered.
<italic>Actinomyces</italic>
bacterial aggregates were also identified in the microscopic analysis. The management of this osteonecrotic lesion included antibiotic treatment and chlorhexidine topical gel administration. The evolution was monitored every two weeks until patient's death. The authors provide a discussion of the etiology, pathogenesis, diagnosis, and management. This case report may shed light on the controversies about concomitant factors and mechanisms inducing ONJ.</p>
</abstract>
</article-meta>
</front>
<floats-group>
<fig id="fig1" orientation="portrait" position="float">
<label>Figure 1</label>
<caption>
<p>(a) Clinical image. Chronic suppurated apical periodontitis of tooth 37. Notice the fistula in the buccal area of this molar. (b) Radiological image. Notice the periapical radiolucent lesion in tooth 37.</p>
</caption>
<graphic xlink:href="CRIM2014-281313.001"></graphic>
</fig>
<fig id="fig2" orientation="portrait" position="float">
<label>Figure 2</label>
<caption>
<p>(a) Panoramic radiograph. Notice the correct healing of the socket after 6 months of the molar 37 extraction. (b) Periapical radiograph. Observe the satisfactory bone density in the socket after 6 months of extraction.</p>
</caption>
<graphic xlink:href="CRIM2014-281313.002"></graphic>
</fig>
<fig id="fig3" orientation="portrait" position="float">
<label>Figure 3</label>
<caption>
<p>Clinical image. Progression of the lesion. (a) Notice the incipient mucositis and light tumefaction on the affected area. (b) Six weeks later, notice the bone exposure and how the lesion is expanding in mesial direction. ((c) and (d)) Eight weeks later, notice the increase of bone exposure and a characteristic sinus tract with its active exudation.</p>
</caption>
<graphic xlink:href="CRIM2014-281313.003"></graphic>
</fig>
<fig id="fig4" orientation="portrait" position="float">
<label>Figure 4</label>
<caption>
<p>(a) Panoramic radiograph. Notice in the affected area a high bone density image. (b) CT image. Notice a lingual thin fissure line in the affected area.</p>
</caption>
<graphic xlink:href="CRIM2014-281313.004"></graphic>
</fig>
<fig id="fig5" orientation="portrait" position="float">
<label>Figure 5</label>
<caption>
<p>Microscopic appearance. (a) Necrotic bone fragment with acute inflammatory reaction with polymorphonuclear. H&E. Original magnification 20x. (b) Notice also the large bacterial aggregate consistent with
<italic> Actinomyces</italic>
. H&E. Original magnification 20x.</p>
</caption>
<graphic xlink:href="CRIM2014-281313.005"></graphic>
</fig>
<table-wrap id="tab1" orientation="portrait" position="float">
<label>Table 1</label>
<caption>
<p>International Staging System (ISS) for multiple myeloma.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" rowspan="1" colspan="1">Stage</th>
<th align="left" rowspan="1" colspan="1">Criteria</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="1" colspan="1">I</td>
<td align="left" rowspan="1" colspan="1">Serum
<italic>β</italic>
<sub>2</sub>
microglobulin < 3.5 mg/L and serum albumin ≥ 3.5 g/dL</td>
</tr>
<tr>
<td align="center" colspan="2" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">II</td>
<td align="left" rowspan="1" colspan="1">Serum
<italic>β</italic>
<sub>2</sub>
microglobulin < 3.5 mg/L but serum albumin < 3.5 g/dL or serum
<italic>β</italic>
<sub>2</sub>
microglobulin 3.5 to < 5.5 mg/L irrespective of the serum albumin level</td>
</tr>
<tr>
<td align="center" colspan="2" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">III</td>
<td align="left" rowspan="1" colspan="1">Serum
<italic>β</italic>
<sub>2</sub>
microglobulin ≥ 5.5 mg/L</td>
</tr>
</tbody>
</table>
</table-wrap>
<table-wrap id="tab2" orientation="portrait" position="float">
<label>Table 2</label>
<caption>
<p>ONM staging and treatment strategies—American Association of Oral and Maxillofacial Surgeons 2009.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" rowspan="1" colspan="1">ONJ stage</th>
<th align="left" rowspan="1" colspan="1">Description</th>
<th align="left" rowspan="1" colspan="1">Treatment strategies</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="1" colspan="1">At risk category</td>
<td align="left" rowspan="1" colspan="1">No apparent necrotic bone in patients who have been treated with either oral or IV bisphosphonates</td>
<td align="left" rowspan="1" colspan="1">No treatment indicated
<break></break>
Patient education</td>
</tr>
<tr>
<td align="center" colspan="3" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Stage 0</td>
<td align="left" rowspan="1" colspan="1">No clinical evidence of necrotic bone, but nonspecific clinical findings and symptoms</td>
<td align="left" rowspan="1" colspan="1">Systemic management, including use of pain medication and antibiotics</td>
</tr>
<tr>
<td align="center" colspan="3" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Stage 1</td>
<td align="left" rowspan="1" colspan="1">Exposed and necrotic bone in asymptomatic patients without evidence of infection</td>
<td align="left" rowspan="1" colspan="1">Antibacterial mouth rinse
<break></break>
Clinical follow-up on quarterly basis
<break></break>
Patient education and review of indications for continued bisphosphonate therapy</td>
</tr>
<tr>
<td align="center" colspan="3" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Stage 2</td>
<td align="left" rowspan="1" colspan="1">Exposed and necrotic bone associated with infection as evidenced by pain and erythema in region of exposed bone with or without purulent drainage</td>
<td align="left" rowspan="1" colspan="1">Symptomatic treatment with oral antibiotics
<break></break>
Oral antibacterial mouth rinse
<break></break>
Pain control
<break></break>
Superficial debridement to relieve soft tissue irritation</td>
</tr>
<tr>
<td align="center" colspan="3" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Stage 3</td>
<td align="left" rowspan="1" colspan="1">Exposed and necrotic bone in patients with pain, infection, and one or more of the following: A—exposed and necrotic bone extending beyond the region of alveolar bone, (i.e., inferior border and ramus in the mandible or maxillary sinus and zygoma in the maxilla) resulting in pathologic fracture, B—extraoral fistula and oral antral/oral nasal communication, and C—osteolysis extending to the inferior border of the mandible or the sinus floor</td>
<td align="left" rowspan="1" colspan="1">Antibacterial mouth rinse
<break></break>
Antibiotic therapy and pain control
<break></break>
Surgical debridement/resection for longer term palliation of infection and pain.</td>
</tr>
</tbody>
</table>
</table-wrap>
<table-wrap id="tab3" orientation="portrait" position="float">
<label>Table 3</label>
<caption>
<p>Anti-infective pharmacologic treatments∗.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" rowspan="1" colspan="1">Treatment</th>
<th align="left" rowspan="1" colspan="1">Dose and schedule</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="1" colspan="1">Antibacterials</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1"> Penicillin VK</td>
<td align="left" rowspan="1" colspan="1">500 mg every 6 to 8 hours for 7 to 10 days and then every 12 hours for maintenance</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1"> Amoxicillin</td>
<td align="left" rowspan="1" colspan="1">500 mg every 8 hours for 7 to 10 days and then every 12 hours for maintenance</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Patients with penicillin allergy</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1"> Clindamycin</td>
<td align="left" rowspan="1" colspan="1">150 to 300 mg every 6 hours</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1"> Vibramycin</td>
<td align="left" rowspan="1" colspan="1">100 mg every 24 hours</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1"> Erythromycin ethylsuccinate</td>
<td align="left" rowspan="1" colspan="1">400 mg every 8 hours</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1"> Azithromycin</td>
<td align="left" rowspan="1" colspan="1">500 mg PO × 1 on day 1; 250 mg oral every 6 hours on days 2 to 5</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Antifungals
<sup></sup>
(when required)</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1"> Nystatin oral suspension</td>
<td align="left" rowspan="1" colspan="1">5 to 15 mL every 6 hours or 100.000 IU/mL</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1"> Clotrimazole</td>
<td align="left" rowspan="1" colspan="1">10 mg every 8 hours and every 5 hours on days 7 to 10</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1"> Fluconazole</td>
<td align="left" rowspan="1" colspan="1">200 mg initially and then 100 mg every 24 hours</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Antivirals
<sup></sup>
</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1"> Acyclovir</td>
<td align="left" rowspan="1" colspan="1">400 mg every 12 hours</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1"> Valacyclovir hydrochloride</td>
<td align="left" rowspan="1" colspan="1">500 mg to 2 g every 12 hours</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>
<sup></sup>
Other potential systemic antifungals include itraconazole or ketoconazole.</p>
</fn>
<fn>
<p>
<sup></sup>
Role of antivirals in the treatment of osteonecrosis of the jaw has not yet been established.</p>
</fn>
<fn>
<p>∗Novartis (Basel, Switzerland), data on file.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</floats-group>
</pmc>
<affiliations>
<list>
<country>
<li>Espagne</li>
</country>
<region>
<li>Catalogne</li>
</region>
<settlement>
<li>Barcelone</li>
</settlement>
<orgName>
<li>Université de Barcelone</li>
</orgName>
</list>
<tree>
<country name="Espagne">
<region name="Catalogne">
<name sortKey="Miranda Rius, Jaume" sort="Miranda Rius, Jaume" uniqKey="Miranda Rius J" first="Jaume" last="Miranda-Rius">Jaume Miranda-Rius</name>
</region>
<name sortKey="Brunet Llobet, Lluis" sort="Brunet Llobet, Lluis" uniqKey="Brunet Llobet L" first="Lluís" last="Brunet-Llobet">Lluís Brunet-Llobet</name>
<name sortKey="Gimenez Rubio, Josep Anton" sort="Gimenez Rubio, Josep Anton" uniqKey="Gimenez Rubio J" first="Josep Anton" last="Giménez-Rubio">Josep Anton Giménez-Rubio</name>
<name sortKey="Lahor Soler, Eduard" sort="Lahor Soler, Eduard" uniqKey="Lahor Soler E" first="Eduard" last="Lahor-Soler">Eduard Lahor-Soler</name>
</country>
</tree>
</affiliations>
</record>

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   |texte=   Concomitant Factors Leading to an Atypical Osteonecrosis of the Jaw in a Patient with Multiple Myeloma
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