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Brown Tumors of the Jaws: A Retrospective Study
Objectives: (1) Describe the clinical spectrum, imaging features, management, and outcome of brown tumors (BT) of the jaws. (2) Determine via a literature review the facts and controversies around the characteristics and management of this lesion. Materials and methods: Our study was approved by the...
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Published in: | Clinical medicine insights. Endocrinology and diabetes 2023-01, Vol.16, p.11795514231210143-11795514231210143 |
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creator | Fedhila, Maya Belkacem Chebil, Raouaa Marmouch, Hela Terchalla, Sabrine Ayachi, Samia Oueslati, Yassine Oualha, Lamia Douki, Nabiha Khochtali, Habib |
description | Objectives:
(1) Describe the clinical spectrum, imaging features, management, and outcome of brown tumors (BT) of the jaws. (2) Determine via a literature review the facts and controversies around the characteristics and management of this lesion.
Materials and methods:
Our study was approved by the institutional committee of Sahloul University Hospital in accordance with the ethical standards of the Declaration of Helsinki. Sixteen patients with BT in the context of a primary, secondary, and tertiary hyperparathyroidism were treated and followed up during their recovery.
Results:
This study reports 16 patients with a mean age of 48 years old. Brown tumor lesions were associated with primary hyperparathyroidism in 6 cases (38%), secondary hyperparathyroidism to chronic kidney failure in 5 cases (31%), and tertiary hyperparathyroidism in the context of a long lasting CRI in 5 cases. Their location was maxillary in 7 cases, mandibular in 5 cases, and bimaxillary in 4 cases. The treatment consisted of parathyroidectomy in 13 patients, maxillary resection in 3 cases, and vitamin D treatment in 2 cases. Favorable outcomes, characterized by tumor regression, were reported in 9 cases, whereas unfavorable evolution was observed among 7 patients.
Conclusion:
Parathyroidectomy is the gold standard treatment for primary hyperparathyroidism. It resulted in a total regression in all our cases. Regarding secondary hyperparathyroidism, blood screening and chronic renal insufficiency follow-up are critically valuable to detect this condition at an early stage, hence increasing the success rate of brown tumor regression. Our secondary and tertiary hyperparathyroidism results were miscellaneous; although it is important to emphasize the importance of the chronic renal insufficiency management to ensure a success.
Clinical relevance:
Brown tumors should be included in the differential diagnosis of giant cell lesions. Parathyroidectomy is usually sufficient to induce the total regression of the lesion in primary hyperparathyroidism cases. A more delicate approach is needed regarding secondary hyperparathyroidism. Meticulous control of chronic renal insufficiency is mandatory in addition to parathyroidectomy. |
doi_str_mv | 10.1177/11795514231210143 |
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(1) Describe the clinical spectrum, imaging features, management, and outcome of brown tumors (BT) of the jaws. (2) Determine via a literature review the facts and controversies around the characteristics and management of this lesion.
Materials and methods:
Our study was approved by the institutional committee of Sahloul University Hospital in accordance with the ethical standards of the Declaration of Helsinki. Sixteen patients with BT in the context of a primary, secondary, and tertiary hyperparathyroidism were treated and followed up during their recovery.
Results:
This study reports 16 patients with a mean age of 48 years old. Brown tumor lesions were associated with primary hyperparathyroidism in 6 cases (38%), secondary hyperparathyroidism to chronic kidney failure in 5 cases (31%), and tertiary hyperparathyroidism in the context of a long lasting CRI in 5 cases. Their location was maxillary in 7 cases, mandibular in 5 cases, and bimaxillary in 4 cases. The treatment consisted of parathyroidectomy in 13 patients, maxillary resection in 3 cases, and vitamin D treatment in 2 cases. Favorable outcomes, characterized by tumor regression, were reported in 9 cases, whereas unfavorable evolution was observed among 7 patients.
Conclusion:
Parathyroidectomy is the gold standard treatment for primary hyperparathyroidism. It resulted in a total regression in all our cases. Regarding secondary hyperparathyroidism, blood screening and chronic renal insufficiency follow-up are critically valuable to detect this condition at an early stage, hence increasing the success rate of brown tumor regression. Our secondary and tertiary hyperparathyroidism results were miscellaneous; although it is important to emphasize the importance of the chronic renal insufficiency management to ensure a success.
Clinical relevance:
Brown tumors should be included in the differential diagnosis of giant cell lesions. Parathyroidectomy is usually sufficient to induce the total regression of the lesion in primary hyperparathyroidism cases. A more delicate approach is needed regarding secondary hyperparathyroidism. Meticulous control of chronic renal insufficiency is mandatory in addition to parathyroidectomy.</description><identifier>ISSN: 1179-5514</identifier><identifier>EISSN: 1179-5514</identifier><identifier>DOI: 10.1177/11795514231210143</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Bone cancer ; Endocrine disorders ; Original Research ; Tumors</subject><ispartof>Clinical medicine insights. Endocrinology and diabetes, 2023-01, Vol.16, p.11795514231210143-11795514231210143</ispartof><rights>The Author(s) 2023</rights><rights>The Author(s) 2023. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2023 2023 SAGE Publications Ltd unless otherwise noted. Manuscript content on this site is licensed under Creative Commons Licenses</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c510t-5ff314366c43b475ba53e85546b3d558586170c2d73e8ea04cc70f539de96f113</citedby><cites>FETCH-LOGICAL-c510t-5ff314366c43b475ba53e85546b3d558586170c2d73e8ea04cc70f539de96f113</cites><orcidid>0000-0002-1832-3487 ; 0000-0002-5100-9908</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10629299/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2920162701?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,21966,25753,27853,27924,27925,37012,37013,44590,44945,45333,53791,53793</link.rule.ids></links><search><creatorcontrib>Fedhila, Maya</creatorcontrib><creatorcontrib>Belkacem Chebil, Raouaa</creatorcontrib><creatorcontrib>Marmouch, Hela</creatorcontrib><creatorcontrib>Terchalla, Sabrine</creatorcontrib><creatorcontrib>Ayachi, Samia</creatorcontrib><creatorcontrib>Oueslati, Yassine</creatorcontrib><creatorcontrib>Oualha, Lamia</creatorcontrib><creatorcontrib>Douki, Nabiha</creatorcontrib><creatorcontrib>Khochtali, Habib</creatorcontrib><title>Brown Tumors of the Jaws: A Retrospective Study</title><title>Clinical medicine insights. Endocrinology and diabetes</title><description>Objectives:
(1) Describe the clinical spectrum, imaging features, management, and outcome of brown tumors (BT) of the jaws. (2) Determine via a literature review the facts and controversies around the characteristics and management of this lesion.
Materials and methods:
Our study was approved by the institutional committee of Sahloul University Hospital in accordance with the ethical standards of the Declaration of Helsinki. Sixteen patients with BT in the context of a primary, secondary, and tertiary hyperparathyroidism were treated and followed up during their recovery.
Results:
This study reports 16 patients with a mean age of 48 years old. Brown tumor lesions were associated with primary hyperparathyroidism in 6 cases (38%), secondary hyperparathyroidism to chronic kidney failure in 5 cases (31%), and tertiary hyperparathyroidism in the context of a long lasting CRI in 5 cases. Their location was maxillary in 7 cases, mandibular in 5 cases, and bimaxillary in 4 cases. The treatment consisted of parathyroidectomy in 13 patients, maxillary resection in 3 cases, and vitamin D treatment in 2 cases. Favorable outcomes, characterized by tumor regression, were reported in 9 cases, whereas unfavorable evolution was observed among 7 patients.
Conclusion:
Parathyroidectomy is the gold standard treatment for primary hyperparathyroidism. It resulted in a total regression in all our cases. Regarding secondary hyperparathyroidism, blood screening and chronic renal insufficiency follow-up are critically valuable to detect this condition at an early stage, hence increasing the success rate of brown tumor regression. Our secondary and tertiary hyperparathyroidism results were miscellaneous; although it is important to emphasize the importance of the chronic renal insufficiency management to ensure a success.
Clinical relevance:
Brown tumors should be included in the differential diagnosis of giant cell lesions. Parathyroidectomy is usually sufficient to induce the total regression of the lesion in primary hyperparathyroidism cases. A more delicate approach is needed regarding secondary hyperparathyroidism. Meticulous control of chronic renal insufficiency is mandatory in addition to parathyroidectomy.</description><subject>Bone cancer</subject><subject>Endocrine disorders</subject><subject>Original Research</subject><subject>Tumors</subject><issn>1179-5514</issn><issn>1179-5514</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kUtLAzEUhQdRsKg_wN2AGzfVPGcSN6Lik4LgYx0ymZt2ynRSk5mW_nsztvjELJJwcs-Xw71JcojRCcZ5fho3yTlmhGKCEWZ0Kxn02rAXt7_dd5ODEKYoLiYp5XSQnF56t2zSl27mfEidTdsJpA96Gc7Si_QJWu_CHExbLSB9brtytZ_sWF0HONice8nrzfXL1d1w9Hh7f3UxGhqOUTvk1tKYI8sMowXLeaE5BcE5ywpaci64yHCODCnzKINGzJgcWU5lCTKzGNO95H7NLZ2eqrmvZtqvlNOV-hCcHyvt28rUoGQmC0OpYFJbJiyVgmHgiMQgYAF61vmaNe-KGZQGmtbr-gf050tTTdTYLRRGGZFEykg43hC8e-sgtGpWBQN1rRtwXVBECIEoZaT_7OhX6dR1vom9UpGFcEZy1FfhdZWJDQ4e7GcajFQ_U_VnptFzsvYEPYYv6v-Gd6PInWQ</recordid><startdate>20230101</startdate><enddate>20230101</enddate><creator>Fedhila, Maya</creator><creator>Belkacem Chebil, Raouaa</creator><creator>Marmouch, Hela</creator><creator>Terchalla, Sabrine</creator><creator>Ayachi, Samia</creator><creator>Oueslati, Yassine</creator><creator>Oualha, Lamia</creator><creator>Douki, Nabiha</creator><creator>Khochtali, Habib</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><general>SAGE Publishing</general><scope>AFRWT</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AYAGU</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-1832-3487</orcidid><orcidid>https://orcid.org/0000-0002-5100-9908</orcidid></search><sort><creationdate>20230101</creationdate><title>Brown Tumors of the Jaws: A Retrospective Study</title><author>Fedhila, Maya ; Belkacem Chebil, Raouaa ; Marmouch, Hela ; Terchalla, Sabrine ; Ayachi, Samia ; Oueslati, Yassine ; Oualha, Lamia ; Douki, Nabiha ; Khochtali, Habib</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c510t-5ff314366c43b475ba53e85546b3d558586170c2d73e8ea04cc70f539de96f113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Bone cancer</topic><topic>Endocrine disorders</topic><topic>Original Research</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fedhila, Maya</creatorcontrib><creatorcontrib>Belkacem Chebil, Raouaa</creatorcontrib><creatorcontrib>Marmouch, Hela</creatorcontrib><creatorcontrib>Terchalla, Sabrine</creatorcontrib><creatorcontrib>Ayachi, Samia</creatorcontrib><creatorcontrib>Oueslati, Yassine</creatorcontrib><creatorcontrib>Oualha, Lamia</creatorcontrib><creatorcontrib>Douki, Nabiha</creatorcontrib><creatorcontrib>Khochtali, Habib</creatorcontrib><collection>Sage Journals GOLD Open Access 2024</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>Australia & New Zealand Database</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Databases</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Clinical medicine insights. Endocrinology and diabetes</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fedhila, Maya</au><au>Belkacem Chebil, Raouaa</au><au>Marmouch, Hela</au><au>Terchalla, Sabrine</au><au>Ayachi, Samia</au><au>Oueslati, Yassine</au><au>Oualha, Lamia</au><au>Douki, Nabiha</au><au>Khochtali, Habib</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Brown Tumors of the Jaws: A Retrospective Study</atitle><jtitle>Clinical medicine insights. Endocrinology and diabetes</jtitle><date>2023-01-01</date><risdate>2023</risdate><volume>16</volume><spage>11795514231210143</spage><epage>11795514231210143</epage><pages>11795514231210143-11795514231210143</pages><issn>1179-5514</issn><eissn>1179-5514</eissn><abstract>Objectives:
(1) Describe the clinical spectrum, imaging features, management, and outcome of brown tumors (BT) of the jaws. (2) Determine via a literature review the facts and controversies around the characteristics and management of this lesion.
Materials and methods:
Our study was approved by the institutional committee of Sahloul University Hospital in accordance with the ethical standards of the Declaration of Helsinki. Sixteen patients with BT in the context of a primary, secondary, and tertiary hyperparathyroidism were treated and followed up during their recovery.
Results:
This study reports 16 patients with a mean age of 48 years old. Brown tumor lesions were associated with primary hyperparathyroidism in 6 cases (38%), secondary hyperparathyroidism to chronic kidney failure in 5 cases (31%), and tertiary hyperparathyroidism in the context of a long lasting CRI in 5 cases. Their location was maxillary in 7 cases, mandibular in 5 cases, and bimaxillary in 4 cases. The treatment consisted of parathyroidectomy in 13 patients, maxillary resection in 3 cases, and vitamin D treatment in 2 cases. Favorable outcomes, characterized by tumor regression, were reported in 9 cases, whereas unfavorable evolution was observed among 7 patients.
Conclusion:
Parathyroidectomy is the gold standard treatment for primary hyperparathyroidism. It resulted in a total regression in all our cases. Regarding secondary hyperparathyroidism, blood screening and chronic renal insufficiency follow-up are critically valuable to detect this condition at an early stage, hence increasing the success rate of brown tumor regression. Our secondary and tertiary hyperparathyroidism results were miscellaneous; although it is important to emphasize the importance of the chronic renal insufficiency management to ensure a success.
Clinical relevance:
Brown tumors should be included in the differential diagnosis of giant cell lesions. Parathyroidectomy is usually sufficient to induce the total regression of the lesion in primary hyperparathyroidism cases. A more delicate approach is needed regarding secondary hyperparathyroidism. Meticulous control of chronic renal insufficiency is mandatory in addition to parathyroidectomy.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><doi>10.1177/11795514231210143</doi><orcidid>https://orcid.org/0000-0002-1832-3487</orcidid><orcidid>https://orcid.org/0000-0002-5100-9908</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bone cancer Endocrine disorders Original Research Tumors |
title | Brown Tumors of the Jaws: A Retrospective Study |
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