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Nivolumab-induced oral and cutaneous bullous pemphigoid: A case report
Introduction: Nivolumab-induced oral and cutaneous bullous pemphigoid have been rarely reported in the literature. Observations: A 64-year-old male patient was treated with nivolumab for melanoma. He presented with oral lesions in the palatal and gingival mucosal lesions. Nine months after the initi...
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Published in: | Journal of oral medicine and oral surgery 2019, Vol.25 (2), p.17 |
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description | Introduction:
Nivolumab-induced oral and cutaneous bullous pemphigoid have been rarely reported in the literature.
Observations:
A 64-year-old male patient was treated with nivolumab for melanoma. He presented with oral lesions in the palatal and gingival mucosal lesions. Nine months after the initiation of nivolumab therapy, a cutaneous bullous pemphigoid was found on his right forearm. The level of anti-BPAG2 (or anti-BP 180) was positive with a rate of 83 AU/mL, thereby confirming the diagnosis of bullous pemphigoid. His oral mucosa, first in the posterolateral area of the palate and then in the gingiva, was affected 3 months later. Histological examination revealed a subepidermal bulla with few eosinophils.
Comments:
Nivolumab is a novel monoclonal human antibody used to potentiate T cell responses, particularly anti-tumor responses. The first diagnosis considered was lichen planus, and it has been excluded from this study based on histological results. Right from lesion onset after treatment initiation, nivolumab was strongly suspected to cause these mucocutaneous lesions. To investigate the causes and effects of nivolumab-induced oral and cutaneous bullous pemphigoid, it would be necessary to record the regression of these lesions at the end of treatment; however, this is not possible due to ethical reasons. The treatment of lesions primarily involves corticosteroid usage; however, rituximab is also used.
Conclusion:
Oral surgeons must consider the oral side effects of novel targeted therapies, including those of immunological checkpoint inhibitors. |
doi_str_mv | 10.1051/mbcb/2019001 |
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Nivolumab-induced oral and cutaneous bullous pemphigoid have been rarely reported in the literature.
Observations:
A 64-year-old male patient was treated with nivolumab for melanoma. He presented with oral lesions in the palatal and gingival mucosal lesions. Nine months after the initiation of nivolumab therapy, a cutaneous bullous pemphigoid was found on his right forearm. The level of anti-BPAG2 (or anti-BP 180) was positive with a rate of 83 AU/mL, thereby confirming the diagnosis of bullous pemphigoid. His oral mucosa, first in the posterolateral area of the palate and then in the gingiva, was affected 3 months later. Histological examination revealed a subepidermal bulla with few eosinophils.
Comments:
Nivolumab is a novel monoclonal human antibody used to potentiate T cell responses, particularly anti-tumor responses. The first diagnosis considered was lichen planus, and it has been excluded from this study based on histological results. Right from lesion onset after treatment initiation, nivolumab was strongly suspected to cause these mucocutaneous lesions. To investigate the causes and effects of nivolumab-induced oral and cutaneous bullous pemphigoid, it would be necessary to record the regression of these lesions at the end of treatment; however, this is not possible due to ethical reasons. The treatment of lesions primarily involves corticosteroid usage; however, rituximab is also used.
Conclusion:
Oral surgeons must consider the oral side effects of novel targeted therapies, including those of immunological checkpoint inhibitors.</description><identifier>ISSN: 2608-1326</identifier><identifier>EISSN: 2608-1326</identifier><identifier>DOI: 10.1051/mbcb/2019001</identifier><language>eng</language><publisher>Les Ulis: EDP Sciences</publisher><subject>bullous ; Bullous pemphigoid ; Case reports ; Corticosteroids ; Diagnosis ; Forearm ; Immunotherapy ; Leukocytes (eosinophilic) ; Lichen planus ; Lymphocytes T ; Melanoma ; Monoclonal antibodies ; mouth ; Mucosa ; nivolumab ; Palate ; pemphigoid ; Rituximab ; Targeted cancer therapy</subject><ispartof>Journal of oral medicine and oral surgery, 2019, Vol.25 (2), p.17</ispartof><rights>2019. This work is licensed under http://creativecommons.org/licenses/by/4.0 (the “License”). Notwithstanding the ProQuest Terms and conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2821-1ab2ac71aaef048c257dec3de065304edb949b2684453f182e896daf1df1ac873</citedby><cites>FETCH-LOGICAL-c2821-1ab2ac71aaef048c257dec3de065304edb949b2684453f182e896daf1df1ac873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2233084608?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,4024,25753,27923,27924,27925,37012,44590</link.rule.ids></links><search><creatorcontrib>Sturque, Julie</creatorcontrib><creatorcontrib>Boralevi, Franck</creatorcontrib><creatorcontrib>Fricain, Jean-Christophe</creatorcontrib><title>Nivolumab-induced oral and cutaneous bullous pemphigoid: A case report</title><title>Journal of oral medicine and oral surgery</title><description>Introduction:
Nivolumab-induced oral and cutaneous bullous pemphigoid have been rarely reported in the literature.
Observations:
A 64-year-old male patient was treated with nivolumab for melanoma. He presented with oral lesions in the palatal and gingival mucosal lesions. Nine months after the initiation of nivolumab therapy, a cutaneous bullous pemphigoid was found on his right forearm. The level of anti-BPAG2 (or anti-BP 180) was positive with a rate of 83 AU/mL, thereby confirming the diagnosis of bullous pemphigoid. His oral mucosa, first in the posterolateral area of the palate and then in the gingiva, was affected 3 months later. Histological examination revealed a subepidermal bulla with few eosinophils.
Comments:
Nivolumab is a novel monoclonal human antibody used to potentiate T cell responses, particularly anti-tumor responses. The first diagnosis considered was lichen planus, and it has been excluded from this study based on histological results. Right from lesion onset after treatment initiation, nivolumab was strongly suspected to cause these mucocutaneous lesions. To investigate the causes and effects of nivolumab-induced oral and cutaneous bullous pemphigoid, it would be necessary to record the regression of these lesions at the end of treatment; however, this is not possible due to ethical reasons. The treatment of lesions primarily involves corticosteroid usage; however, rituximab is also used.
Conclusion:
Oral surgeons must consider the oral side effects of novel targeted therapies, including those of immunological checkpoint inhibitors.</description><subject>bullous</subject><subject>Bullous pemphigoid</subject><subject>Case reports</subject><subject>Corticosteroids</subject><subject>Diagnosis</subject><subject>Forearm</subject><subject>Immunotherapy</subject><subject>Leukocytes (eosinophilic)</subject><subject>Lichen planus</subject><subject>Lymphocytes T</subject><subject>Melanoma</subject><subject>Monoclonal antibodies</subject><subject>mouth</subject><subject>Mucosa</subject><subject>nivolumab</subject><subject>Palate</subject><subject>pemphigoid</subject><subject>Rituximab</subject><subject>Targeted cancer therapy</subject><issn>2608-1326</issn><issn>2608-1326</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpNkEtLw0AUhQdRsNTu_AEBt8bOK5MZd6VYLRTd6Hq480hNSTJxJhH896ZWxNU5XA7nHj6Ergm-I7ggy9ZYs6SYKIzJGZpRgWVOGBXn__wlWqR0wBhTzKUqxAxtnuvP0IwtmLzu3Gi9y0KEJoPOZXYcoPNhTJkZm-aovW_793ofanefrTILyWfR9yEOV-iigib5xa_O0dvm4XX9lO9eHrfr1S63VFKSEzAUbEkAfDUtsLQonbfMeSwKhrl3RnFlqJCcF6wiknqphIOKuIqAlSWbo-2p1wU46D7WLcQvHaDWP4cQ9xriUNvGa0EBKigcpcpw4EI5pywQ40rGy7JwU9fNqauP4WP0adCHMMZumq8pZQxLPmGbUrenlI0hpeirv68E6yN4fQSvf8GzbzJJdYk</recordid><startdate>2019</startdate><enddate>2019</enddate><creator>Sturque, Julie</creator><creator>Boralevi, Franck</creator><creator>Fricain, Jean-Christophe</creator><general>EDP Sciences</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope></search><sort><creationdate>2019</creationdate><title>Nivolumab-induced oral and cutaneous bullous pemphigoid: A case report</title><author>Sturque, Julie ; Boralevi, Franck ; Fricain, Jean-Christophe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2821-1ab2ac71aaef048c257dec3de065304edb949b2684453f182e896daf1df1ac873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>bullous</topic><topic>Bullous pemphigoid</topic><topic>Case reports</topic><topic>Corticosteroids</topic><topic>Diagnosis</topic><topic>Forearm</topic><topic>Immunotherapy</topic><topic>Leukocytes (eosinophilic)</topic><topic>Lichen planus</topic><topic>Lymphocytes T</topic><topic>Melanoma</topic><topic>Monoclonal antibodies</topic><topic>mouth</topic><topic>Mucosa</topic><topic>nivolumab</topic><topic>Palate</topic><topic>pemphigoid</topic><topic>Rituximab</topic><topic>Targeted cancer therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sturque, Julie</creatorcontrib><creatorcontrib>Boralevi, Franck</creatorcontrib><creatorcontrib>Fricain, Jean-Christophe</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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 Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</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>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of oral medicine and oral surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sturque, Julie</au><au>Boralevi, Franck</au><au>Fricain, Jean-Christophe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nivolumab-induced oral and cutaneous bullous pemphigoid: A case report</atitle><jtitle>Journal of oral medicine and oral surgery</jtitle><date>2019</date><risdate>2019</risdate><volume>25</volume><issue>2</issue><spage>17</spage><pages>17-</pages><issn>2608-1326</issn><eissn>2608-1326</eissn><abstract>Introduction:
Nivolumab-induced oral and cutaneous bullous pemphigoid have been rarely reported in the literature.
Observations:
A 64-year-old male patient was treated with nivolumab for melanoma. He presented with oral lesions in the palatal and gingival mucosal lesions. Nine months after the initiation of nivolumab therapy, a cutaneous bullous pemphigoid was found on his right forearm. The level of anti-BPAG2 (or anti-BP 180) was positive with a rate of 83 AU/mL, thereby confirming the diagnosis of bullous pemphigoid. His oral mucosa, first in the posterolateral area of the palate and then in the gingiva, was affected 3 months later. Histological examination revealed a subepidermal bulla with few eosinophils.
Comments:
Nivolumab is a novel monoclonal human antibody used to potentiate T cell responses, particularly anti-tumor responses. The first diagnosis considered was lichen planus, and it has been excluded from this study based on histological results. Right from lesion onset after treatment initiation, nivolumab was strongly suspected to cause these mucocutaneous lesions. To investigate the causes and effects of nivolumab-induced oral and cutaneous bullous pemphigoid, it would be necessary to record the regression of these lesions at the end of treatment; however, this is not possible due to ethical reasons. The treatment of lesions primarily involves corticosteroid usage; however, rituximab is also used.
Conclusion:
Oral surgeons must consider the oral side effects of novel targeted therapies, including those of immunological checkpoint inhibitors.</abstract><cop>Les Ulis</cop><pub>EDP Sciences</pub><doi>10.1051/mbcb/2019001</doi><oa>free_for_read</oa></addata></record> |
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subjects | bullous Bullous pemphigoid Case reports Corticosteroids Diagnosis Forearm Immunotherapy Leukocytes (eosinophilic) Lichen planus Lymphocytes T Melanoma Monoclonal antibodies mouth Mucosa nivolumab Palate pemphigoid Rituximab Targeted cancer therapy |
title | Nivolumab-induced oral and cutaneous bullous pemphigoid: A case report |
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