Orofacial granulomatosis: Clinical features and long-term outcome of therapy

Background Orofacial granulomatosis (OFG) is a chronic inflammatory disorder characterized by persistent or recurrent soft tissue enlargement, oral ulceration, and a variety of other orofacial features. There remain few detailed reports of the clinical features and long-term response to therapy of s...

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Veröffentlicht in:Journal of the American Academy of Dermatology 2010-04, Vol.62 (4), p.611-620
Hauptverfasser: Al Johani, Khalid A., BDS, MSc, Moles, David R., PhD, MSc (Hons), MIHPE, DDPH RCS (Eng), FHEA, Hodgson, Tim A., FDS, FDS (OM) RCS, MRCP (UK), FGDP (UK), Porter, Stephen R., PhD, MD, FDSRCS, FDSRCSE, Fedele, Stefano, DDS, PhD
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container_title Journal of the American Academy of Dermatology
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creator Al Johani, Khalid A., BDS, MSc
Moles, David R., PhD, MSc (Hons), MIHPE, DDPH RCS (Eng), FHEA
Hodgson, Tim A., FDS, FDS (OM) RCS, MRCP (UK), FGDP (UK)
Porter, Stephen R., PhD, MD, FDSRCS, FDSRCSE
Fedele, Stefano, DDS, PhD
description Background Orofacial granulomatosis (OFG) is a chronic inflammatory disorder characterized by persistent or recurrent soft tissue enlargement, oral ulceration, and a variety of other orofacial features. There remain few detailed reports of the clinical features and long-term response to therapy of substantial groups of patients with OFG. Objective The aim of this study was to determine retrospectively the clinical, hematologic, and histopathological features of a large case series of patients with OFG. In addition the long-term response to therapy was examined. Methods Clinically relevant data of 49 patients with OFG who attended a single oral medicine unit in the United Kingdom were retrospectively examined. The analyzed parameters included diagnostic features, clinical manifestations, and outcomes and adverse side effects of therapy. Results Labial swelling was the most common presenting clinical feature at diagnosis (75.5%), followed by intraoral mucosal features other than ulceration such as cobblestoning and gingival enlargement (73.5%). Mucosal ulceration was observed in 36.7% of patients whereas extraoral facial manifestations such as cutaneous erythema and swelling were present in 40.8% of patients. Of the 45 patients who required treatment, 24 (53.3%) were treated with topical corticosteroids/immunosuppressants only, whereas 21 (46.7%) received a combined therapy (topical plus systemic corticosteroids/immunosuppressants and/or intralesional corticosteroids). The long-term outcome analysis showed complete/partial resolution of tissue swelling and oral ulceration in 78.8% and 70% of patients, respectively. Limitations The main limitation of the current study was its retrospective design and methodology including differences in reporting clinical features and outcome. Conclusions OFG can show multiple facial and mucosal clinical features. Long-term treatment with topical and/or combined therapy is needed in the majority of patients. Response to therapy is highly variable even though in the long-term complete/partial disease resolution can be obtained in the majority of patients. Mucosal ulceration tends to be more recalcitrant than orofacial swelling. Adverse side effects of therapy are rare.
doi_str_mv 10.1016/j.jaad.2009.03.051
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There remain few detailed reports of the clinical features and long-term response to therapy of substantial groups of patients with OFG. Objective The aim of this study was to determine retrospectively the clinical, hematologic, and histopathological features of a large case series of patients with OFG. In addition the long-term response to therapy was examined. Methods Clinically relevant data of 49 patients with OFG who attended a single oral medicine unit in the United Kingdom were retrospectively examined. The analyzed parameters included diagnostic features, clinical manifestations, and outcomes and adverse side effects of therapy. Results Labial swelling was the most common presenting clinical feature at diagnosis (75.5%), followed by intraoral mucosal features other than ulceration such as cobblestoning and gingival enlargement (73.5%). Mucosal ulceration was observed in 36.7% of patients whereas extraoral facial manifestations such as cutaneous erythema and swelling were present in 40.8% of patients. Of the 45 patients who required treatment, 24 (53.3%) were treated with topical corticosteroids/immunosuppressants only, whereas 21 (46.7%) received a combined therapy (topical plus systemic corticosteroids/immunosuppressants and/or intralesional corticosteroids). The long-term outcome analysis showed complete/partial resolution of tissue swelling and oral ulceration in 78.8% and 70% of patients, respectively. Limitations The main limitation of the current study was its retrospective design and methodology including differences in reporting clinical features and outcome. Conclusions OFG can show multiple facial and mucosal clinical features. Long-term treatment with topical and/or combined therapy is needed in the majority of patients. Response to therapy is highly variable even though in the long-term complete/partial disease resolution can be obtained in the majority of patients. Mucosal ulceration tends to be more recalcitrant than orofacial swelling. Adverse side effects of therapy are rare.</description><identifier>ISSN: 0190-9622</identifier><identifier>EISSN: 1097-6787</identifier><identifier>DOI: 10.1016/j.jaad.2009.03.051</identifier><identifier>PMID: 20137827</identifier><identifier>CODEN: JAADDB</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Adolescent ; Adult ; Aged ; Biological and medical sciences ; Child ; clinical features ; Dermatology ; Female ; Granulomatosis, Orofacial - diagnosis ; Granulomatosis, Orofacial - drug therapy ; Humans ; long-term outcome ; Male ; Medical sciences ; Middle Aged ; orofacial granulomatosis ; Retrospective Studies ; Time Factors ; Treatment Outcome ; Young Adult</subject><ispartof>Journal of the American Academy of Dermatology, 2010-04, Vol.62 (4), p.611-620</ispartof><rights>American Academy of Dermatology, Inc.</rights><rights>2009 American Academy of Dermatology, Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright 2009 American Academy of Dermatology, Inc. 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All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c440t-a92e2dbe004cc5a36b0dacf4978f0e4e25d0355867981c8351c012f6c1f182853</citedby><cites>FETCH-LOGICAL-c440t-a92e2dbe004cc5a36b0dacf4978f0e4e25d0355867981c8351c012f6c1f182853</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jaad.2009.03.051$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=22575688$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20137827$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Al Johani, Khalid A., BDS, MSc</creatorcontrib><creatorcontrib>Moles, David R., PhD, MSc (Hons), MIHPE, DDPH RCS (Eng), FHEA</creatorcontrib><creatorcontrib>Hodgson, Tim A., FDS, FDS (OM) RCS, MRCP (UK), FGDP (UK)</creatorcontrib><creatorcontrib>Porter, Stephen R., PhD, MD, FDSRCS, FDSRCSE</creatorcontrib><creatorcontrib>Fedele, Stefano, DDS, PhD</creatorcontrib><title>Orofacial granulomatosis: Clinical features and long-term outcome of therapy</title><title>Journal of the American Academy of Dermatology</title><addtitle>J Am Acad Dermatol</addtitle><description>Background Orofacial granulomatosis (OFG) is a chronic inflammatory disorder characterized by persistent or recurrent soft tissue enlargement, oral ulceration, and a variety of other orofacial features. There remain few detailed reports of the clinical features and long-term response to therapy of substantial groups of patients with OFG. Objective The aim of this study was to determine retrospectively the clinical, hematologic, and histopathological features of a large case series of patients with OFG. In addition the long-term response to therapy was examined. Methods Clinically relevant data of 49 patients with OFG who attended a single oral medicine unit in the United Kingdom were retrospectively examined. The analyzed parameters included diagnostic features, clinical manifestations, and outcomes and adverse side effects of therapy. Results Labial swelling was the most common presenting clinical feature at diagnosis (75.5%), followed by intraoral mucosal features other than ulceration such as cobblestoning and gingival enlargement (73.5%). Mucosal ulceration was observed in 36.7% of patients whereas extraoral facial manifestations such as cutaneous erythema and swelling were present in 40.8% of patients. Of the 45 patients who required treatment, 24 (53.3%) were treated with topical corticosteroids/immunosuppressants only, whereas 21 (46.7%) received a combined therapy (topical plus systemic corticosteroids/immunosuppressants and/or intralesional corticosteroids). The long-term outcome analysis showed complete/partial resolution of tissue swelling and oral ulceration in 78.8% and 70% of patients, respectively. Limitations The main limitation of the current study was its retrospective design and methodology including differences in reporting clinical features and outcome. Conclusions OFG can show multiple facial and mucosal clinical features. Long-term treatment with topical and/or combined therapy is needed in the majority of patients. Response to therapy is highly variable even though in the long-term complete/partial disease resolution can be obtained in the majority of patients. Mucosal ulceration tends to be more recalcitrant than orofacial swelling. Adverse side effects of therapy are rare.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>clinical features</subject><subject>Dermatology</subject><subject>Female</subject><subject>Granulomatosis, Orofacial - diagnosis</subject><subject>Granulomatosis, Orofacial - drug therapy</subject><subject>Humans</subject><subject>long-term outcome</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>orofacial granulomatosis</subject><subject>Retrospective Studies</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>0190-9622</issn><issn>1097-6787</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUGL1DAUx4O4uOOuX8CD9CKeWl-StklEBBlcFQb2sOs5ZNKXNbVtxqQV5tubMuMKHjzl8H7_x8vvT8hLChUF2r7tq96YrmIAqgJeQUOfkA0FJcpWSPGUbIAqKFXL2CV5nlIPGay5eEYuGVAuJBMbsruNwRnrzVA8RDMtQxjNHJJP74rt4Cdv88ChmZeIqTBTVwxheihnjGMRltmGEYvgivk7RnM4XpMLZ4aEL87vFfl28-l--6Xc3X7-uv24K21dw1waxZB1ewSorW0Mb_fQGetqJaQDrJE1HfCmka1QklrJG2qBMtda6qhksuFX5M1p7yGGnwumWY8-WRwGM2FYkhY8_04oLjLJTqSNIaWITh-iH008agp6lah7vUrUq0QNXGeJOfTqvH7Zj9g9Rv5Yy8DrM2BSFuSyOOvTX441ommlzNz7E4dZxi-PUSfrcbLY-Yh21l3w_7_jwz9xe67kBx4x9WGJU9asqU5Mg75b617bBgUgQCn-G2htpCQ</recordid><startdate>20100401</startdate><enddate>20100401</enddate><creator>Al Johani, Khalid A., BDS, MSc</creator><creator>Moles, David R., PhD, MSc (Hons), MIHPE, DDPH RCS (Eng), FHEA</creator><creator>Hodgson, Tim A., FDS, FDS (OM) RCS, MRCP (UK), FGDP (UK)</creator><creator>Porter, Stephen R., PhD, MD, FDSRCS, FDSRCSE</creator><creator>Fedele, Stefano, DDS, PhD</creator><general>Mosby, Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20100401</creationdate><title>Orofacial granulomatosis: Clinical features and long-term outcome of therapy</title><author>Al Johani, Khalid A., BDS, MSc ; Moles, David R., PhD, MSc (Hons), MIHPE, DDPH RCS (Eng), FHEA ; Hodgson, Tim A., FDS, FDS (OM) RCS, MRCP (UK), FGDP (UK) ; Porter, Stephen R., PhD, MD, FDSRCS, FDSRCSE ; Fedele, Stefano, DDS, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-a92e2dbe004cc5a36b0dacf4978f0e4e25d0355867981c8351c012f6c1f182853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>clinical features</topic><topic>Dermatology</topic><topic>Female</topic><topic>Granulomatosis, Orofacial - diagnosis</topic><topic>Granulomatosis, Orofacial - drug therapy</topic><topic>Humans</topic><topic>long-term outcome</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>orofacial granulomatosis</topic><topic>Retrospective Studies</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Al Johani, Khalid A., BDS, MSc</creatorcontrib><creatorcontrib>Moles, David R., PhD, MSc (Hons), MIHPE, DDPH RCS (Eng), FHEA</creatorcontrib><creatorcontrib>Hodgson, Tim A., FDS, FDS (OM) RCS, MRCP (UK), FGDP (UK)</creatorcontrib><creatorcontrib>Porter, Stephen R., PhD, MD, FDSRCS, FDSRCSE</creatorcontrib><creatorcontrib>Fedele, Stefano, DDS, PhD</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Academy of Dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Al Johani, Khalid A., BDS, MSc</au><au>Moles, David R., PhD, MSc (Hons), MIHPE, DDPH RCS (Eng), FHEA</au><au>Hodgson, Tim A., FDS, FDS (OM) RCS, MRCP (UK), FGDP (UK)</au><au>Porter, Stephen R., PhD, MD, FDSRCS, FDSRCSE</au><au>Fedele, Stefano, DDS, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Orofacial granulomatosis: Clinical features and long-term outcome of therapy</atitle><jtitle>Journal of the American Academy of Dermatology</jtitle><addtitle>J Am Acad Dermatol</addtitle><date>2010-04-01</date><risdate>2010</risdate><volume>62</volume><issue>4</issue><spage>611</spage><epage>620</epage><pages>611-620</pages><issn>0190-9622</issn><eissn>1097-6787</eissn><coden>JAADDB</coden><abstract>Background Orofacial granulomatosis (OFG) is a chronic inflammatory disorder characterized by persistent or recurrent soft tissue enlargement, oral ulceration, and a variety of other orofacial features. There remain few detailed reports of the clinical features and long-term response to therapy of substantial groups of patients with OFG. Objective The aim of this study was to determine retrospectively the clinical, hematologic, and histopathological features of a large case series of patients with OFG. In addition the long-term response to therapy was examined. Methods Clinically relevant data of 49 patients with OFG who attended a single oral medicine unit in the United Kingdom were retrospectively examined. The analyzed parameters included diagnostic features, clinical manifestations, and outcomes and adverse side effects of therapy. Results Labial swelling was the most common presenting clinical feature at diagnosis (75.5%), followed by intraoral mucosal features other than ulceration such as cobblestoning and gingival enlargement (73.5%). Mucosal ulceration was observed in 36.7% of patients whereas extraoral facial manifestations such as cutaneous erythema and swelling were present in 40.8% of patients. Of the 45 patients who required treatment, 24 (53.3%) were treated with topical corticosteroids/immunosuppressants only, whereas 21 (46.7%) received a combined therapy (topical plus systemic corticosteroids/immunosuppressants and/or intralesional corticosteroids). The long-term outcome analysis showed complete/partial resolution of tissue swelling and oral ulceration in 78.8% and 70% of patients, respectively. Limitations The main limitation of the current study was its retrospective design and methodology including differences in reporting clinical features and outcome. Conclusions OFG can show multiple facial and mucosal clinical features. Long-term treatment with topical and/or combined therapy is needed in the majority of patients. Response to therapy is highly variable even though in the long-term complete/partial disease resolution can be obtained in the majority of patients. Mucosal ulceration tends to be more recalcitrant than orofacial swelling. Adverse side effects of therapy are rare.</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>20137827</pmid><doi>10.1016/j.jaad.2009.03.051</doi><tpages>10</tpages></addata></record>
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subjects Adolescent
Adult
Aged
Biological and medical sciences
Child
clinical features
Dermatology
Female
Granulomatosis, Orofacial - diagnosis
Granulomatosis, Orofacial - drug therapy
Humans
long-term outcome
Male
Medical sciences
Middle Aged
orofacial granulomatosis
Retrospective Studies
Time Factors
Treatment Outcome
Young Adult
title Orofacial granulomatosis: Clinical features and long-term outcome of therapy
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