Palisaded Neutrophilic and Granulomatous Dermatitis in a Patient with Behçet’s Disease: A Case Report
Palisaded neutrophilic and granulomatous dermatitis (PNGD) is an uncommon skin eruption and characterized histopatho-logically by the presence of granulomatous inflammation with or without leukocytoclastic vasculitis. PNGD is known to be associated with various immune-mediated connective tissue dise...
Gespeichert in:
Veröffentlicht in: | Annals of dermatology 2021-02, Vol.33 (1), p.73 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | kor |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 1 |
container_start_page | 73 |
container_title | Annals of dermatology |
container_volume | 33 |
creator | Young-bin Shin Jeong-won Jo Tae-jin Yoon |
description | Palisaded neutrophilic and granulomatous dermatitis (PNGD) is an uncommon skin eruption and characterized histopatho-logically by the presence of granulomatous inflammation with or without leukocytoclastic vasculitis. PNGD is known to be associated with various immune-mediated connective tissue diseases such as rheumatoid arthritis and lupus erythematosus. However, to our knowledge, a case of PNGD in a patient with Behçet’s disease is extremely rare and only one case has been reported in foreign literature to date. Herein, we report an unusual case of a 60-year-old female with Behçet’s disease who presented multiple erythematous to flesh-colored papules on the extremities, buttocks, and ear lobes and was diagnosed with PNGD. After the treatment of systemic corticosteroids, colchicine and azathioprine, the skin lesions and oral ulcers improved. The patient is under observation without recurrence of skin lesions for 6 months. (Ann Dermatol 33(1) 73∼76, 2021) |
format | Article |
fullrecord | <record><control><sourceid>kiss</sourceid><recordid>TN_cdi_kiss_primary_3846028</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><kiss_id>3846028</kiss_id><sourcerecordid>3846028</sourcerecordid><originalsourceid>FETCH-kiss_primary_38460283</originalsourceid><addsrcrecordid>eNp9ijsKwlAQRR-iYPyswGY2EHhJ_EQ7_1YSxF4GM5LRmIQ3L4id23AFLsSduBJTWFude7inphxf64EbhON-XTme9gJ3rMNRU7VEzloPPX_kOSqJMGXBmGLYUmlNXiSc8hEwi2FtMCvT_Io2LwUWZKrFlgU4A4SoEsos3NgmMKPk_SL7eTyrkIVQaAJTmFeEHRW5sR3VOGEq1P2xrXqr5X6-cS8scigMX9HcD0HYH2o_DP6_X2goRGM</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Palisaded Neutrophilic and Granulomatous Dermatitis in a Patient with Behçet’s Disease: A Case Report</title><source>KoreaMed Synapse</source><source>PubMed Central Free</source><source>KoreaMed Open Access</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Young-bin Shin ; Jeong-won Jo ; Tae-jin Yoon</creator><creatorcontrib>Young-bin Shin ; Jeong-won Jo ; Tae-jin Yoon</creatorcontrib><description>Palisaded neutrophilic and granulomatous dermatitis (PNGD) is an uncommon skin eruption and characterized histopatho-logically by the presence of granulomatous inflammation with or without leukocytoclastic vasculitis. PNGD is known to be associated with various immune-mediated connective tissue diseases such as rheumatoid arthritis and lupus erythematosus. However, to our knowledge, a case of PNGD in a patient with Behçet’s disease is extremely rare and only one case has been reported in foreign literature to date. Herein, we report an unusual case of a 60-year-old female with Behçet’s disease who presented multiple erythematous to flesh-colored papules on the extremities, buttocks, and ear lobes and was diagnosed with PNGD. After the treatment of systemic corticosteroids, colchicine and azathioprine, the skin lesions and oral ulcers improved. The patient is under observation without recurrence of skin lesions for 6 months. (Ann Dermatol 33(1) 73∼76, 2021)</description><identifier>ISSN: 1013-9087</identifier><identifier>EISSN: 2005-3894</identifier><language>kor</language><publisher>대한피부과학회</publisher><subject>Behcet syndrome ; Palisaded neutrophilic granulomatous dermatitis</subject><ispartof>Annals of dermatology, 2021-02, Vol.33 (1), p.73</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785</link.rule.ids></links><search><creatorcontrib>Young-bin Shin</creatorcontrib><creatorcontrib>Jeong-won Jo</creatorcontrib><creatorcontrib>Tae-jin Yoon</creatorcontrib><title>Palisaded Neutrophilic and Granulomatous Dermatitis in a Patient with Behçet’s Disease: A Case Report</title><title>Annals of dermatology</title><addtitle>Annals of Dermatology</addtitle><description>Palisaded neutrophilic and granulomatous dermatitis (PNGD) is an uncommon skin eruption and characterized histopatho-logically by the presence of granulomatous inflammation with or without leukocytoclastic vasculitis. PNGD is known to be associated with various immune-mediated connective tissue diseases such as rheumatoid arthritis and lupus erythematosus. However, to our knowledge, a case of PNGD in a patient with Behçet’s disease is extremely rare and only one case has been reported in foreign literature to date. Herein, we report an unusual case of a 60-year-old female with Behçet’s disease who presented multiple erythematous to flesh-colored papules on the extremities, buttocks, and ear lobes and was diagnosed with PNGD. After the treatment of systemic corticosteroids, colchicine and azathioprine, the skin lesions and oral ulcers improved. The patient is under observation without recurrence of skin lesions for 6 months. (Ann Dermatol 33(1) 73∼76, 2021)</description><subject>Behcet syndrome</subject><subject>Palisaded neutrophilic granulomatous dermatitis</subject><issn>1013-9087</issn><issn>2005-3894</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9ijsKwlAQRR-iYPyswGY2EHhJ_EQ7_1YSxF4GM5LRmIQ3L4id23AFLsSduBJTWFude7inphxf64EbhON-XTme9gJ3rMNRU7VEzloPPX_kOSqJMGXBmGLYUmlNXiSc8hEwi2FtMCvT_Io2LwUWZKrFlgU4A4SoEsos3NgmMKPk_SL7eTyrkIVQaAJTmFeEHRW5sR3VOGEq1P2xrXqr5X6-cS8scigMX9HcD0HYH2o_DP6_X2goRGM</recordid><startdate>20210205</startdate><enddate>20210205</enddate><creator>Young-bin Shin</creator><creator>Jeong-won Jo</creator><creator>Tae-jin Yoon</creator><general>대한피부과학회</general><scope>HZB</scope><scope>Q5X</scope></search><sort><creationdate>20210205</creationdate><title>Palisaded Neutrophilic and Granulomatous Dermatitis in a Patient with Behçet’s Disease: A Case Report</title><author>Young-bin Shin ; Jeong-won Jo ; Tae-jin Yoon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kiss_primary_38460283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2021</creationdate><topic>Behcet syndrome</topic><topic>Palisaded neutrophilic granulomatous dermatitis</topic><toplevel>online_resources</toplevel><creatorcontrib>Young-bin Shin</creatorcontrib><creatorcontrib>Jeong-won Jo</creatorcontrib><creatorcontrib>Tae-jin Yoon</creatorcontrib><collection>Korean Studies Information Service System (KISS)</collection><collection>Korean Studies Information Service System (KISS) B-Type</collection><jtitle>Annals of dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Young-bin Shin</au><au>Jeong-won Jo</au><au>Tae-jin Yoon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Palisaded Neutrophilic and Granulomatous Dermatitis in a Patient with Behçet’s Disease: A Case Report</atitle><jtitle>Annals of dermatology</jtitle><addtitle>Annals of Dermatology</addtitle><date>2021-02-05</date><risdate>2021</risdate><volume>33</volume><issue>1</issue><spage>73</spage><pages>73-</pages><issn>1013-9087</issn><eissn>2005-3894</eissn><abstract>Palisaded neutrophilic and granulomatous dermatitis (PNGD) is an uncommon skin eruption and characterized histopatho-logically by the presence of granulomatous inflammation with or without leukocytoclastic vasculitis. PNGD is known to be associated with various immune-mediated connective tissue diseases such as rheumatoid arthritis and lupus erythematosus. However, to our knowledge, a case of PNGD in a patient with Behçet’s disease is extremely rare and only one case has been reported in foreign literature to date. Herein, we report an unusual case of a 60-year-old female with Behçet’s disease who presented multiple erythematous to flesh-colored papules on the extremities, buttocks, and ear lobes and was diagnosed with PNGD. After the treatment of systemic corticosteroids, colchicine and azathioprine, the skin lesions and oral ulcers improved. The patient is under observation without recurrence of skin lesions for 6 months. (Ann Dermatol 33(1) 73∼76, 2021)</abstract><pub>대한피부과학회</pub><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1013-9087 |
ispartof | Annals of dermatology, 2021-02, Vol.33 (1), p.73 |
issn | 1013-9087 2005-3894 |
language | kor |
recordid | cdi_kiss_primary_3846028 |
source | KoreaMed Synapse; PubMed Central Free; KoreaMed Open Access; EZB-FREE-00999 freely available EZB journals |
subjects | Behcet syndrome Palisaded neutrophilic granulomatous dermatitis |
title | Palisaded Neutrophilic and Granulomatous Dermatitis in a Patient with Behçet’s Disease: A Case Report |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-13T08%3A57%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-kiss&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Palisaded%20Neutrophilic%20and%20Granulomatous%20Dermatitis%20in%20a%20Patient%20with%20Beh%C3%A7et%E2%80%99s%20Disease:%20A%20Case%20Report&rft.jtitle=Annals%20of%20dermatology&rft.au=Young-bin%20Shin&rft.date=2021-02-05&rft.volume=33&rft.issue=1&rft.spage=73&rft.pages=73-&rft.issn=1013-9087&rft.eissn=2005-3894&rft_id=info:doi/&rft_dat=%3Ckiss%3E3846028%3C/kiss%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_kiss_id=3846028&rfr_iscdi=true |