Facial porokeratosis characterized by destructive lesions

Porokeratosis is a rare group of keratinizing diseases. It is inherited as an autosomal dominant disease with variable penetrance, although sporadic cases are often reported. Porokeratosis has as its histological hallmark the typical cornoid lamella. Porokeratosis lesions localized on the face can v...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of dermatology 2004-12, Vol.43 (12), p.913-914
Hauptverfasser: Miranda, Sandra Maria Bitencourt, De Miranda, João Nestor Rodrigues, De Souza Filho, João Basílio
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 914
container_issue 12
container_start_page 913
container_title International journal of dermatology
container_volume 43
creator Miranda, Sandra Maria Bitencourt
De Miranda, João Nestor Rodrigues
De Souza Filho, João Basílio
description Porokeratosis is a rare group of keratinizing diseases. It is inherited as an autosomal dominant disease with variable penetrance, although sporadic cases are often reported. Porokeratosis has as its histological hallmark the typical cornoid lamella. Porokeratosis lesions localized on the face can vary from superficial to destructive in nature. Only 12 cases have been reported in the literature to date. We report one more unusual case of destructive facial porokeratosis.
doi_str_mv 10.1111/j.1365-4632.2004.02315.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67123513</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>762803111</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4625-c0dbf259a790270ff9a31536af87afe1eea6bad938298d2ef9eb0efc16766373</originalsourceid><addsrcrecordid>eNqNkM1u1DAURq0K1A4Dr1BFleguwT-xEy9YoJaWQlUkVEF31o1zrXqamUztBGZ4ehxm1Eqs8Ma-8vmuPh1CMkYLls67RcGEknmpBC84pWVBuWCy2ByQ2dPHCzKjlLFcU6mPyKsYF2kUnJWH5IhJqTRlakb0BVgPXbbuQ_-AAYY--pjZewhgBwz-N7ZZs81ajEMY7eB_YtZh9P0qviYvHXQR3-zvObm9-Hh79im__np5dfbhOrel4jK3tG0clxoqTXlFndOQqgoFrq7AIUME1UCrRc113XJ0GhuKzjJVKSUqMSenu7Xr0D-OqYZZ-mix62CF_RiNqhgXkokEnvwDLvoxrFI1wzmvdVklK3NS7yAb-hgDOrMOfglhaxg1k1qzMJNBMxk0k1rzV63ZpOjxfv_YLLF9Du5dJuDtHoBooXMBVtbHZ04JKkUtE_d-x_3yHW7_u4C5-nw-vVI-3-V9HHDzlIfwkGSISpofN5dGyrvv6ubLN8PFH5etovE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>222894746</pqid></control><display><type>article</type><title>Facial porokeratosis characterized by destructive lesions</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Miranda, Sandra Maria Bitencourt ; De Miranda, João Nestor Rodrigues ; De Souza Filho, João Basílio</creator><creatorcontrib>Miranda, Sandra Maria Bitencourt ; De Miranda, João Nestor Rodrigues ; De Souza Filho, João Basílio</creatorcontrib><description>Porokeratosis is a rare group of keratinizing diseases. It is inherited as an autosomal dominant disease with variable penetrance, although sporadic cases are often reported. Porokeratosis has as its histological hallmark the typical cornoid lamella. Porokeratosis lesions localized on the face can vary from superficial to destructive in nature. Only 12 cases have been reported in the literature to date. We report one more unusual case of destructive facial porokeratosis.</description><identifier>ISSN: 0011-9059</identifier><identifier>EISSN: 1365-4632</identifier><identifier>DOI: 10.1111/j.1365-4632.2004.02315.x</identifier><identifier>PMID: 15569016</identifier><identifier>CODEN: IJDEBB</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Adult ; Biological and medical sciences ; Dermatology ; Diagnosis, Differential ; Dyskeratosis ; Facial Dermatoses - diagnosis ; Humans ; Lip Diseases - diagnosis ; Male ; Medical sciences ; Nose Diseases - diagnosis ; Porokeratosis - diagnosis</subject><ispartof>International journal of dermatology, 2004-12, Vol.43 (12), p.913-914</ispartof><rights>2005 INIST-CNRS</rights><rights>Copyright Blackwell Scientific Publications Ltd. Dec 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4625-c0dbf259a790270ff9a31536af87afe1eea6bad938298d2ef9eb0efc16766373</citedby><cites>FETCH-LOGICAL-c4625-c0dbf259a790270ff9a31536af87afe1eea6bad938298d2ef9eb0efc16766373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-4632.2004.02315.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-4632.2004.02315.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16305385$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15569016$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miranda, Sandra Maria Bitencourt</creatorcontrib><creatorcontrib>De Miranda, João Nestor Rodrigues</creatorcontrib><creatorcontrib>De Souza Filho, João Basílio</creatorcontrib><title>Facial porokeratosis characterized by destructive lesions</title><title>International journal of dermatology</title><addtitle>Int J Dermatol</addtitle><description>Porokeratosis is a rare group of keratinizing diseases. It is inherited as an autosomal dominant disease with variable penetrance, although sporadic cases are often reported. Porokeratosis has as its histological hallmark the typical cornoid lamella. Porokeratosis lesions localized on the face can vary from superficial to destructive in nature. Only 12 cases have been reported in the literature to date. We report one more unusual case of destructive facial porokeratosis.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Dermatology</subject><subject>Diagnosis, Differential</subject><subject>Dyskeratosis</subject><subject>Facial Dermatoses - diagnosis</subject><subject>Humans</subject><subject>Lip Diseases - diagnosis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Nose Diseases - diagnosis</subject><subject>Porokeratosis - diagnosis</subject><issn>0011-9059</issn><issn>1365-4632</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkM1u1DAURq0K1A4Dr1BFleguwT-xEy9YoJaWQlUkVEF31o1zrXqamUztBGZ4ehxm1Eqs8Ma-8vmuPh1CMkYLls67RcGEknmpBC84pWVBuWCy2ByQ2dPHCzKjlLFcU6mPyKsYF2kUnJWH5IhJqTRlakb0BVgPXbbuQ_-AAYY--pjZewhgBwz-N7ZZs81ajEMY7eB_YtZh9P0qviYvHXQR3-zvObm9-Hh79im__np5dfbhOrel4jK3tG0clxoqTXlFndOQqgoFrq7AIUME1UCrRc113XJ0GhuKzjJVKSUqMSenu7Xr0D-OqYZZ-mix62CF_RiNqhgXkokEnvwDLvoxrFI1wzmvdVklK3NS7yAb-hgDOrMOfglhaxg1k1qzMJNBMxk0k1rzV63ZpOjxfv_YLLF9Du5dJuDtHoBooXMBVtbHZ04JKkUtE_d-x_3yHW7_u4C5-nw-vVI-3-V9HHDzlIfwkGSISpofN5dGyrvv6ubLN8PFH5etovE</recordid><startdate>200412</startdate><enddate>200412</enddate><creator>Miranda, Sandra Maria Bitencourt</creator><creator>De Miranda, João Nestor Rodrigues</creator><creator>De Souza Filho, João Basílio</creator><general>Blackwell Science Ltd</general><general>Blackwell Science</general><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><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>7T5</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200412</creationdate><title>Facial porokeratosis characterized by destructive lesions</title><author>Miranda, Sandra Maria Bitencourt ; De Miranda, João Nestor Rodrigues ; De Souza Filho, João Basílio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4625-c0dbf259a790270ff9a31536af87afe1eea6bad938298d2ef9eb0efc16766373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Dermatology</topic><topic>Diagnosis, Differential</topic><topic>Dyskeratosis</topic><topic>Facial Dermatoses - diagnosis</topic><topic>Humans</topic><topic>Lip Diseases - diagnosis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nose Diseases - diagnosis</topic><topic>Porokeratosis - diagnosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miranda, Sandra Maria Bitencourt</creatorcontrib><creatorcontrib>De Miranda, João Nestor Rodrigues</creatorcontrib><creatorcontrib>De Souza Filho, João Basílio</creatorcontrib><collection>Istex</collection><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>Immunology Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miranda, Sandra Maria Bitencourt</au><au>De Miranda, João Nestor Rodrigues</au><au>De Souza Filho, João Basílio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Facial porokeratosis characterized by destructive lesions</atitle><jtitle>International journal of dermatology</jtitle><addtitle>Int J Dermatol</addtitle><date>2004-12</date><risdate>2004</risdate><volume>43</volume><issue>12</issue><spage>913</spage><epage>914</epage><pages>913-914</pages><issn>0011-9059</issn><eissn>1365-4632</eissn><coden>IJDEBB</coden><abstract>Porokeratosis is a rare group of keratinizing diseases. It is inherited as an autosomal dominant disease with variable penetrance, although sporadic cases are often reported. Porokeratosis has as its histological hallmark the typical cornoid lamella. Porokeratosis lesions localized on the face can vary from superficial to destructive in nature. Only 12 cases have been reported in the literature to date. We report one more unusual case of destructive facial porokeratosis.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>15569016</pmid><doi>10.1111/j.1365-4632.2004.02315.x</doi><tpages>2</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0011-9059
ispartof International journal of dermatology, 2004-12, Vol.43 (12), p.913-914
issn 0011-9059
1365-4632
language eng
recordid cdi_proquest_miscellaneous_67123513
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Adult
Biological and medical sciences
Dermatology
Diagnosis, Differential
Dyskeratosis
Facial Dermatoses - diagnosis
Humans
Lip Diseases - diagnosis
Male
Medical sciences
Nose Diseases - diagnosis
Porokeratosis - diagnosis
title Facial porokeratosis characterized by destructive lesions
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T12%3A10%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Facial%20porokeratosis%20characterized%20by%20destructive%20lesions&rft.jtitle=International%20journal%20of%20dermatology&rft.au=Miranda,%20Sandra%20Maria%20Bitencourt&rft.date=2004-12&rft.volume=43&rft.issue=12&rft.spage=913&rft.epage=914&rft.pages=913-914&rft.issn=0011-9059&rft.eissn=1365-4632&rft.coden=IJDEBB&rft_id=info:doi/10.1111/j.1365-4632.2004.02315.x&rft_dat=%3Cproquest_cross%3E762803111%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=222894746&rft_id=info:pmid/15569016&rfr_iscdi=true