A Second Case of Gobello Nevus Syndrome
An uncommon type of epidermal nevus characterized by hyperpigmented hyperkeratotic bands following a Blaschko-linear pattern and generalized follicular hyperkeratosis were observed in a 17-year-old male patient who additionally showed tufted hair folliculitis on the scalp and clinodactyly of the fif...
Gespeichert in:
Veröffentlicht in: | Case reports in dermatology 2016-04, Vol.8 (1), p.85-90 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 90 |
---|---|
container_issue | 1 |
container_start_page | 85 |
container_title | Case reports in dermatology |
container_volume | 8 |
creator | Tadini, Gianluca Rossi, Luisa Carlotta Faure, Elisa Besagni, Francesca Boneschi, Vinicio Esposito, Susanna Brena, Michela |
description | An uncommon type of epidermal nevus characterized by hyperpigmented hyperkeratotic bands following a Blaschko-linear pattern and generalized follicular hyperkeratosis were observed in a 17-year-old male patient who additionally showed tufted hair folliculitis on the scalp and clinodactyly of the fifth finger of both hands. The combination of epidermal nevus with skeletal abnormalities was first described by Gobello et al. [Dermatology 2000;201:51-55] as a new epidermal nevus syndrome that was named after the first author of this work. Our case shows identical clinical and histopathological features and represents the second case of this rare syndrome reported in the literature. |
doi_str_mv | 10.1159/000445675 |
format | Article |
fullrecord | <record><control><sourceid>pubmed_karge</sourceid><recordid>TN_cdi_karger_primary_445675</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_70fad6bdc271485987154af7c06e665b</doaj_id><sourcerecordid>27194976</sourcerecordid><originalsourceid>FETCH-LOGICAL-c417t-d0ed67f08fb10a944727ea62d2556b375bd80fe8aa19fea6a9e038aebaceb7623</originalsourceid><addsrcrecordid>eNptkM1LAzEQxYMoWqsH7yILHsRDNdnNx-YiyPpVKHpQz2GymdTWbVOyVfC_d-vq0oKnTPJ-8ybzCDli9IIxoS8ppZwLqcQW6TEp04FsLttr9R7Zr-sppVILme2SvVQxzbWSPXJ2nTxjGeYuKaDGJPjkPlisqpA84udHnTx_zV0MMzwgOx6qGg9_zz55vbt9KR4Go6f7YXE9GpScqeXAUXRSeZp7yyhozlWqEGTqUiGkzZSwLqcecwCmfSOARprlgBZKtEqmWZ8MW18XYGoWcTKD-GUCTMzPQ4hjA3E5KSs0inpw0rqy2YbnQueKCQ5elVSilMI2Xlet1-LDztCVOF9GqDZMN5X55M2Mw6fhucx1tvrMeWtQxlDXEX3Xy6hZJW-65Bv2ZH1YR_5F3QDHLfAOcYyxA7r-03_l4ua2JczC-ewbdpaSWw</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>A Second Case of Gobello Nevus Syndrome</title><source>PubMed Central</source><source>Directory of Open Access Journals</source><source>EZB Electronic Journals Library</source><source>Karger Open Access</source><creator>Tadini, Gianluca ; Rossi, Luisa Carlotta ; Faure, Elisa ; Besagni, Francesca ; Boneschi, Vinicio ; Esposito, Susanna ; Brena, Michela</creator><creatorcontrib>Tadini, Gianluca ; Rossi, Luisa Carlotta ; Faure, Elisa ; Besagni, Francesca ; Boneschi, Vinicio ; Esposito, Susanna ; Brena, Michela</creatorcontrib><description>An uncommon type of epidermal nevus characterized by hyperpigmented hyperkeratotic bands following a Blaschko-linear pattern and generalized follicular hyperkeratosis were observed in a 17-year-old male patient who additionally showed tufted hair folliculitis on the scalp and clinodactyly of the fifth finger of both hands. The combination of epidermal nevus with skeletal abnormalities was first described by Gobello et al. [Dermatology 2000;201:51-55] as a new epidermal nevus syndrome that was named after the first author of this work. Our case shows identical clinical and histopathological features and represents the second case of this rare syndrome reported in the literature.</description><identifier>ISSN: 1662-6567</identifier><identifier>EISSN: 1662-6567</identifier><identifier>DOI: 10.1159/000445675</identifier><identifier>PMID: 27194976</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Bone abnormalities ; Clinodactyly ; Epidermal nevus syndrome ; Follicular hyperkeratosis ; Published: April 2016 ; Tufted hair folliculitis</subject><ispartof>Case reports in dermatology, 2016-04, Vol.8 (1), p.85-90</ispartof><rights>2016 The Author(s). Published by S. Karger AG, Basel</rights><rights>Copyright © 2016 by S. Karger AG, Basel 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c417t-d0ed67f08fb10a944727ea62d2556b375bd80fe8aa19fea6a9e038aebaceb7623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868932/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868932/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,27635,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27194976$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tadini, Gianluca</creatorcontrib><creatorcontrib>Rossi, Luisa Carlotta</creatorcontrib><creatorcontrib>Faure, Elisa</creatorcontrib><creatorcontrib>Besagni, Francesca</creatorcontrib><creatorcontrib>Boneschi, Vinicio</creatorcontrib><creatorcontrib>Esposito, Susanna</creatorcontrib><creatorcontrib>Brena, Michela</creatorcontrib><title>A Second Case of Gobello Nevus Syndrome</title><title>Case reports in dermatology</title><addtitle>Case Rep Dermatol</addtitle><description>An uncommon type of epidermal nevus characterized by hyperpigmented hyperkeratotic bands following a Blaschko-linear pattern and generalized follicular hyperkeratosis were observed in a 17-year-old male patient who additionally showed tufted hair folliculitis on the scalp and clinodactyly of the fifth finger of both hands. The combination of epidermal nevus with skeletal abnormalities was first described by Gobello et al. [Dermatology 2000;201:51-55] as a new epidermal nevus syndrome that was named after the first author of this work. Our case shows identical clinical and histopathological features and represents the second case of this rare syndrome reported in the literature.</description><subject>Bone abnormalities</subject><subject>Clinodactyly</subject><subject>Epidermal nevus syndrome</subject><subject>Follicular hyperkeratosis</subject><subject>Published: April 2016</subject><subject>Tufted hair folliculitis</subject><issn>1662-6567</issn><issn>1662-6567</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>M--</sourceid><sourceid>DOA</sourceid><recordid>eNptkM1LAzEQxYMoWqsH7yILHsRDNdnNx-YiyPpVKHpQz2GymdTWbVOyVfC_d-vq0oKnTPJ-8ybzCDli9IIxoS8ppZwLqcQW6TEp04FsLttr9R7Zr-sppVILme2SvVQxzbWSPXJ2nTxjGeYuKaDGJPjkPlisqpA84udHnTx_zV0MMzwgOx6qGg9_zz55vbt9KR4Go6f7YXE9GpScqeXAUXRSeZp7yyhozlWqEGTqUiGkzZSwLqcecwCmfSOARprlgBZKtEqmWZ8MW18XYGoWcTKD-GUCTMzPQ4hjA3E5KSs0inpw0rqy2YbnQueKCQ5elVSilMI2Xlet1-LDztCVOF9GqDZMN5X55M2Mw6fhucx1tvrMeWtQxlDXEX3Xy6hZJW-65Bv2ZH1YR_5F3QDHLfAOcYyxA7r-03_l4ua2JczC-ewbdpaSWw</recordid><startdate>20160420</startdate><enddate>20160420</enddate><creator>Tadini, Gianluca</creator><creator>Rossi, Luisa Carlotta</creator><creator>Faure, Elisa</creator><creator>Besagni, Francesca</creator><creator>Boneschi, Vinicio</creator><creator>Esposito, Susanna</creator><creator>Brena, Michela</creator><general>S. Karger AG</general><general>Karger Publishers</general><scope>M--</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20160420</creationdate><title>A Second Case of Gobello Nevus Syndrome</title><author>Tadini, Gianluca ; Rossi, Luisa Carlotta ; Faure, Elisa ; Besagni, Francesca ; Boneschi, Vinicio ; Esposito, Susanna ; Brena, Michela</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-d0ed67f08fb10a944727ea62d2556b375bd80fe8aa19fea6a9e038aebaceb7623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Bone abnormalities</topic><topic>Clinodactyly</topic><topic>Epidermal nevus syndrome</topic><topic>Follicular hyperkeratosis</topic><topic>Published: April 2016</topic><topic>Tufted hair folliculitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tadini, Gianluca</creatorcontrib><creatorcontrib>Rossi, Luisa Carlotta</creatorcontrib><creatorcontrib>Faure, Elisa</creatorcontrib><creatorcontrib>Besagni, Francesca</creatorcontrib><creatorcontrib>Boneschi, Vinicio</creatorcontrib><creatorcontrib>Esposito, Susanna</creatorcontrib><creatorcontrib>Brena, Michela</creatorcontrib><collection>Karger Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Case reports in dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tadini, Gianluca</au><au>Rossi, Luisa Carlotta</au><au>Faure, Elisa</au><au>Besagni, Francesca</au><au>Boneschi, Vinicio</au><au>Esposito, Susanna</au><au>Brena, Michela</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Second Case of Gobello Nevus Syndrome</atitle><jtitle>Case reports in dermatology</jtitle><addtitle>Case Rep Dermatol</addtitle><date>2016-04-20</date><risdate>2016</risdate><volume>8</volume><issue>1</issue><spage>85</spage><epage>90</epage><pages>85-90</pages><issn>1662-6567</issn><eissn>1662-6567</eissn><abstract>An uncommon type of epidermal nevus characterized by hyperpigmented hyperkeratotic bands following a Blaschko-linear pattern and generalized follicular hyperkeratosis were observed in a 17-year-old male patient who additionally showed tufted hair folliculitis on the scalp and clinodactyly of the fifth finger of both hands. The combination of epidermal nevus with skeletal abnormalities was first described by Gobello et al. [Dermatology 2000;201:51-55] as a new epidermal nevus syndrome that was named after the first author of this work. Our case shows identical clinical and histopathological features and represents the second case of this rare syndrome reported in the literature.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>27194976</pmid><doi>10.1159/000445675</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1662-6567 |
ispartof | Case reports in dermatology, 2016-04, Vol.8 (1), p.85-90 |
issn | 1662-6567 1662-6567 |
language | eng |
recordid | cdi_karger_primary_445675 |
source | PubMed Central; Directory of Open Access Journals; EZB Electronic Journals Library; Karger Open Access |
subjects | Bone abnormalities Clinodactyly Epidermal nevus syndrome Follicular hyperkeratosis Published: April 2016 Tufted hair folliculitis |
title | A Second Case of Gobello Nevus Syndrome |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T07%3A33%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_karge&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Second%20Case%20of%20Gobello%20Nevus%20Syndrome&rft.jtitle=Case%20reports%20in%20dermatology&rft.au=Tadini,%20Gianluca&rft.date=2016-04-20&rft.volume=8&rft.issue=1&rft.spage=85&rft.epage=90&rft.pages=85-90&rft.issn=1662-6567&rft.eissn=1662-6567&rft_id=info:doi/10.1159/000445675&rft_dat=%3Cpubmed_karge%3E27194976%3C/pubmed_karge%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/27194976&rft_doaj_id=oai_doaj_org_article_70fad6bdc271485987154af7c06e665b&rfr_iscdi=true |