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Rosetoid schwannoma (neuroblastoma‐like) in association with an anetoderma
Background: We report an additional case of an extremely uncommon but distinctive histological variant of benign schwannoma, which was previously designated as neuroblastoma‐like schwannoma by Goldblum et al. Methods: A 29‐year‐old woman referred to a 6‐year‐history of an atrofic macule. Its clini...
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| Published in: | Journal of cutaneous pathology 2006-08, Vol.33 (8), p.573-576 |
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| cites | cdi_FETCH-LOGICAL-c4270-ea4d8b63a3e6fe42f9a77e938f2ec77cf4159690514c22c3637e22fe3b0e1dff3 |
| container_end_page | 576 |
| container_issue | 8 |
| container_start_page | 573 |
| container_title | Journal of cutaneous pathology |
| container_volume | 33 |
| creator | Vélez, Dolores Reina Duran, Teresa Pérez‐Gala, Silvia Fernández, Javier Fraga |
| description | Background: We report an additional case of an extremely uncommon but distinctive histological variant of benign schwannoma, which was previously designated as neuroblastoma‐like schwannoma by Goldblum et al.
Methods: A 29‐year‐old woman referred to a 6‐year‐history of an atrofic macule. Its clinical appearance was similar to that of an anetoderma.
Results: A cutaneous biopsy showed findings consistent with a neuroblastoma‐like schwannoma with the following peculiar features: (i) Being fully composed of rosette‐like structures. (ii) Association to an anetoderma.
Conclusions: Because neither the histological pattern nor the type of tumor allows a differential diagnosis with neuroblastoma, we propose the descriptive term of rosetoid schwannoma. And to our knowledge, this will be the first case reported of rosetoid schwannoma associated to anetoderma. |
| doi_str_mv | 10.1111/j.1600-0560.2006.00480.x |
| format | article |
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Methods: A 29‐year‐old woman referred to a 6‐year‐history of an atrofic macule. Its clinical appearance was similar to that of an anetoderma.
Results: A cutaneous biopsy showed findings consistent with a neuroblastoma‐like schwannoma with the following peculiar features: (i) Being fully composed of rosette‐like structures. (ii) Association to an anetoderma.
Conclusions: Because neither the histological pattern nor the type of tumor allows a differential diagnosis with neuroblastoma, we propose the descriptive term of rosetoid schwannoma. And to our knowledge, this will be the first case reported of rosetoid schwannoma associated to anetoderma.</description><identifier>ISSN: 0303-6987</identifier><identifier>EISSN: 1600-0560</identifier><identifier>DOI: 10.1111/j.1600-0560.2006.00480.x</identifier><identifier>PMID: 16919032</identifier><identifier>CODEN: JCUPBN</identifier><language>eng</language><publisher>Oxford, UK; Malden, USA: Blackwell Publishing Ltd</publisher><subject>Adult ; Biological and medical sciences ; Dermatology ; Elastic Tissue - pathology ; Female ; Humans ; Medical sciences ; Neurilemmoma - chemistry ; Neurilemmoma - complications ; Neurilemmoma - pathology ; Neurology ; S100 Proteins - analysis ; Skin Diseases - complications ; Skin Diseases - pathology ; Tumors of the nervous system. Phacomatoses</subject><ispartof>Journal of cutaneous pathology, 2006-08, Vol.33 (8), p.573-576</ispartof><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4270-ea4d8b63a3e6fe42f9a77e938f2ec77cf4159690514c22c3637e22fe3b0e1dff3</citedby><cites>FETCH-LOGICAL-c4270-ea4d8b63a3e6fe42f9a77e938f2ec77cf4159690514c22c3637e22fe3b0e1dff3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18045226$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16919032$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vélez, Dolores</creatorcontrib><creatorcontrib>Reina Duran, Teresa</creatorcontrib><creatorcontrib>Pérez‐Gala, Silvia</creatorcontrib><creatorcontrib>Fernández, Javier Fraga</creatorcontrib><title>Rosetoid schwannoma (neuroblastoma‐like) in association with an anetoderma</title><title>Journal of cutaneous pathology</title><addtitle>J Cutan Pathol</addtitle><description>Background: We report an additional case of an extremely uncommon but distinctive histological variant of benign schwannoma, which was previously designated as neuroblastoma‐like schwannoma by Goldblum et al.
Methods: A 29‐year‐old woman referred to a 6‐year‐history of an atrofic macule. Its clinical appearance was similar to that of an anetoderma.
Results: A cutaneous biopsy showed findings consistent with a neuroblastoma‐like schwannoma with the following peculiar features: (i) Being fully composed of rosette‐like structures. (ii) Association to an anetoderma.
Conclusions: Because neither the histological pattern nor the type of tumor allows a differential diagnosis with neuroblastoma, we propose the descriptive term of rosetoid schwannoma. And to our knowledge, this will be the first case reported of rosetoid schwannoma associated to anetoderma.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Dermatology</subject><subject>Elastic Tissue - pathology</subject><subject>Female</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Neurilemmoma - chemistry</subject><subject>Neurilemmoma - complications</subject><subject>Neurilemmoma - pathology</subject><subject>Neurology</subject><subject>S100 Proteins - analysis</subject><subject>Skin Diseases - complications</subject><subject>Skin Diseases - pathology</subject><subject>Tumors of the nervous system. Phacomatoses</subject><issn>0303-6987</issn><issn>1600-0560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqNkMtO3DAUhi1UVAboK6BsimCR9PgSx5G6QaNekEYCVcza8jjHGk-TmMYZDez6CDwjT4KnM4Il9cY-9vcfH32EZBQKmtaXVUElQA6lhIIByAJAKCgeDsjk9eEDmQAHnstaVUfkOMYVAJVKlh_JEZU1rYGzCZn9ChHH4Jss2uXG9H3oTHbR43oIi9bEMZXPf59a_xsvM99nJsZgvRl96LONH5eZSXd9atDg0JlTcuhMG_HTfj8h8-_f7qY_89nNj-vp1Sy3glWQoxGNWkhuOEqHgrnaVBXWXDmGtqqsE7SsZQ0lFZYxyyWvkDGHfAFIG-f4CTnf9b0fwp81xlF3Plps2zRKWEctVZXiVLwL0lrIUkmeQLUD7RBiHNDp-8F3ZnjUFPRWuV7prVm9Nau3yvU_5fohRc_2f6wXHTZvwb3jBHzeAyZa07rB9NbHN06BKBmTifu64za-xcf_HkBP57fpwF8AZ_SdKQ</recordid><startdate>200608</startdate><enddate>200608</enddate><creator>Vélez, Dolores</creator><creator>Reina Duran, Teresa</creator><creator>Pérez‐Gala, Silvia</creator><creator>Fernández, Javier Fraga</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>200608</creationdate><title>Rosetoid schwannoma (neuroblastoma‐like) in association with an anetoderma</title><author>Vélez, Dolores ; Reina Duran, Teresa ; Pérez‐Gala, Silvia ; Fernández, Javier Fraga</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4270-ea4d8b63a3e6fe42f9a77e938f2ec77cf4159690514c22c3637e22fe3b0e1dff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Dermatology</topic><topic>Elastic Tissue - pathology</topic><topic>Female</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Neurilemmoma - chemistry</topic><topic>Neurilemmoma - complications</topic><topic>Neurilemmoma - pathology</topic><topic>Neurology</topic><topic>S100 Proteins - analysis</topic><topic>Skin Diseases - complications</topic><topic>Skin Diseases - pathology</topic><topic>Tumors of the nervous system. Phacomatoses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vélez, Dolores</creatorcontrib><creatorcontrib>Reina Duran, Teresa</creatorcontrib><creatorcontrib>Pérez‐Gala, Silvia</creatorcontrib><creatorcontrib>Fernández, Javier Fraga</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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cutaneous pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vélez, Dolores</au><au>Reina Duran, Teresa</au><au>Pérez‐Gala, Silvia</au><au>Fernández, Javier Fraga</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rosetoid schwannoma (neuroblastoma‐like) in association with an anetoderma</atitle><jtitle>Journal of cutaneous pathology</jtitle><addtitle>J Cutan Pathol</addtitle><date>2006-08</date><risdate>2006</risdate><volume>33</volume><issue>8</issue><spage>573</spage><epage>576</epage><pages>573-576</pages><issn>0303-6987</issn><eissn>1600-0560</eissn><coden>JCUPBN</coden><abstract>Background: We report an additional case of an extremely uncommon but distinctive histological variant of benign schwannoma, which was previously designated as neuroblastoma‐like schwannoma by Goldblum et al.
Methods: A 29‐year‐old woman referred to a 6‐year‐history of an atrofic macule. Its clinical appearance was similar to that of an anetoderma.
Results: A cutaneous biopsy showed findings consistent with a neuroblastoma‐like schwannoma with the following peculiar features: (i) Being fully composed of rosette‐like structures. (ii) Association to an anetoderma.
Conclusions: Because neither the histological pattern nor the type of tumor allows a differential diagnosis with neuroblastoma, we propose the descriptive term of rosetoid schwannoma. And to our knowledge, this will be the first case reported of rosetoid schwannoma associated to anetoderma.</abstract><cop>Oxford, UK; Malden, USA</cop><pub>Blackwell Publishing Ltd</pub><pmid>16919032</pmid><doi>10.1111/j.1600-0560.2006.00480.x</doi><tpages>4</tpages></addata></record> |
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| ispartof | Journal of cutaneous pathology, 2006-08, Vol.33 (8), p.573-576 |
| issn | 0303-6987 1600-0560 |
| language | eng |
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| source | Wiley:Jisc Collections:Wiley Read and Publish Open Access 2024-2025 (reading list) |
| subjects | Adult Biological and medical sciences Dermatology Elastic Tissue - pathology Female Humans Medical sciences Neurilemmoma - chemistry Neurilemmoma - complications Neurilemmoma - pathology Neurology S100 Proteins - analysis Skin Diseases - complications Skin Diseases - pathology Tumors of the nervous system. Phacomatoses |
| title | Rosetoid schwannoma (neuroblastoma‐like) in association with an anetoderma |
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