Pachydermodactyly: a rare form of digital fibromatosis-report of four cases
Summary We report four patients with pachydermodactyly, a rare and poorly recognized form of digital fibromatosis characterized by asymptomatic soft‐tissue swelling around one or more proximal interphalangeal joint in young men.
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Veröffentlicht in: | Clinical and experimental dermatology 1991-03, Vol.16 (2), p.121-123 |
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container_title | Clinical and experimental dermatology |
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creator | CURLEY, R.K. HUDSON, P.M. MARSDEN, R.A. |
description | Summary
We report four patients with pachydermodactyly, a rare and poorly recognized form of digital fibromatosis characterized by asymptomatic soft‐tissue swelling around one or more proximal interphalangeal joint in young men. |
doi_str_mv | 10.1111/j.1365-2230.1991.tb00321.x |
format | Article |
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We report four patients with pachydermodactyly, a rare and poorly recognized form of digital fibromatosis characterized by asymptomatic soft‐tissue swelling around one or more proximal interphalangeal joint in young men.</description><identifier>ISSN: 0307-6938</identifier><identifier>EISSN: 1365-2230</identifier><identifier>DOI: 10.1111/j.1365-2230.1991.tb00321.x</identifier><identifier>PMID: 2032373</identifier><identifier>CODEN: CEDEDE</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Biological and medical sciences ; Dermatology ; Fibroma - diagnosis ; Fibroma - pathology ; Fingers - pathology ; Humans ; Male ; Medical sciences ; Soft Tissue Neoplasms - diagnosis ; Soft Tissue Neoplasms - pathology</subject><ispartof>Clinical and experimental dermatology, 1991-03, Vol.16 (2), p.121-123</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4171-15bd71b3d8ce815eeeb7167c2827e9e699c6d66e7cbb5e072e7199e3dc91fe7f3</citedby><cites>FETCH-LOGICAL-c4171-15bd71b3d8ce815eeeb7167c2827e9e699c6d66e7cbb5e072e7199e3dc91fe7f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5440709$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2032373$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CURLEY, R.K.</creatorcontrib><creatorcontrib>HUDSON, P.M.</creatorcontrib><creatorcontrib>MARSDEN, R.A.</creatorcontrib><title>Pachydermodactyly: a rare form of digital fibromatosis-report of four cases</title><title>Clinical and experimental dermatology</title><addtitle>Clin Exp Dermatol</addtitle><description>Summary
We report four patients with pachydermodactyly, a rare and poorly recognized form of digital fibromatosis characterized by asymptomatic soft‐tissue swelling around one or more proximal interphalangeal joint in young men.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Dermatology</subject><subject>Fibroma - diagnosis</subject><subject>Fibroma - pathology</subject><subject>Fingers - pathology</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Soft Tissue Neoplasms - diagnosis</subject><subject>Soft Tissue Neoplasms - pathology</subject><issn>0307-6938</issn><issn>1365-2230</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkNFP2zAQxq0JxEq3PwEpmtDeUnxxYyc8TBoFCgI2pG3i0XKc8-YuwcVORfPf46hR37kXS_d9953vR8gXoDOIdbaaAeN5mmUsNsoSZl1FKctgtv1AJnvpgEwooyLlJSs-kuMQVpQCA5EfkaMs2plgE3L3qPS_vkbfulrprm_680QlXnlMjPNt4kxS27-2U01ibOVdqzoXbEg9rp3vBtm4jU-0Chg-kUOjmoCfx3dK_lxf_V7cpPc_l7eL7_epnoOAFPKqFlCxutBYQI6IlQAudFZkAkvkZal5zTkKXVU5UpGhiEciq3UJBoVhU_J1l7v27mWDoZOtDRqbRj2j2wRZ0JzPWTxwSs53Ru1dCB6NXHvbKt9LoHIgKVdywCUHXHIgKUeSchuHT8Ytm6rFej86oov66airoFVjvHrWNuxt-XxOBS2j7dvO9mob7N_xAbm4uoQMYkC6C7Chw-0-QPn_kgsmcvn0YykfL-ji4m75Sz6wNy-in3E</recordid><startdate>199103</startdate><enddate>199103</enddate><creator>CURLEY, R.K.</creator><creator>HUDSON, P.M.</creator><creator>MARSDEN, R.A.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</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>7X8</scope></search><sort><creationdate>199103</creationdate><title>Pachydermodactyly: a rare form of digital fibromatosis-report of four cases</title><author>CURLEY, R.K. ; HUDSON, P.M. ; MARSDEN, R.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4171-15bd71b3d8ce815eeeb7167c2827e9e699c6d66e7cbb5e072e7199e3dc91fe7f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Dermatology</topic><topic>Fibroma - diagnosis</topic><topic>Fibroma - pathology</topic><topic>Fingers - pathology</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Soft Tissue Neoplasms - diagnosis</topic><topic>Soft Tissue Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CURLEY, R.K.</creatorcontrib><creatorcontrib>HUDSON, P.M.</creatorcontrib><creatorcontrib>MARSDEN, R.A.</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>MEDLINE - Academic</collection><jtitle>Clinical and experimental dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CURLEY, R.K.</au><au>HUDSON, P.M.</au><au>MARSDEN, R.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pachydermodactyly: a rare form of digital fibromatosis-report of four cases</atitle><jtitle>Clinical and experimental dermatology</jtitle><addtitle>Clin Exp Dermatol</addtitle><date>1991-03</date><risdate>1991</risdate><volume>16</volume><issue>2</issue><spage>121</spage><epage>123</epage><pages>121-123</pages><issn>0307-6938</issn><eissn>1365-2230</eissn><coden>CEDEDE</coden><abstract>Summary
We report four patients with pachydermodactyly, a rare and poorly recognized form of digital fibromatosis characterized by asymptomatic soft‐tissue swelling around one or more proximal interphalangeal joint in young men.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>2032373</pmid><doi>10.1111/j.1365-2230.1991.tb00321.x</doi><tpages>3</tpages></addata></record> |
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subjects | Adult Biological and medical sciences Dermatology Fibroma - diagnosis Fibroma - pathology Fingers - pathology Humans Male Medical sciences Soft Tissue Neoplasms - diagnosis Soft Tissue Neoplasms - pathology |
title | Pachydermodactyly: a rare form of digital fibromatosis-report of four cases |
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