Childhood soft tissue chondroma. Two cases report
Soft tissue chondroma is a rare benign tumour, which is generally seen in adult. It consists of islands of heterotopic cartilaginous tissue and most localised on the hands and the feet. The hypothesis that microtrauma is involved in the aetiology of this condition has yet to find any factual support...
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| Veröffentlicht in: | Tunisie Medicale 2011-04, Vol.89 (4), p.379-382 |
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| container_title | Tunisie Medicale |
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| creator | SMIDA, Mahmoud ABDENAJI, Wajdi DOUIRA-KHOMSI, Wièm NESSIB, Nabil BELLAGHA, Ibtissem MAHER BEN GHACHEM |
| description | Soft tissue chondroma is a rare benign tumour, which is generally seen in adult. It consists of islands of heterotopic cartilaginous tissue and most localised on the hands and the feet. The hypothesis that microtrauma is involved in the aetiology of this condition has yet to find any factual support.
To report two paediatric cases of soft tissue chondroma.
The first is a soft tissue chondroma of the posterior aspect of the left axilla in a 3-year-old boy. CT scans showed a spherical fatty density soft tissue mass without evident calcifications, attaching the infraspinous muscle. The second patient is a 9-year-old girl presented with a right auricular finger soft tissue chondroma. Radiographs showed several punctuated calcifications with adjacent bone scalloping. MRI revealed a lobulated soft tissue mass attaching the flexor tendons. The tumours were entirely removed. Histological examination showed cartilaginous tissue in both cases. At follow-up, the patients had good functions without evidence of recurrence.
Simple excision should suffice to treat soft tissue chondroma but care should be taken to make the excision complete if recurrence are to be avoided. |
| format | Article |
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To report two paediatric cases of soft tissue chondroma.
The first is a soft tissue chondroma of the posterior aspect of the left axilla in a 3-year-old boy. CT scans showed a spherical fatty density soft tissue mass without evident calcifications, attaching the infraspinous muscle. The second patient is a 9-year-old girl presented with a right auricular finger soft tissue chondroma. Radiographs showed several punctuated calcifications with adjacent bone scalloping. MRI revealed a lobulated soft tissue mass attaching the flexor tendons. The tumours were entirely removed. Histological examination showed cartilaginous tissue in both cases. At follow-up, the patients had good functions without evidence of recurrence.
Simple excision should suffice to treat soft tissue chondroma but care should be taken to make the excision complete if recurrence are to be avoided.</description><identifier>ISSN: 0041-4131</identifier><identifier>PMID: 21484690</identifier><identifier>CODEN: TUMEAF</identifier><language>eng ; fre</language><publisher>Tunis: Société tunisienne des sciences médicales</publisher><subject>Axilla - pathology ; Child ; Child, Preschool ; Chondroma - diagnostic imaging ; Chondroma - pathology ; Chondroma - surgery ; Female ; Fingers - pathology ; Generalites ; Humans ; Male ; Pathologie osteoarticulaire ; Radiography ; Sciences biologiques et medicales ; Sciences medicales ; Soft Tissue Neoplasms - diagnostic imaging ; Soft Tissue Neoplasms - pathology ; Soft Tissue Neoplasms - surgery ; Treatment Outcome ; Tumeurs du muscle strié et du squelette</subject><ispartof>Tunisie Medicale, 2011-04, Vol.89 (4), p.379-382</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24472407$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21484690$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SMIDA, Mahmoud</creatorcontrib><creatorcontrib>ABDENAJI, Wajdi</creatorcontrib><creatorcontrib>DOUIRA-KHOMSI, Wièm</creatorcontrib><creatorcontrib>NESSIB, Nabil</creatorcontrib><creatorcontrib>BELLAGHA, Ibtissem</creatorcontrib><creatorcontrib>MAHER BEN GHACHEM</creatorcontrib><title>Childhood soft tissue chondroma. Two cases report</title><title>Tunisie Medicale</title><addtitle>Tunis Med</addtitle><description>Soft tissue chondroma is a rare benign tumour, which is generally seen in adult. It consists of islands of heterotopic cartilaginous tissue and most localised on the hands and the feet. The hypothesis that microtrauma is involved in the aetiology of this condition has yet to find any factual support.
To report two paediatric cases of soft tissue chondroma.
The first is a soft tissue chondroma of the posterior aspect of the left axilla in a 3-year-old boy. CT scans showed a spherical fatty density soft tissue mass without evident calcifications, attaching the infraspinous muscle. The second patient is a 9-year-old girl presented with a right auricular finger soft tissue chondroma. Radiographs showed several punctuated calcifications with adjacent bone scalloping. MRI revealed a lobulated soft tissue mass attaching the flexor tendons. The tumours were entirely removed. Histological examination showed cartilaginous tissue in both cases. At follow-up, the patients had good functions without evidence of recurrence.
Simple excision should suffice to treat soft tissue chondroma but care should be taken to make the excision complete if recurrence are to be avoided.</description><subject>Axilla - pathology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Chondroma - diagnostic imaging</subject><subject>Chondroma - pathology</subject><subject>Chondroma - surgery</subject><subject>Female</subject><subject>Fingers - pathology</subject><subject>Generalites</subject><subject>Humans</subject><subject>Male</subject><subject>Pathologie osteoarticulaire</subject><subject>Radiography</subject><subject>Sciences biologiques et medicales</subject><subject>Sciences medicales</subject><subject>Soft Tissue Neoplasms - diagnostic imaging</subject><subject>Soft Tissue Neoplasms - pathology</subject><subject>Soft Tissue Neoplasms - surgery</subject><subject>Treatment Outcome</subject><subject>Tumeurs du muscle strié et du squelette</subject><issn>0041-4131</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFj0tLxDAUhbNQnGGcvyDZiKtKMknTdCnFFwy46b7c5kErbVNzW8R_b8SKd3MW5-Pj3AuyZ0zyTHLBd-SI-M7SKcbLnF-R3YlLLVXJ9oRXXT_YLgRLMfiFLj3i6qjpwmRjGOGe1p-BGkCHNLo5xOWaXHoY0B23PJD66bGuXrLz2_Nr9XDOZp2zzEEL3hbeMp8rKKUUppDasLYV2iphcp8KKZRsjWbWWG156ZnILTNQujT7QO5-tXMMH6vDpRl7NG4YYHJhxUYrXiRt8UPebOTajs42c-xHiF_N35MJuN0AQAODjzCZHv-5ZDlJVohv9rpZ0A</recordid><startdate>201104</startdate><enddate>201104</enddate><creator>SMIDA, Mahmoud</creator><creator>ABDENAJI, Wajdi</creator><creator>DOUIRA-KHOMSI, Wièm</creator><creator>NESSIB, Nabil</creator><creator>BELLAGHA, Ibtissem</creator><creator>MAHER BEN GHACHEM</creator><general>Société tunisienne des sciences médicales</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201104</creationdate><title>Childhood soft tissue chondroma. Two cases report</title><author>SMIDA, Mahmoud ; ABDENAJI, Wajdi ; DOUIRA-KHOMSI, Wièm ; NESSIB, Nabil ; BELLAGHA, Ibtissem ; MAHER BEN GHACHEM</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p850-eabafd7fd0f56a9443c748c0bb38d63c5f0f54364bc80dcd8d19f035d0ca9e413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng ; fre</language><creationdate>2011</creationdate><topic>Axilla - pathology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Chondroma - diagnostic imaging</topic><topic>Chondroma - pathology</topic><topic>Chondroma - surgery</topic><topic>Female</topic><topic>Fingers - pathology</topic><topic>Generalites</topic><topic>Humans</topic><topic>Male</topic><topic>Pathologie osteoarticulaire</topic><topic>Radiography</topic><topic>Sciences biologiques et medicales</topic><topic>Sciences medicales</topic><topic>Soft Tissue Neoplasms - diagnostic imaging</topic><topic>Soft Tissue Neoplasms - pathology</topic><topic>Soft Tissue Neoplasms - surgery</topic><topic>Treatment Outcome</topic><topic>Tumeurs du muscle strié et du squelette</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SMIDA, Mahmoud</creatorcontrib><creatorcontrib>ABDENAJI, Wajdi</creatorcontrib><creatorcontrib>DOUIRA-KHOMSI, Wièm</creatorcontrib><creatorcontrib>NESSIB, Nabil</creatorcontrib><creatorcontrib>BELLAGHA, Ibtissem</creatorcontrib><creatorcontrib>MAHER BEN GHACHEM</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>MEDLINE - Academic</collection><jtitle>Tunisie Medicale</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SMIDA, Mahmoud</au><au>ABDENAJI, Wajdi</au><au>DOUIRA-KHOMSI, Wièm</au><au>NESSIB, Nabil</au><au>BELLAGHA, Ibtissem</au><au>MAHER BEN GHACHEM</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Childhood soft tissue chondroma. Two cases report</atitle><jtitle>Tunisie Medicale</jtitle><addtitle>Tunis Med</addtitle><date>2011-04</date><risdate>2011</risdate><volume>89</volume><issue>4</issue><spage>379</spage><epage>382</epage><pages>379-382</pages><issn>0041-4131</issn><coden>TUMEAF</coden><abstract>Soft tissue chondroma is a rare benign tumour, which is generally seen in adult. It consists of islands of heterotopic cartilaginous tissue and most localised on the hands and the feet. The hypothesis that microtrauma is involved in the aetiology of this condition has yet to find any factual support.
To report two paediatric cases of soft tissue chondroma.
The first is a soft tissue chondroma of the posterior aspect of the left axilla in a 3-year-old boy. CT scans showed a spherical fatty density soft tissue mass without evident calcifications, attaching the infraspinous muscle. The second patient is a 9-year-old girl presented with a right auricular finger soft tissue chondroma. Radiographs showed several punctuated calcifications with adjacent bone scalloping. MRI revealed a lobulated soft tissue mass attaching the flexor tendons. The tumours were entirely removed. Histological examination showed cartilaginous tissue in both cases. At follow-up, the patients had good functions without evidence of recurrence.
Simple excision should suffice to treat soft tissue chondroma but care should be taken to make the excision complete if recurrence are to be avoided.</abstract><cop>Tunis</cop><pub>Société tunisienne des sciences médicales</pub><pmid>21484690</pmid><tpages>4</tpages></addata></record> |
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| ispartof | Tunisie Medicale, 2011-04, Vol.89 (4), p.379-382 |
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| language | eng ; fre |
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| source | MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
| subjects | Axilla - pathology Child Child, Preschool Chondroma - diagnostic imaging Chondroma - pathology Chondroma - surgery Female Fingers - pathology Generalites Humans Male Pathologie osteoarticulaire Radiography Sciences biologiques et medicales Sciences medicales Soft Tissue Neoplasms - diagnostic imaging Soft Tissue Neoplasms - pathology Soft Tissue Neoplasms - surgery Treatment Outcome Tumeurs du muscle strié et du squelette |
| title | Childhood soft tissue chondroma. Two cases report |
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