Ollier's disease associated with ovarian juvenile granulosa cell tumor
A six‐year‐old girl had Ollier's disease (OD) associated with juvenile granulosa cell tumor (JGCT). The clinical manifestations were right hemicorporal deformity due to multiple skeletal enchondromas and precocious pseudopuberty. After the removal of a Stage Iai JGCT, hormonal symptoms disappea...
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| Veröffentlicht in: | Cancer 1988-07, Vol.62 (1), p.222-225 |
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| creator | Velasco‐Oses, Angel Alonso‐Alvaro, Angel Blanco‐Pozo, Agustin Nogales, Francisco F. |
| description | A six‐year‐old girl had Ollier's disease (OD) associated with juvenile granulosa cell tumor (JGCT). The clinical manifestations were right hemicorporal deformity due to multiple skeletal enchondromas and precocious pseudopuberty. After the removal of a Stage Iai JGCT, hormonal symptoms disappeared. Neither the ovarian tumor recurred nor the enchondromas underwent sarcomatous change after a follow‐up period of 7 years. A review of the literature showed five previous cases, three associated with OD and two with Mafucci's syndrome (MS). In these cases, patients were young and the ovarian tumors were homolateral to the hemicorporal side involved by enchondromatosis. Data provided from these cases emphasize the notion of a generalized mesodermal dysplasia. JGCT behave in association with the OD in its usual fashion of hormonal production and low‐degree aggressiveness. |
| doi_str_mv | 10.1002/1097-0142(19880701)62:1<222::AID-CNCR2820620134>3.0.CO;2-W |
| format | Article |
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The clinical manifestations were right hemicorporal deformity due to multiple skeletal enchondromas and precocious pseudopuberty. After the removal of a Stage Iai JGCT, hormonal symptoms disappeared. Neither the ovarian tumor recurred nor the enchondromas underwent sarcomatous change after a follow‐up period of 7 years. A review of the literature showed five previous cases, three associated with OD and two with Mafucci's syndrome (MS). In these cases, patients were young and the ovarian tumors were homolateral to the hemicorporal side involved by enchondromatosis. Data provided from these cases emphasize the notion of a generalized mesodermal dysplasia. JGCT behave in association with the OD in its usual fashion of hormonal production and low‐degree aggressiveness.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/1097-0142(19880701)62:1<222::AID-CNCR2820620134>3.0.CO;2-W</identifier><identifier>PMID: 3383118</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; Diseases of the osteoarticular system ; Enchondromatosis - complications ; Enchondromatosis - diagnostic imaging ; Female ; Female genital diseases ; Granulosa Cell Tumor - complications ; Gynecology. Andrology. Obstetrics ; Humans ; Malformations and congenital and or hereditary diseases involving bones. Joint deformations ; Medical sciences ; Osteochondrodysplasias - complications ; Ovarian Neoplasms - complications ; Ovarian Neoplasms - pathology ; Radiography ; Tumors</subject><ispartof>Cancer, 1988-07, Vol.62 (1), p.222-225</ispartof><rights>Copyright © 1988 American Cancer Society</rights><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4954-6684d0a8595e85c6d94010db4acb03c75c33e99308b3b153663360c351c198883</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7372747$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3383118$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Velasco‐Oses, Angel</creatorcontrib><creatorcontrib>Alonso‐Alvaro, Angel</creatorcontrib><creatorcontrib>Blanco‐Pozo, Agustin</creatorcontrib><creatorcontrib>Nogales, Francisco F.</creatorcontrib><title>Ollier's disease associated with ovarian juvenile granulosa cell tumor</title><title>Cancer</title><addtitle>Cancer</addtitle><description>A six‐year‐old girl had Ollier's disease (OD) associated with juvenile granulosa cell tumor (JGCT). The clinical manifestations were right hemicorporal deformity due to multiple skeletal enchondromas and precocious pseudopuberty. After the removal of a Stage Iai JGCT, hormonal symptoms disappeared. Neither the ovarian tumor recurred nor the enchondromas underwent sarcomatous change after a follow‐up period of 7 years. A review of the literature showed five previous cases, three associated with OD and two with Mafucci's syndrome (MS). In these cases, patients were young and the ovarian tumors were homolateral to the hemicorporal side involved by enchondromatosis. Data provided from these cases emphasize the notion of a generalized mesodermal dysplasia. JGCT behave in association with the OD in its usual fashion of hormonal production and low‐degree aggressiveness.</description><subject>Biological and medical sciences</subject><subject>Diseases of the osteoarticular system</subject><subject>Enchondromatosis - complications</subject><subject>Enchondromatosis - diagnostic imaging</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>Granulosa Cell Tumor - complications</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Malformations and congenital and or hereditary diseases involving bones. Joint deformations</subject><subject>Medical sciences</subject><subject>Osteochondrodysplasias - complications</subject><subject>Ovarian Neoplasms - complications</subject><subject>Ovarian Neoplasms - pathology</subject><subject>Radiography</subject><subject>Tumors</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkF1rFDEYhYNY6rb6E4S5EK0Xs77Jm6_ZSqGOrRaKC6JUvAmZTFZTZnfaZKel_94Muy7oheBVEs6Tw-Eh5B2FKQVgbyhUqgTK2RGttAYF9LVkM_qWMTabnV68L-tP9WemGUgGFPkJTmFaz49ZefWITHafH5MJAOhScPz2hBykdJ2figncJ_uIGinVE3I-77rg46tUtCF5m3xhU-pdsGvfFvdh_bPo72wMdlVcD3d-FTpf_Ih2NXR9soXzXVesh2Ufn5K9he2Sf7Y9D8nX87Mv9cfycv7hoj69LB2vBC-l1LwFq0UlvBZOthUHCm3DrWsAnRIO0VcVgm6woQKlRJTgUFA3mtB4SF5uem9ifzv4tDbLkMYZduX7IRmlmdAgRAa_b0AX-5SiX5ibGJY2PhgKZpRsRk9m9GR-SzYy302WbEyWbP6UbNCAqeeGmatc_ny7YmiWvt1Vb63m_MU2t8nZbpGFuZB2mELFFFcZ8xvsPmt9-K-B_9z3V4K_AFRdpJU</recordid><startdate>19880701</startdate><enddate>19880701</enddate><creator>Velasco‐Oses, Angel</creator><creator>Alonso‐Alvaro, Angel</creator><creator>Blanco‐Pozo, Agustin</creator><creator>Nogales, Francisco F.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</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>7X8</scope></search><sort><creationdate>19880701</creationdate><title>Ollier's disease associated with ovarian juvenile granulosa cell tumor</title><author>Velasco‐Oses, Angel ; Alonso‐Alvaro, Angel ; Blanco‐Pozo, Agustin ; Nogales, Francisco F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4954-6684d0a8595e85c6d94010db4acb03c75c33e99308b3b153663360c351c198883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Biological and medical sciences</topic><topic>Diseases of the osteoarticular system</topic><topic>Enchondromatosis - complications</topic><topic>Enchondromatosis - diagnostic imaging</topic><topic>Female</topic><topic>Female genital diseases</topic><topic>Granulosa Cell Tumor - complications</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Malformations and congenital and or hereditary diseases involving bones. Joint deformations</topic><topic>Medical sciences</topic><topic>Osteochondrodysplasias - complications</topic><topic>Ovarian Neoplasms - complications</topic><topic>Ovarian Neoplasms - pathology</topic><topic>Radiography</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Velasco‐Oses, Angel</creatorcontrib><creatorcontrib>Alonso‐Alvaro, Angel</creatorcontrib><creatorcontrib>Blanco‐Pozo, Agustin</creatorcontrib><creatorcontrib>Nogales, Francisco F.</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>MEDLINE - Academic</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Velasco‐Oses, Angel</au><au>Alonso‐Alvaro, Angel</au><au>Blanco‐Pozo, Agustin</au><au>Nogales, Francisco F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ollier's disease associated with ovarian juvenile granulosa cell tumor</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>1988-07-01</date><risdate>1988</risdate><volume>62</volume><issue>1</issue><spage>222</spage><epage>225</epage><pages>222-225</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>A six‐year‐old girl had Ollier's disease (OD) associated with juvenile granulosa cell tumor (JGCT). The clinical manifestations were right hemicorporal deformity due to multiple skeletal enchondromas and precocious pseudopuberty. After the removal of a Stage Iai JGCT, hormonal symptoms disappeared. Neither the ovarian tumor recurred nor the enchondromas underwent sarcomatous change after a follow‐up period of 7 years. A review of the literature showed five previous cases, three associated with OD and two with Mafucci's syndrome (MS). In these cases, patients were young and the ovarian tumors were homolateral to the hemicorporal side involved by enchondromatosis. Data provided from these cases emphasize the notion of a generalized mesodermal dysplasia. JGCT behave in association with the OD in its usual fashion of hormonal production and low‐degree aggressiveness.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>3383118</pmid><doi>10.1002/1097-0142(19880701)62:1<222::AID-CNCR2820620134>3.0.CO;2-W</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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| subjects | Biological and medical sciences Diseases of the osteoarticular system Enchondromatosis - complications Enchondromatosis - diagnostic imaging Female Female genital diseases Granulosa Cell Tumor - complications Gynecology. Andrology. Obstetrics Humans Malformations and congenital and or hereditary diseases involving bones. Joint deformations Medical sciences Osteochondrodysplasias - complications Ovarian Neoplasms - complications Ovarian Neoplasms - pathology Radiography Tumors |
| title | Ollier's disease associated with ovarian juvenile granulosa cell tumor |
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