Large Congenital Melanocytic Nevi and the Risk for Development of Malignant Melanoma and Neurocutaneous Melanocytosis
To determine the risk for developing malignant melanoma and neurocutaneous melanocytosis (NCM) in patients with large congenital melanocytic nevi. Follow-up data suitable for calculations were available on 160 patients in the New York University Registry of Large Congenital Melanocytic Nevi who had...
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Veröffentlicht in: | Pediatrics (Evanston) 2000-10, Vol.106 (4), p.736-741 |
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description | To determine the risk for developing malignant melanoma and neurocutaneous melanocytosis (NCM) in patients with large congenital melanocytic nevi.
Follow-up data suitable for calculations were available on 160 patients in the New York University Registry of Large Congenital Melanocytic Nevi who had been free of known melanomas or NCM when entered into the Registry. The cumulative 5-year life-table risks for developing melanoma and NCM were calculated. The relative risk for developing melanoma, using a control general population reference group, was determined.
The 160 patients (median age at entry: 14 months) were followed prospectively for an average of 5.5 years. Three extracutaneous melanomas developed: 2 were in the central nervous system (CNS) and 1 was retroperitoneal. The 5-year cumulative life-table risk for developing melanoma was 2.3% (95% confidence interval [CI]:.8-6.6) and the relative risk was 101 (95% CI: 21-296). No melanoma occurred within a large congenital melanocytic nevus. Four patients developed manifest NCM, 2 with CNS melanomas. The 5-year cumulative life-table risk for developing NCM was 2.5% (95% CI:.8-7.2). Ten patients were excluded from the calculations because of preexisting disease on entry into the Registry: 5 with manifest NCM and 5 with melanomas (3 in large congenital melanocytic nevi, 1 in nonnevus skin, and 1 unknown primary).
Patients with large congenital melanocytic nevi are at increased risk for developing melanomas. There is also a significant increased risk for developing NCM. The high incidence of CNS involvement may influence decisions concerning treatment of the large congenital melanocytic nevi. |
doi_str_mv | 10.1542/peds.106.4.736 |
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Follow-up data suitable for calculations were available on 160 patients in the New York University Registry of Large Congenital Melanocytic Nevi who had been free of known melanomas or NCM when entered into the Registry. The cumulative 5-year life-table risks for developing melanoma and NCM were calculated. The relative risk for developing melanoma, using a control general population reference group, was determined.
The 160 patients (median age at entry: 14 months) were followed prospectively for an average of 5.5 years. Three extracutaneous melanomas developed: 2 were in the central nervous system (CNS) and 1 was retroperitoneal. The 5-year cumulative life-table risk for developing melanoma was 2.3% (95% confidence interval [CI]:.8-6.6) and the relative risk was 101 (95% CI: 21-296). No melanoma occurred within a large congenital melanocytic nevus. Four patients developed manifest NCM, 2 with CNS melanomas. The 5-year cumulative life-table risk for developing NCM was 2.5% (95% CI:.8-7.2). Ten patients were excluded from the calculations because of preexisting disease on entry into the Registry: 5 with manifest NCM and 5 with melanomas (3 in large congenital melanocytic nevi, 1 in nonnevus skin, and 1 unknown primary).
Patients with large congenital melanocytic nevi are at increased risk for developing melanomas. There is also a significant increased risk for developing NCM. The high incidence of CNS involvement may influence decisions concerning treatment of the large congenital melanocytic nevi.</description><identifier>ISSN: 0031-4005</identifier><identifier>EISSN: 1098-4275</identifier><identifier>DOI: 10.1542/peds.106.4.736</identifier><identifier>PMID: 11015516</identifier><identifier>CODEN: PEDIAU</identifier><language>eng</language><publisher>Elk Grove Village, IL: Am Acad Pediatrics</publisher><subject>Adolescent ; Adult ; Biological and medical sciences ; Cancer ; Child ; Child, Preschool ; Dermatology ; Female ; Follow-Up Studies ; Health aspects ; Health risk assessment ; Humans ; Infant ; Life Tables ; Male ; Medical sciences ; Melanoma ; Melanoma - epidemiology ; Melanoma - etiology ; Melanosis - epidemiology ; Melanosis - etiology ; Melanosis - mortality ; Middle Aged ; Mole (Dermatology) ; Nervous system ; Neurocutaneous Syndromes - epidemiology ; Neurocutaneous Syndromes - etiology ; Neurocutaneous Syndromes - mortality ; Nevus ; Nevus, Pigmented - complications ; Nevus, Pigmented - congenital ; New York - epidemiology ; Pediatrics ; Registries ; Risk ; Risk factors ; Tumors of the skin and soft tissue. Premalignant lesions</subject><ispartof>Pediatrics (Evanston), 2000-10, Vol.106 (4), p.736-741</ispartof><rights>2000 INIST-CNRS</rights><rights>COPYRIGHT 2000 American Academy of Pediatrics</rights><rights>COPYRIGHT 2000 American Academy of Pediatrics</rights><rights>Copyright American Academy of Pediatrics Oct 2000</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c560t-7a3bc38dd4b6245f2d7cf8cfb7b61babc0e827979c83ca34adbd47c524b9e2273</citedby><cites>FETCH-LOGICAL-c560t-7a3bc38dd4b6245f2d7cf8cfb7b61babc0e827979c83ca34adbd47c524b9e2273</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=1529452$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11015516$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bittencourt, Flavia V</creatorcontrib><creatorcontrib>Marghoob, Ashfaq A</creatorcontrib><creatorcontrib>Kopf, Alfred W</creatorcontrib><creatorcontrib>Koenig, Karen L</creatorcontrib><creatorcontrib>Bart, Robert S</creatorcontrib><title>Large Congenital Melanocytic Nevi and the Risk for Development of Malignant Melanoma and Neurocutaneous Melanocytosis</title><title>Pediatrics (Evanston)</title><addtitle>Pediatrics</addtitle><description>To determine the risk for developing malignant melanoma and neurocutaneous melanocytosis (NCM) in patients with large congenital melanocytic nevi.
Follow-up data suitable for calculations were available on 160 patients in the New York University Registry of Large Congenital Melanocytic Nevi who had been free of known melanomas or NCM when entered into the Registry. The cumulative 5-year life-table risks for developing melanoma and NCM were calculated. The relative risk for developing melanoma, using a control general population reference group, was determined.
The 160 patients (median age at entry: 14 months) were followed prospectively for an average of 5.5 years. Three extracutaneous melanomas developed: 2 were in the central nervous system (CNS) and 1 was retroperitoneal. The 5-year cumulative life-table risk for developing melanoma was 2.3% (95% confidence interval [CI]:.8-6.6) and the relative risk was 101 (95% CI: 21-296). No melanoma occurred within a large congenital melanocytic nevus. Four patients developed manifest NCM, 2 with CNS melanomas. The 5-year cumulative life-table risk for developing NCM was 2.5% (95% CI:.8-7.2). Ten patients were excluded from the calculations because of preexisting disease on entry into the Registry: 5 with manifest NCM and 5 with melanomas (3 in large congenital melanocytic nevi, 1 in nonnevus skin, and 1 unknown primary).
Patients with large congenital melanocytic nevi are at increased risk for developing melanomas. There is also a significant increased risk for developing NCM. The high incidence of CNS involvement may influence decisions concerning treatment of the large congenital melanocytic nevi.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Cancer</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Dermatology</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Health aspects</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Infant</subject><subject>Life Tables</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Melanoma</subject><subject>Melanoma - epidemiology</subject><subject>Melanoma - etiology</subject><subject>Melanosis - epidemiology</subject><subject>Melanosis - etiology</subject><subject>Melanosis - mortality</subject><subject>Middle Aged</subject><subject>Mole (Dermatology)</subject><subject>Nervous system</subject><subject>Neurocutaneous Syndromes - epidemiology</subject><subject>Neurocutaneous Syndromes - etiology</subject><subject>Neurocutaneous Syndromes - mortality</subject><subject>Nevus</subject><subject>Nevus, Pigmented - complications</subject><subject>Nevus, Pigmented - congenital</subject><subject>New York - epidemiology</subject><subject>Pediatrics</subject><subject>Registries</subject><subject>Risk</subject><subject>Risk factors</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><issn>0031-4005</issn><issn>1098-4275</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0s1v0zAUAPAIgVgZXDmiCCHEYSm2Y8fJcSowkLpNQnC2HOcl9XDsYjuD_fe4pFIpqn3wh37Pz3p6WfYSoyVmlLzfQheWGFVLuuRl9ShbYNTUBSWcPc4WCJW4oAixs-xZCHcIIco4eZqdYYwwY7haZNNa-gHylbMDWB2lya_BSOvUQ9Qqv4F7nUvb5XED-VcdfuS98_kHuAfjtiPYmLs-v5ZGD1amwxw6yr8hNzB5p6YoLbgpHJ51QYfn2ZNemgAv9ut59v3Tx2-rz8X69urL6nJdKFahWHBZtqqsu462FaGsJx1Xfa36lrcVbmWrENSEN7xRdalkSWXXdpQrRmjbACG8PM_ezu9uvfs5QYhi1EGBMfOnBCclqlBVJvj6P3jnJm_T3wQhNcWYIprQxYwGaUBo27vopUp1Ay-Ns9DrdH1ZpcFQ0yRenOBpdjBqdcq_O_KJRPgdBzmFIOqr9RG9OEWVMwYGEKmGq9sjvpy58i4ED73Yej1K_yAwErs2Ers2SodKUJHaKAW82pdjakfoDnzfNwm82QMZlDS9l1bpcHCMNJSRQ-KNHja_tIddIi2j1yr8sz0k_gPsOeAn</recordid><startdate>20001001</startdate><enddate>20001001</enddate><creator>Bittencourt, Flavia V</creator><creator>Marghoob, Ashfaq A</creator><creator>Kopf, Alfred W</creator><creator>Koenig, Karen L</creator><creator>Bart, Robert S</creator><general>Am Acad Pediatrics</general><general>American Academy of Pediatrics</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>8GL</scope><scope>7TS</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>U9A</scope><scope>7X8</scope></search><sort><creationdate>20001001</creationdate><title>Large Congenital Melanocytic Nevi and the Risk for Development of Malignant Melanoma and Neurocutaneous Melanocytosis</title><author>Bittencourt, Flavia V ; Marghoob, Ashfaq A ; Kopf, Alfred W ; Koenig, Karen L ; Bart, Robert S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c560t-7a3bc38dd4b6245f2d7cf8cfb7b61babc0e827979c83ca34adbd47c524b9e2273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Cancer</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Dermatology</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Health aspects</topic><topic>Health risk assessment</topic><topic>Humans</topic><topic>Infant</topic><topic>Life Tables</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Melanoma</topic><topic>Melanoma - epidemiology</topic><topic>Melanoma - etiology</topic><topic>Melanosis - epidemiology</topic><topic>Melanosis - etiology</topic><topic>Melanosis - mortality</topic><topic>Middle Aged</topic><topic>Mole (Dermatology)</topic><topic>Nervous system</topic><topic>Neurocutaneous Syndromes - epidemiology</topic><topic>Neurocutaneous Syndromes - etiology</topic><topic>Neurocutaneous Syndromes - mortality</topic><topic>Nevus</topic><topic>Nevus, Pigmented - complications</topic><topic>Nevus, Pigmented - congenital</topic><topic>New York - epidemiology</topic><topic>Pediatrics</topic><topic>Registries</topic><topic>Risk</topic><topic>Risk factors</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bittencourt, Flavia V</creatorcontrib><creatorcontrib>Marghoob, Ashfaq A</creatorcontrib><creatorcontrib>Kopf, Alfred W</creatorcontrib><creatorcontrib>Koenig, Karen L</creatorcontrib><creatorcontrib>Bart, Robert S</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>Gale In Context: High School</collection><collection>Physical Education Index</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatrics (Evanston)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bittencourt, Flavia V</au><au>Marghoob, Ashfaq A</au><au>Kopf, Alfred W</au><au>Koenig, Karen L</au><au>Bart, Robert S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Large Congenital Melanocytic Nevi and the Risk for Development of Malignant Melanoma and Neurocutaneous Melanocytosis</atitle><jtitle>Pediatrics (Evanston)</jtitle><addtitle>Pediatrics</addtitle><date>2000-10-01</date><risdate>2000</risdate><volume>106</volume><issue>4</issue><spage>736</spage><epage>741</epage><pages>736-741</pages><issn>0031-4005</issn><eissn>1098-4275</eissn><coden>PEDIAU</coden><abstract>To determine the risk for developing malignant melanoma and neurocutaneous melanocytosis (NCM) in patients with large congenital melanocytic nevi.
Follow-up data suitable for calculations were available on 160 patients in the New York University Registry of Large Congenital Melanocytic Nevi who had been free of known melanomas or NCM when entered into the Registry. The cumulative 5-year life-table risks for developing melanoma and NCM were calculated. The relative risk for developing melanoma, using a control general population reference group, was determined.
The 160 patients (median age at entry: 14 months) were followed prospectively for an average of 5.5 years. Three extracutaneous melanomas developed: 2 were in the central nervous system (CNS) and 1 was retroperitoneal. The 5-year cumulative life-table risk for developing melanoma was 2.3% (95% confidence interval [CI]:.8-6.6) and the relative risk was 101 (95% CI: 21-296). No melanoma occurred within a large congenital melanocytic nevus. Four patients developed manifest NCM, 2 with CNS melanomas. The 5-year cumulative life-table risk for developing NCM was 2.5% (95% CI:.8-7.2). Ten patients were excluded from the calculations because of preexisting disease on entry into the Registry: 5 with manifest NCM and 5 with melanomas (3 in large congenital melanocytic nevi, 1 in nonnevus skin, and 1 unknown primary).
Patients with large congenital melanocytic nevi are at increased risk for developing melanomas. There is also a significant increased risk for developing NCM. The high incidence of CNS involvement may influence decisions concerning treatment of the large congenital melanocytic nevi.</abstract><cop>Elk Grove Village, IL</cop><pub>Am Acad Pediatrics</pub><pmid>11015516</pmid><doi>10.1542/peds.106.4.736</doi><tpages>6</tpages></addata></record> |
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subjects | Adolescent Adult Biological and medical sciences Cancer Child Child, Preschool Dermatology Female Follow-Up Studies Health aspects Health risk assessment Humans Infant Life Tables Male Medical sciences Melanoma Melanoma - epidemiology Melanoma - etiology Melanosis - epidemiology Melanosis - etiology Melanosis - mortality Middle Aged Mole (Dermatology) Nervous system Neurocutaneous Syndromes - epidemiology Neurocutaneous Syndromes - etiology Neurocutaneous Syndromes - mortality Nevus Nevus, Pigmented - complications Nevus, Pigmented - congenital New York - epidemiology Pediatrics Registries Risk Risk factors Tumors of the skin and soft tissue. Premalignant lesions |
title | Large Congenital Melanocytic Nevi and the Risk for Development of Malignant Melanoma and Neurocutaneous Melanocytosis |
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