Congenital vascular lesions: Clinical application of a new classification
Two hundred and ninety-seven patients with 375 pediatric vascular lesions were followed from 1967 to 1981. By history and physical examination, 96% of childhood vascular lesions can be classified as hemangiomas or malformations. Hemangiomas are often not present at birth (40%), but make their appear...
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Veröffentlicht in: | Journal of pediatric surgery 1983-12, Vol.18 (6), p.894-900 |
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creator | Collins Finn, Mary Glowacki, Julie Mulliken, John B. |
description | Two hundred and ninety-seven patients with 375 pediatric vascular lesions were followed from 1967 to 1981. By history and physical examination, 96% of childhood vascular lesions can be classified as hemangiomas or malformations. Hemangiomas are often not present at birth (40%), but make their appearance during the first month. A proliferative phase, lasting an average of 3 months, is followed by a slow, but eventually complete involution. A “perfect” cosmetic result is more likely when involution is complete before age 6. Malformations are always present at birth, their growth is communsurate with the patient's, and they never involute. Analysis of clinical characteristics fails to identify a subgroup of hemangiomas destined for early involution. |
doi_str_mv | 10.1016/S0022-3468(83)80043-8 |
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By history and physical examination, 96% of childhood vascular lesions can be classified as hemangiomas or malformations. Hemangiomas are often not present at birth (40%), but make their appearance during the first month. A proliferative phase, lasting an average of 3 months, is followed by a slow, but eventually complete involution. A “perfect” cosmetic result is more likely when involution is complete before age 6. Malformations are always present at birth, their growth is communsurate with the patient's, and they never involute. Analysis of clinical characteristics fails to identify a subgroup of hemangiomas destined for early involution.</description><identifier>ISSN: 0022-3468</identifier><identifier>EISSN: 1531-5037</identifier><identifier>DOI: 10.1016/S0022-3468(83)80043-8</identifier><identifier>PMID: 6663421</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Arteriovenous Malformations - classification ; Child ; Child, Preschool ; Female ; Hemangioma ; Hemangioma - classification ; Hemangioma - congenital ; Humans ; Infant ; Infant, Newborn ; lymphangioma ; Lymphangioma - classification ; Lymphangioma - congenital ; Male ; Physical Examination ; vascular malformation</subject><ispartof>Journal of pediatric surgery, 1983-12, Vol.18 (6), p.894-900</ispartof><rights>1983 Grune & Stratton, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c360t-ed61e83fe1dc2da3b021fc2310e573e256bcea2c663134beb395993941db1f4d3</citedby><cites>FETCH-LOGICAL-c360t-ed61e83fe1dc2da3b021fc2310e573e256bcea2c663134beb395993941db1f4d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022346883800438$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6663421$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Collins Finn, Mary</creatorcontrib><creatorcontrib>Glowacki, Julie</creatorcontrib><creatorcontrib>Mulliken, John B.</creatorcontrib><title>Congenital vascular lesions: Clinical application of a new classification</title><title>Journal of pediatric surgery</title><addtitle>J Pediatr Surg</addtitle><description>Two hundred and ninety-seven patients with 375 pediatric vascular lesions were followed from 1967 to 1981. By history and physical examination, 96% of childhood vascular lesions can be classified as hemangiomas or malformations. Hemangiomas are often not present at birth (40%), but make their appearance during the first month. A proliferative phase, lasting an average of 3 months, is followed by a slow, but eventually complete involution. A “perfect” cosmetic result is more likely when involution is complete before age 6. Malformations are always present at birth, their growth is communsurate with the patient's, and they never involute. Analysis of clinical characteristics fails to identify a subgroup of hemangiomas destined for early involution.</description><subject>Adolescent</subject><subject>Arteriovenous Malformations - classification</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Female</subject><subject>Hemangioma</subject><subject>Hemangioma - classification</subject><subject>Hemangioma - congenital</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>lymphangioma</subject><subject>Lymphangioma - classification</subject><subject>Lymphangioma - congenital</subject><subject>Male</subject><subject>Physical Examination</subject><subject>vascular malformation</subject><issn>0022-3468</issn><issn>1531-5037</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1OwzAQhC0EKqXwCJVyQnAI2NkkdbggFPFTqRIH4Gw59gYZuUmwkyLeHreNeuXk1cysd_cjZM7oDaMsv32jNEliSHN-xeGaU5pCzI_IlGXA4ozC4phMD5FTcub9F6VBpmxCJnmeQ5qwKVmWbfOJjemljTbSq8FKF1n0pm38XVRa0xgVLNl1NhR9kKO2jmTU4E-krPTe1KN-Tk5qaT1ejO-MfDw9vpcv8er1eVk-rGIFOe1j1DlDDjUyrRItoaIJq1UCjGK2AEyyvFIoExUWZJBWWEGRFQUUKdMVq1MNM3K5_7dz7feAvhdr4xVaKxtsBy845RnlCwjBbB9UrvXeYS06Z9bS_QpGxRah2CEUWz6Cg9ghDMWMzMcBQ7VGfegamQX_fu9juHJj0AmvDDYKtXGoeqFb88-EP_INgMc</recordid><startdate>198312</startdate><enddate>198312</enddate><creator>Collins Finn, Mary</creator><creator>Glowacki, Julie</creator><creator>Mulliken, John B.</creator><general>Elsevier Inc</general><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>198312</creationdate><title>Congenital vascular lesions: Clinical application of a new classification</title><author>Collins Finn, Mary ; Glowacki, Julie ; Mulliken, John B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c360t-ed61e83fe1dc2da3b021fc2310e573e256bcea2c663134beb395993941db1f4d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1983</creationdate><topic>Adolescent</topic><topic>Arteriovenous Malformations - classification</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Female</topic><topic>Hemangioma</topic><topic>Hemangioma - classification</topic><topic>Hemangioma - congenital</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>lymphangioma</topic><topic>Lymphangioma - classification</topic><topic>Lymphangioma - congenital</topic><topic>Male</topic><topic>Physical Examination</topic><topic>vascular malformation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Collins Finn, Mary</creatorcontrib><creatorcontrib>Glowacki, Julie</creatorcontrib><creatorcontrib>Mulliken, John B.</creatorcontrib><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>Journal of pediatric surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Collins Finn, Mary</au><au>Glowacki, Julie</au><au>Mulliken, John B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Congenital vascular lesions: Clinical application of a new classification</atitle><jtitle>Journal of pediatric surgery</jtitle><addtitle>J Pediatr Surg</addtitle><date>1983-12</date><risdate>1983</risdate><volume>18</volume><issue>6</issue><spage>894</spage><epage>900</epage><pages>894-900</pages><issn>0022-3468</issn><eissn>1531-5037</eissn><abstract>Two hundred and ninety-seven patients with 375 pediatric vascular lesions were followed from 1967 to 1981. By history and physical examination, 96% of childhood vascular lesions can be classified as hemangiomas or malformations. Hemangiomas are often not present at birth (40%), but make their appearance during the first month. A proliferative phase, lasting an average of 3 months, is followed by a slow, but eventually complete involution. A “perfect” cosmetic result is more likely when involution is complete before age 6. Malformations are always present at birth, their growth is communsurate with the patient's, and they never involute. Analysis of clinical characteristics fails to identify a subgroup of hemangiomas destined for early involution.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>6663421</pmid><doi>10.1016/S0022-3468(83)80043-8</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Arteriovenous Malformations - classification Child Child, Preschool Female Hemangioma Hemangioma - classification Hemangioma - congenital Humans Infant Infant, Newborn lymphangioma Lymphangioma - classification Lymphangioma - congenital Male Physical Examination vascular malformation |
title | Congenital vascular lesions: Clinical application of a new classification |
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