KAWASAKI SYNDROME
Summary Kawasaki syndrome is an acute multisystem inflammatory disease of young children first described by Tomasaku Kawasaki in the Japanese literature in 19671 He reported 50 cases of this entity under the rubric of acute febrile mucocutaneous lymph node syndrome, a designation that has more recen...
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Veröffentlicht in: | Australasian journal of dermatology 1990-08, Vol.31 (2), p.61-71 |
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container_title | Australasian journal of dermatology |
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creator | Esterly, Nancy B. Wortmann, Dorothy W. |
description | Summary
Kawasaki syndrome is an acute multisystem inflammatory disease of young children first described by Tomasaku Kawasaki in the Japanese literature in 19671 He reported 50 cases of this entity under the rubric of acute febrile mucocutaneous lymph node syndrome, a designation that has more recently been superseded by the eponym Kawasaki syndrome. The disorder was further delineated and brought to the attention of American pediatricians in 19742. Recognition of the syndrome followed rapidly, and Melish, Hicks and Larson published the first series of American cases from Hawaii in 19763. Subsequently, Kawasaki syndrome has been documented worldwide. Although the disorder is known to be a systemic vasculitis with predilection for the coronary arteries, the etiology has remained obscure despite intense investigative efforts. |
doi_str_mv | 10.1111/j.1440-0960.1990.tb00653.x |
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Kawasaki syndrome is an acute multisystem inflammatory disease of young children first described by Tomasaku Kawasaki in the Japanese literature in 19671 He reported 50 cases of this entity under the rubric of acute febrile mucocutaneous lymph node syndrome, a designation that has more recently been superseded by the eponym Kawasaki syndrome. The disorder was further delineated and brought to the attention of American pediatricians in 19742. Recognition of the syndrome followed rapidly, and Melish, Hicks and Larson published the first series of American cases from Hawaii in 19763. Subsequently, Kawasaki syndrome has been documented worldwide. Although the disorder is known to be a systemic vasculitis with predilection for the coronary arteries, the etiology has remained obscure despite intense investigative efforts.</description><identifier>ISSN: 0004-8380</identifier><identifier>EISSN: 1440-0960</identifier><identifier>DOI: 10.1111/j.1440-0960.1990.tb00653.x</identifier><identifier>PMID: 2095737</identifier><identifier>CODEN: AJDEBP</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Acute Disease ; Biological and medical sciences ; coronary arteries ; Dermatology ; Diagnosis, Differential ; epidemiology ; exanthem ; Female ; fever ; Humans ; Infant ; Kawasaki syndrome ; Male ; Medical sciences ; Mucocutaneous Lymph Node Syndrome - diagnosis ; Mucocutaneous Lymph Node Syndrome - therapy</subject><ispartof>Australasian journal of dermatology, 1990-08, Vol.31 (2), p.61-71</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2931-36660e765f58d3806e30eb1da33a7d43678e91c8f047ea2daafc394a05bc02b43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1440-0960.1990.tb00653.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1440-0960.1990.tb00653.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5438963$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2095737$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Esterly, Nancy B.</creatorcontrib><creatorcontrib>Wortmann, Dorothy W.</creatorcontrib><title>KAWASAKI SYNDROME</title><title>Australasian journal of dermatology</title><addtitle>Australas J Dermatol</addtitle><description>Summary
Kawasaki syndrome is an acute multisystem inflammatory disease of young children first described by Tomasaku Kawasaki in the Japanese literature in 19671 He reported 50 cases of this entity under the rubric of acute febrile mucocutaneous lymph node syndrome, a designation that has more recently been superseded by the eponym Kawasaki syndrome. The disorder was further delineated and brought to the attention of American pediatricians in 19742. Recognition of the syndrome followed rapidly, and Melish, Hicks and Larson published the first series of American cases from Hawaii in 19763. Subsequently, Kawasaki syndrome has been documented worldwide. Although the disorder is known to be a systemic vasculitis with predilection for the coronary arteries, the etiology has remained obscure despite intense investigative efforts.</description><subject>Acute Disease</subject><subject>Biological and medical sciences</subject><subject>coronary arteries</subject><subject>Dermatology</subject><subject>Diagnosis, Differential</subject><subject>epidemiology</subject><subject>exanthem</subject><subject>Female</subject><subject>fever</subject><subject>Humans</subject><subject>Infant</subject><subject>Kawasaki syndrome</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mucocutaneous Lymph Node Syndrome - diagnosis</subject><subject>Mucocutaneous Lymph Node Syndrome - therapy</subject><issn>0004-8380</issn><issn>1440-0960</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkF9PwjAUxRujQUQf_AAmxhjfNm-5bbea-DABAUEwolGfmm7rkuH44woRvr1bWHi3L016zq_33EPIFQWXFud26lLGwAEpigcpwV2FAIKjuzkg9b10SOoAwBwffTgmJ9ZOAShSzmuk1gTJPfTq5HwQfASTYNC_nHyN2q_j584pOUp0Zs1ZdTfI-2PnrdVzhuNuvxUMnagpkToohADjCZ5wPy4mCINgQhprRO3FDIXnG0kjPwHmGd2MtU4ilEwDDyNohgwb5Gb37zJf_KyNXalZaiOTZXpuFmurfEBGJcPCeLczRvnC2twkapmnM51vFQVV9qGmqlxalUursg9V9aE2BXxRTVmHMxPv0aqAQr-udG0jnSW5nkep3ds4Q1-KMsP9zvabZmb7jwAqeGoLWvDOjk_tymz2vM6_lShicPUx6qrPB3xhfrunPPwDIYmG3g</recordid><startdate>199008</startdate><enddate>199008</enddate><creator>Esterly, Nancy B.</creator><creator>Wortmann, Dorothy W.</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>199008</creationdate><title>KAWASAKI SYNDROME</title><author>Esterly, Nancy B. ; Wortmann, Dorothy W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2931-36660e765f58d3806e30eb1da33a7d43678e91c8f047ea2daafc394a05bc02b43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Acute Disease</topic><topic>Biological and medical sciences</topic><topic>coronary arteries</topic><topic>Dermatology</topic><topic>Diagnosis, Differential</topic><topic>epidemiology</topic><topic>exanthem</topic><topic>Female</topic><topic>fever</topic><topic>Humans</topic><topic>Infant</topic><topic>Kawasaki syndrome</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mucocutaneous Lymph Node Syndrome - diagnosis</topic><topic>Mucocutaneous Lymph Node Syndrome - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Esterly, Nancy B.</creatorcontrib><creatorcontrib>Wortmann, Dorothy W.</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>Australasian journal of dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Esterly, Nancy B.</au><au>Wortmann, Dorothy W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>KAWASAKI SYNDROME</atitle><jtitle>Australasian journal of dermatology</jtitle><addtitle>Australas J Dermatol</addtitle><date>1990-08</date><risdate>1990</risdate><volume>31</volume><issue>2</issue><spage>61</spage><epage>71</epage><pages>61-71</pages><issn>0004-8380</issn><eissn>1440-0960</eissn><coden>AJDEBP</coden><abstract>Summary
Kawasaki syndrome is an acute multisystem inflammatory disease of young children first described by Tomasaku Kawasaki in the Japanese literature in 19671 He reported 50 cases of this entity under the rubric of acute febrile mucocutaneous lymph node syndrome, a designation that has more recently been superseded by the eponym Kawasaki syndrome. The disorder was further delineated and brought to the attention of American pediatricians in 19742. Recognition of the syndrome followed rapidly, and Melish, Hicks and Larson published the first series of American cases from Hawaii in 19763. Subsequently, Kawasaki syndrome has been documented worldwide. Although the disorder is known to be a systemic vasculitis with predilection for the coronary arteries, the etiology has remained obscure despite intense investigative efforts.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>2095737</pmid><doi>10.1111/j.1440-0960.1990.tb00653.x</doi><tpages>11</tpages></addata></record> |
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source | MEDLINE; Wiley Blackwell Single Titles |
subjects | Acute Disease Biological and medical sciences coronary arteries Dermatology Diagnosis, Differential epidemiology exanthem Female fever Humans Infant Kawasaki syndrome Male Medical sciences Mucocutaneous Lymph Node Syndrome - diagnosis Mucocutaneous Lymph Node Syndrome - therapy |
title | KAWASAKI SYNDROME |
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