Literature DB >> 9471546

[Atypical and incomplete Kawasaki disease].

V Rossomando1, A Baracchini, G Chiaravalloti, N Assanta, G Buti, L Matteucci, M Ceccarelli.   

Abstract

Kawasaki Disease (KD) is an acute systemic vasculitic disorder of childhood of unknown etiology. Initially KD was thought to be a benign disease, but later on it became obvious that cardiac manifestations are present in about 25-30% of patients and lead to death in about 0.5-2% of them. An early diagnosis and treatment are important to avoid an unfavourable prognosis. In recent years, a number of publications described patients in which the diagnosis was delayed because they did not fulfil the required criteria of KD. These forms of KD are known as atypical or incomplete KD. The aim of this work is to describe two cases of atypical KD observed at the Department of Pediatrics, University of Pisa during the year 1992.

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Year:  1997        PMID: 9471546

Source DB:  PubMed          Journal:  Minerva Pediatr        ISSN: 0026-4946            Impact factor:   1.312


  2 in total

1.  Comparison of Laboratory Data between Children with Kawasaki Disease and COVID-19.

Authors:  Xiao-Ping Liu; Ying-Hsien Huang; Yuh-Chyn Tsai; Shih-Feng Liu; Ho-Chang Kuo
Journal:  Children (Basel)       Date:  2022-04-28

2.  A novel nomogram model for differentiating Kawasaki disease from sepsis.

Authors:  Xiao-Ping Liu; Yi-Shuang Huang; Ho-Chang Kuo; Han-Bing Xia; Wei-Dong Huang; Xin-Ling Lang; Chun-Yi Liu; Xi Liu
Journal:  Sci Rep       Date:  2020-08-13       Impact factor: 4.379

  2 in total

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