Literature DB >> 17263

Infantile polyarteritis and Kawasaki disease.

A D Smith.   

Abstract

Polyarteritis in infancy is very rare, difficult to diagnose and invariably fatal. A 6-month-old girl who presented with a prolonged unexplained fever and was subsequently demonstrated at post-mortem examination to have polyarteritis is described. The combination of polyarterits with some unusual presenting features suggests that the case described is one of the Mucocutaneous Lymph Node Syndrome (M.L.N.S.) or Kawasaki Disease. Polyarteritis and Kawasaki Disease are discussed with reference to the case described.

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Mesh:

Year:  1977        PMID: 17263     DOI: 10.1111/j.1651-2227.1977.tb07911.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


  2 in total

1.  Mucocutaneous lymph node syndrome with necrotic pharyngitis.

Authors:  L Brion; M Courtoy; D Bachelart; H Szliwowski; M Dickstein; M Heenen; M Tondeur
Journal:  Eur J Pediatr       Date:  1980-10       Impact factor: 3.183

2.  [Case report: death of a 2-year-old girl with postmortem diagnosis of a rare coronary artery vasculitis typical for Kawasaki syndrome].

Authors:  K Kanngießer; N Kono; J-T Suhren; M Klintschar
Journal:  Rechtsmedizin (Berl)       Date:  2021-04-23       Impact factor: 0.517

  2 in total

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