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10.1093/tropej/fmaa047

http://scihub22266oqcxt.onion/10.1093/tropej/fmaa047
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32756980!7454926!32756980
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suck abstract from ncbi


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pmid32756980      J+Trop+Pediatr 2021 ; 67 (3): ä
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  • Incomplete Kawasaki Disease as Presentation of COVID-19 Infection in an Infant: A Case Report #MMPMID32756980
  • Raut S; Roychowdhoury S; Bhakta S; Sarkar M; Nandi M
  • J Trop Pediatr 2021[Jul]; 67 (3): ä PMID32756980show ga
  • BACKGROUND: Recently a severe form of COVID-19 infection has been described in a cluster of children presenting as multisystem inflammatory condition. One of the important spectrum of this condition is incomplete Kawasaki disease (KD). CASE REPORT: A 5-month-old male child presented with high-spiking fever for 5 days with skin rash, bilateral non-purulent conjunctivitis and irritability. His C-reactive protein was markedly elevated (215.4 mg/l). Echocardiography revealed dilated left main coronary artery (3.0 mm, Z score +4.30) and left anterior descending artery (2.37 mm, Z score +3.76). Concomitantly Reverse Transcription- Polymerase Chain Reaction for COVID-19 was positive on fifth day sample. He was diagnosed as incomplete KD with COVID-19 infection and treated with intravenous immunoglobulin (IVIG) (2 g/kg), oral aspirin and azithromycin. Patient improved after 48 h and was discharged on oral aspirin. CONCLUSION: Incomplete KD may co-exist with COVID-19 infection in infant. Early institution of IVIG may lead to better outcome.
  • |*COVID-19[MESH]
  • |*Mucocutaneous Lymph Node Syndrome/complications/diagnosis/drug therapy[MESH]
  • |Child[MESH]
  • |Humans[MESH]
  • |Immunoglobulins, Intravenous/therapeutic use[MESH]
  • |Immunologic Factors[MESH]
  • |Infant[MESH]
  • |Male[MESH]


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