Giant coronary arterial aneurysm in atypical Kawasaki disease

2009 ◽  
Vol 19 (4) ◽  
pp. 395-396
Author(s):  
Rebeca Sarrat Torres ◽  
Pedro Betrián Blasco ◽  
María Dolores García de la Calzada
2016 ◽  
Vol 27 (2) ◽  
pp. 375-376 ◽  
Author(s):  
Niall Johnston ◽  
David Coleman ◽  
Colin J. McMahon

AbstractWe describe the case of an 8-week-old infant with late presentation of severe refractory atypical Kawasaki disease. In addition to developing giant coronary arterial aneurysms and coronary thrombosis, she formed extensive bilateral arterial aneurysms throughout her systemic circulation.


2015 ◽  
Vol 2 ◽  
pp. 2333794X1559964 ◽  
Author(s):  
Elis Yuexian Lee ◽  
Jean Yin Oh ◽  
Chia Yin Chong ◽  
Jonathan Tze Liang Choo ◽  
Arjandas Mahadev ◽  
...  

2018 ◽  
pp. bcr-2017-221456 ◽  
Author(s):  
Nichkamol Lertamornkitti ◽  
Anchalee Wangjirapan

1999 ◽  
Vol 83 (1) ◽  
pp. 48-51 ◽  
Author(s):  
Nagib S Dahdah ◽  
Anne Fournier ◽  
Edgar Jaeggi ◽  
Nicolaas H van Doesburg ◽  
Raymond Lambert ◽  
...  

2020 ◽  
Vol 4 (2) ◽  
pp. 142-145 ◽  
Author(s):  
LCDR William Bylund ◽  
Gregory Zarow ◽  
LCDR Daphne Morrison Ponce

Kawasaki disease (KD) is a rare vasculitis of childhood that is critical to recognize and treat due to associated morbidity and mortality. A six-year-old male presented to our emergency department (ED) afebrile but with reported recent fevers. Exam revealed jaundice and erythematous tongue with papules, and laboratory studies indicated a direct hyperbilirubinemia. Admitted for evaluation, he developed continuous fever, increasing maculopapular rash, and subsequent desquamation of hands and feet. He ultimately met criteria for incomplete KD, was treated with intravenous immunoglobulin, and avoided cardiac complications. This presentation of incomplete KD with hyperbilirubinemia is rare because the patient was afebrile at ED presentation.


2014 ◽  
Vol 30 (7) ◽  
pp. 491-492 ◽  
Author(s):  
Brit L. Anderson ◽  
Amy B. Guiot ◽  
Nathan L. Timm

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