A girl with extremely refractory Kawasaki disease: an instructive case with unusual course and outcome

2011 ◽  
Vol 22 (4) ◽  
pp. 461-465 ◽  
Author(s):  
Kossiva Lydia ◽  
Karanassios Evangelos ◽  
Papadopoulos George ◽  
Karavanaki Kyriaki

AbstractKawasaki disease constitutes an acute febrile vasculitis of unknown aetiology. It is considered the most common cause of acquired cardiac failure in children. Although standard treatment comprises intravenous immunoglobulin and aspirin, some children exhibit refractory disease, necessitating the use of alternative therapies such as corticosteroids and anti-tumour necrosis factor-alpha. For these cases, few controlled data are available. This report focuses on an extremely refractory classical Kawasaki disease with coronary artery aneurysms and ongoing inflammation. We discuss the therapeutic approaches and the potential pitfalls undertaken, which led to an unfavourable clinical outcome.

2021 ◽  
Vol 97 (5) ◽  
pp. 259-264
Author(s):  
Ágnes Kinyó ◽  
◽  
Norbert Wikonkál

Complex multifactorial pathogenesis of hidradenitis suppurativa eventually results in chronic inflammation of the apocrine gland-bearing areas of the skin. However, the pathogenesis is not fully understood, there are many immune cells and inflammatory pathways of which role is clearly defined in the last years in HS, such as interleukin 1β (IL-1β), tumour necrosis factor alpha (TNFα), IL-17, IL-12 and IL-23. These pathways provide multiple targets for medical treatment. Currently, only adalimumab is licenced in HS, but the numerous ongoing clinical trials promise huge potential therapeutic options in this debilitating disease.


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