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Kawasaki disease

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Kawasaki disease (KD) was first reported in 1967 by T. Kawasaki , a Japanese pediatrician.1 The first Korean KD patient was reported in february 1973. Since then, the incidence of this disease has increased continuously. KD is characterized with acute systemic vasculitis that occurs predominantly in children between 6 months to 5 years of age. Although the clinical symptoms of KD are well characterized, the causes of this disease are not yet known. For this reason, KD is usually diagnosed by clinical symptoms, such as a fever for 5 days or more, bilateral nonpurulent conjunctival congestion, changes of the lips and oral mucosa, polymorphous exanthema along the trunk, changes of the peripheral extremities and subsequent desquamation of finger tips, and nonpurulent cervical lymphadenopathy over 1.5 cm in size [1]

High-dose of aspirin can agravate further including sensorineural hearing loss. Various authors suggested that the ototoxicity of the high-dose aspirin that was used for the treatment of the acute phase might cause sensorineural hearing loss.[2]

Links

Park et al.Sensorineural hearing loss in patients with Kawasaki disease Korean J Pediatr. 2015 Nov; 58(11): 434

Chest pain

Aneurisma

Ghareep et al. 2015 Kawasaki Disease: Diagnosis and Follow-Up by CT Coronary Angiography with the Use of 128-Slice Dual Source Dual Energy Scanner. A Case Report Pol J radiol. 80:526-528

Disease classification WHO
M30.3 Kawasaki´s syndrome
ICD 10 classification'

Q265936 op Wikidata  Interwiki via Wikidata


References

References: