History and exam

Key diagnostic factors

common

presence of risk factors

Key risk factors include Asian ancestry, age 3 months to 4 years, and male sex.

polymorphous rash

Non-specific polymorphic rash. This is usually a diffuse, maculopapular erythematous rash. Occasionally scarlatiniform- or erythema multiforme-type rash with target lesions on the arm and trunk.

Groin erythema or desquamation and fine pustules over extensor surfaces of extremities can occur.

conjunctival injection

The patient has a history or presents with non-purulent non-exudative bilateral conjunctival injection (in 90% of cases).

Less common are episcleritis or uveitis (anterior and/or posterior).

mucositis

History or physical findings of dry, erythematous, fissured lips that bleed easily, erythema of the oral and pharyngeal mucosa, and strawberry tongue with prominent papillae and erythema (alone or in combination in 90% of cases). Oral exudation or Koplik spots are not present and oral ulceration would be atypical. Strawberry tongue may be present, but oropharyngeal/mucosal changes may be variable.

skin changes in the peripheral extremities

Initial erythema and oedema may be present, usually of palms and soles. Typically the skin on wrists and ankles would not be involved. Peripheral changes may be acute (swelling and erythema) as well as subacute (desquamation).

Periungual desquamation of fingers and toes about 2 weeks after onset may be seen, as may transverse grooves across the nails (Beau lines) 1 to 2 months after onset.

enlarged cervical lymph nodes

Unilateral lymphadenopathy is observed in approximately 40% of patients, with node diameter above 1.5 cm.

The overlying skin may be erythematous. The node is not fluctuant or purulent and is unresponsive to antibiotics.

coronary artery aneurysms

Coronary artery abnormalities (mainly aneurysms) develop in approximately 20% to 25% of untreated patients.

fever and extreme irritability

Fever usually over 39°C (102°F). Most patients present because of prolonged fever of at least 5 days in duration with often abrupt onset. Fever is unresponsive to antibiotics, if given. Patients are often irritable beyond that expected for the extent of fever.

There is an associated significant irritability. During this acute phase, many patients will develop poor intake, abdominal pain, nausea, and diarrhoea.

Other diagnostic factors

uncommon

pericarditis with effusion

Not part of the diagnostic criteria.

congestive heart failure

Not part of the diagnostic criteria.

joint pain or oedema

Arthralgia and arthritis involving multiple joints (e.g., including hands, knees, ankles, and hips) are more common if intravenous immunoglobulin treatment is delayed.

neurological manifestations

Headaches and stiff neck (secondary to aseptic meningitis), facial palsy, and cerebral infarction are rare, but can occur.

gastrointestinal manifestations

Abdominal pain, vomiting, pseudo-obstruction, diarrhoea, hepatitis, obstructive jaundice, gallbladder distension or hydrops of the gallbladder, and pancreatitis are rare clinical findings. Gastrointestinal symptoms may precede typical Kawasaki disease symptoms.[35]

urological manifestations

Sterile pyuria is the most common, but meatitis, urethritis and vulvitis (in females), proteinuria, nephritis, and acute renal failure can occur.

other dermatological manifestations

Peripheral extremity gangrene, pustules, erythema multiforme-like lesions, perianal desquamation, macules, papules, measles-like rash, and scarlet fever-like erythema are rare clinical findings.

Risk factors

strong

Asian ancestry

KD is most common in Asian children, especially those of Japanese descent.

Some cases of KD show familial susceptibility. Children in Japan who have parents with KD seem to have a more severe form of this disease and are more susceptible to recurrence.

KD likely has a genetic susceptibility. Genome-wide multipoint linkage analysis of affected sibling pairs in Japan identified evidence of linkage at chromosome 12q24.[27]

age 3 months to 4 years

Most patients (80%) with KD are aged <5 years.[1][3] It is rare in infants aged <3 months, and has been rarely described in adolescents and adults.

In the US the peak age of onset is 13-24 months. In Japan, the peak age of onset is 6-11 months.[13]

weak

male sex

Disease occurs more often in males than in females (1.5:1).[3][28]

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