Kawasaki disease with peritonsillar abscess as the first symptom: A case report

Li-Man Huo1, Li-Min Li2, Hao-Yang Peng3

  • 1Department of Pharmacy, The Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, Hebei Province, China.

PubMed

Insights

Kawasaki disease (KD) can present with rare symptoms like abscesses, mimicking infections. Early KD diagnosis and treatment with immunoglobulin and aspirin are crucial for preventing severe cardiovascular complications.

Area of Science:

  • Pediatric Vasculitis
  • Infectious Disease Mimicry

Background:

  • Kawasaki disease (KD), or mucocutaneous lymph node syndrome, is an acute vasculitis affecting medium and small arteries.
  • KD can lead to severe cardiovascular complications, including coronary artery aneurysms in 25% of cases.
  • Peritonsillar abscesses are a rare but significant symptom of KD, often leading to misdiagnosis.

Observation:

  • A 5-year-old boy presented with fever, neck pain, and difficulty opening his mouth, initially treated as a throat infection.
  • Despite antibiotic therapy for suspected periamygdala abscess and sepsis, the patient's condition did not improve.
  • The patient later developed classic KD symptoms: conjunctival congestion, prune tongue, perianal congestion, desquamation, and swollen bunions.

Findings:

  • The initial presentation and treatment failure for presumed deep neck infection prompted further investigation.
  • A definitive diagnosis of Kawasaki disease was established based on the evolving clinical presentation.
  • Complete remission was achieved following treatment with intravenous immunoglobulin.

Implications:

  • Neck pain and lymphadenopathy in children may be misdiagnosed as deep neck infections, delaying appropriate KD treatment.
  • Clinicians should consider KD in unexplained neck infections, avoiding premature invasive procedures.
  • Prompt diagnosis and treatment of KD with aspirin and immunoglobulin are vital to prevent coronary artery abnormalities.
Abstract

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