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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.
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.
Background:
Kawasaki disease (KD), also known as mucocutaneous lymph node syndrome, is an acute, self-limiting vasculitis of unknown aetiology that mainly involves the medium and small arteries and can lead to serious cardiovascular complications, with a 25% incidence of coronary artery aneurysms. Periton-Sillar abscesses are a rare symptom of KD and is easily misdiagnosed at its early stages.
Case Summary:
A 5-year-old boy who presented to a community hospital with a 3-d fever, difficulty in opening his mouth, and neck pain and was originally treated for throat infection without improvement. On the basis of laboratory tests, ultrasound of submandibular and superficial lymph nodes and computed tomography of the neck, the clinician diagnosed the periamygdala abscess and sepsis that did not resolve after antibiotic therapy. On the fifth day of admission, the child developed conjunctival congestion, prune tongue, perianal congestion and desquamation, and slightly stiff and swollen bunions on both feet. A diagnosis of KD was reached with complete remission after intravenous immunoglobulin treatment.
Conclusion:
Children with neck pain, lymph node enlargement, or airway obstruction as the main manifestations are poorly treated with intravenous broad-spectrum antibiotics. Clinicians should not rush invasive operations such as neck puncture, incision, and drainage and should be alert for KD when it cannot be explained by deep neck space infection and early treatment with aspirin combined with gammaglobulin.
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