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Published on: April 15, 2021
Coronary aneurysms in a child: an unusual presentation of pseudovasculitis
Luciana P C Seguro1, Jozelio Freire de Carvalho, Alessandro C Lianza
1Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil. lucianapc@gmail.com
Insights
Kawasaki disease can cause coronary artery aneurysms in children. A rare case highlights pheochromocytoma as a cause of these aneurysms, mimicking vasculitis and resolving after tumor removal.
Area of Science:
- Pediatric Cardiology
- Pediatric Endocrinology
- Pediatric Oncology
Background:
- Kawasaki disease is the leading cause of acquired pediatric coronary artery disease.
- Coronary artery abnormalities are uncommon in children.
- Pheochromocytoma is a rare tumor causing hypertension.
Observation:
- A female child presented with coronary artery aneurysms and convulsions, initially diagnosed with Kawasaki disease.
- Despite treatment for Kawasaki disease, hypertension and inflammation persisted.
- Further investigation revealed a pheochromocytoma.
Findings:
- Surgical removal of the pheochromocytoma normalized blood pressure and inflammatory markers.
- Coronary aneurysms progressively reduced, normalizing within 8 months.
- This case represents the first description of pheochromocytoma-associated coronary aneurysms presenting as pseudovasculitis.
Implications:
- Pheochromocytoma should be considered in pediatric cases of coronary aneurysms with persistent hypertension and inflammation.
- Early diagnosis and surgical management of pheochromocytoma can lead to resolution of coronary aneurysms.
- This finding expands the differential diagnosis for pediatric vasculitis syndromes.
Abstract:
Abnormalities of the coronary arteries in children are rare and Kawasaki disease is the most common cause of acquired coronary disease in a paediatric population. We report a case of a female child with coronary artery aneurysms and convulsions, who was diagnosed with Kawasaki disease. Due to systemic arterial hypertension and persistence of high inflammatory markers after treatment with high dose glucocorticoid and intravenous immunoglobulin, further investigation was performed and revealed a pheochromocytoma. Surgical removal led to normalization of blood pressure and laboratory parameters. Periodic echocardiography studies revealed progressive reduction of coronary aneurysms, with complete normalisation after 8 months. This is the first case described of coronary aneurysms presenting as a pseudovasculitis syndrome associated with pheochromocytoma.
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