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Oral Rhabdomyomatous Hamartoma in a Paediatric Patient: Case Report a Rare Lesion
Érika Machado do Carmo Albuquerque1, Letícia Albuquerque Rodrigues1, Gislayne Nunes de Siqueira2
1Postgraduate Program in Health Sciences, Federal University of Ceará - Sobral Campus, Sobral, Brazil.
Background:
Rhabdomyomatous hamartoma is a rare congenital lesion, usually described on the face and neck and infrequently found in the oral cavity. Because its clinical presentation is non-specific, histopathological examination plays a fundamental role in establishing the final diagnosis and determining appropriate therapeutic management.
Case Report:
An 8-year-old male patient presented with a submucosal nodule on the left lateral border of the tongue. The initial diagnostic hypothesis was dermoid cyst; however, histopathological examination revealed thick, interlacing bundles of skeletal striated muscle, compatible with rhabdomyomatous hamartoma.
Conclusion:
Although rare, rhabdomyomatous hamartoma should be considered in the differential diagnosis of oral nodules in children. Histopathological confirmation is essential for accurate diagnosis and as a guide to treatment, helping to avoid unnecessary interventions and ensuring proper management of the lesion.