Haemophiliac Pseudotumour of Oral Cavity: Case Report with Review of Literature

Haemophilic pseudotumour is a rare entity among neoplasms in the oral cavity. It is a diagnostic and treatment challenge for the surgeons. Clinically, the tumour mimics innocuous soft tissue lesions like fibroma, lipoma or pyogenic granuloma with intermittent bleeding which can be misleading.

Haemophiliac 30-year-old male patient complained of slow-growing sessile and pedunculated growth on left molar region of gingiva buccally and lingually, which bleeds intermittently in the last 4 months.

Clinically and histopathologically diagnosed as pseudotumour of haemophilia treated with surgical excision and haematological intervention and concurrent treatment challenges with successful surgical outcome.

Management is crucial as surgical curettage should be done in consensus with haematological correction and supportive care. Post-operative period should be alarmed for haemorrhage as it can hinder healing and cause recurrence.