Neurofibroma is an uncommon benign
tumor arising from nerve sheath fibroblasts. The diagnosis of solitary lesions becomes difficult in patients who do not have any family history of
neurofibroma. An intra-oral solitary
neurofibroma comprises 6.5% of reported cases of
neurofibroma. Few cases of intraosseous solitary
neurofibroma have been published as per literature. Treatment-surgical resection of
tumor has an excellent prognosis with extreme rare malignant transformation which is more commonly seen in
neurofibromatosis. A periodic follow-up is necessary in solitary
tumors to rule out syndromic cases.
Leiomyoma is a benign
tumor of smooth muscle origin, which is usually diagnosed in the gastrointestinal tract, uterus, and skin. The most effective treatment for solid, vascular, and epithelioid
angioleiomyomas is surgical resection along with
tumor capsule. Here we report an uncommon occurrence of multiple benign
tumors in a pediatric patient.