adenoid ameloblastoma with dentinoid is a rare odontogenic tumor. granular cell ameloblastoma also is a less common histological subtype of ameloblastoma. in this report, the patient was a 31‑year‑old male. the lesion was located in the right mandible and was unicystic with well‑defined borders. the tumor tissue was showing a combination of follicular, plexiform, and desmoplastic patterns of am...

Congenital gingival granular cell tumors (CGGCT) are rare lesions which have occasionally been reported in India. It is an uncommon benign soft tissue lesion that usually arises from alveolar mucosa of neonates and causes respiratory and feeding problems. Due to its clinical features and treatment approaches these cases have aroused interest of different disciplines. We reported a case of a 4 d...

Ameloblastoma is a slow-growing and locally invasive epithelial odontogenic tumor of the jaw that runs benign course in most cases. Granular cell ameloblastoma rare subtype ameloblastoma, showing granular transformation its cytoplasm. It considered as an aggressive variant ameloblastoma. Herein, we report case 34-year-old male patient who presented with swelling left cheek for 1-year duration r...

Congenital epulis (CE) or "Granular cell epulis" also previously termed as "Neumann's tumor" is a benign growth arising from the mucosa of the gingiva, typically seen as a mass protruding from the infant's mouth, often interfering with respiration and feeding. These tumors generally present as a single mass arising from the upper alveolus. We report a rare case of two congenital epulides arisin...

Congenital epulis of the newborn is a rare gingival tumor that occurs along the alveolar ridge. We report the prenatal sonographic and postnatal MR imaging findings in an infant with maxillary and mandibular congenital epulides.

Congenital granular cell epulis (CGCE) is a very rare benign soft tissue lesion of the neonate, it most frequently located on the anterior maxillary alveolar ridge. It has a female predilection. It is a tumor with no tendency to recur after excision. The exact histogenesis of this tumor remains unresolved and it may be hamartomata.