Osteoblastoma of Mandible:A Rare Clinical Presentation

osteoblastoma of mandible:a rare clinical presentation

Neurofibroma: Report of a rare clinical presentation

Neurofibroma is a tumor composed of a complex proliferation of neuromesenchymal tissue (Schwann cells, perineural cells, fibroblast, and mast cells). We report a 45-year-old female who had a slow growing, large, soft, pedunculated mass on her left lateral neck. A skin biopsy confirmed the diagnosis of neurofibroma.

Asymptomatic Osteoblastoma of the Mandible: A Rare Case Report

Osteoblastoma is a rare solitary osteoblastic bone neoplasm. It is characterized by proliferation of osteoblasts forming trabeculae within a vascular fibrous stroma. There is a variety of jaw bone lesions with very close clinical, radiological and microscopic interrelations, which make diagnosis more challenging. Familiarity with these rare bony lesions is vital for oral pathologists. This repo...

Sheehan’s syndrome presenting as psychosis: a rare clinical presentation

 Sheehan’s syndrome (SS) refers to the occurrence of varying degree of hypopituitarism after parturition (1). It is a rare cause of hypopituitarism in developed countries owing to advances in obstetric care and its frequency is decreasing worldwide. However, it is still frequent in underdeveloped and developing countries. Sheehan’s syndrome is often diagnosed late as it evolves slowly (2,3). Re...

Periosteal Osteoblastoma of the Pelvis: A Rare Case

Among the rare bone tumors, the osteoblastoma is a fascinating tumor. The rarity, the predisposition to occur in any bone and the diagnostic dilemma makes this infrequent tumor interesting. It is sporadically reported in the literature and what is rarer is its occurrence in the pelvis. The unusual location and inconclusive radiographic findings with diffused diagnostic evidences delays the mana...

Epithelioid osteoblastoma or aggressive osteoblastoma of the astragalus. Presentation of a case and revision of clinical and pathological symptoms