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Osteopetrosis complicated by osteomyelitis of the maxilla: A rare case report and review of the literature
(Wroclaw Medical University, 2020)
Osteopetrosis is a rare hereditary bone disorder that results in an increase in bone density due to gene
mutations and osteoclastic dysfunction. This may lead to cranial nerve compression, bone fractures and
osteomyelitis. ...
Mucoepidermoid carcinoma ex pleomorphic adenoma: A rare diagnostically challenging entity
(Elsevier, 2022)
Mucoepidermoid carcinoma (MEC) arising in pleomorphic adenoma (PA) is an extremely rare entity. Involvement of minor salivary glands by this entity has only being described twice previously. We report on a diagnostically ...