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    A case report: Ludwig's angina in a patient with systemic lupus erythematosus (SLE) and familial mediterranean fever (FMF)
    (University of Dicle, 2014) Yalcin M.; Atilgan S.S.; Yaman F.; Lacin N.; Aslan N.; Günes N.; Unsal H.Y.
    Ludwig's angina is potentially life-threating, rapidly spreading involving bilaterally submandibular, sublingual and sub mental spaces. It is characterized by induration of mouth, swelling, elevation of tongue and airway obstruction. There is three main points with early diagnosis which are airway management, intravenous antibiotic therapy and surgical intervention. We present a case of Ludwig's angina in a 14-year-old boy. The etiology, management and potential complications of Ludwig's angina are discussed.
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    Maxillary unicystic ameloblastoma: A rare case report
    (University of Dicle, 2018) Lacin N.; Yalcin M.; Efeoglu B.F.; Tumen E.C.
    Ameloblastoma is an aggressive neoplasm of benign odontogenic origin. It is the second common odontogenic neoplasm. Based on clinical, radiographic, histopathology, behavioral and prognostic features, they are classified as four types which are unicystic ameloblastoma (UA), peripheral ameloblastoma, desmoplastic ameoblastoma and solid/multicystic ameloblastoma. UA is a rare odontogenic tumor with clinical and radiographic. It is generally occurs in posterior mandibular ramus. In our case, we present a rare case of maxillary unicystic ameloblastoma in a 16 year-old male patient has been treated by surgical enucleation. © 2018 University of Dicle.
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    The typical appearance and CBCT images of the patient with Papillon-Lefevre syndrome: A case report
    (University of Dicle, 2015) Tumen D.S.; Tumen E.C.; Gunay A.; Lacin N.; Cetin S.G.
    Papillon-Lefevre syndrome is a rare autosomal recessive genetic disorder, which is transmitted with an estimated frequency of one to four per million individuals. It is characterized by palmar-plantar hyperkeratosis, and rapid destruction of the alveolar bone and periodontium of both the primary and permanent dentitions, commencing at the time of tooth eruption. Early diagnosed and rehabilitation of children with Papillon-Lefevre syndrome will go a long way in helping them interact normally and integrate with their peers. However, the rarity with which this entity appears, along with its complex characteristics, often make it difficult to treat. The aim of this case report is to present the early diagnosed of a 5-year-old boy with Papillon-Lefevre syndrome associated with severe periodontitis in which the premature exfoliation of primary maxillary and mandibular incisor teeth and maxillary primary first molars are observed, and with hyperkeratosis of the palms, knees and soles.