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    Congenital Insensitivity to Pain with Anhidrosis Syndrome: A Case Report
    (Galenos Yayincilik, 2014) Turan, Hakan; Besir, Fahri Halit; Uslu, Esma; Basar, Feyza; Gun, Emrah; Gecer, Yavuz
    Congenital Insensitivity to Pain with Anhidrosis syndrome is a rare, autosomal recessively inherited syndrome caused by neurotrophic tyrosine receptor kinase 1 gene mutation. The basic findings of the syndrome are absence of pain sense, anhidrosis, and self-destructive behaviors. Herein, we describe a 4-year-old boy presented with xerosis, anhidrosis, and traumatic lesions on the hands and diagnosed as Congenital Insensitivity to Pain with Anhidrosis syndrome. On the occasion of this case, we aimed to review general and dermatological characteristics of this rare syndrome.
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    LIFE-THREATENING ANGIOMYXOMA OF THE LARYNX
    (Jimma Univ, Ethiopia, 2015) Yaman, Huseyin; Erdem, Havva; Belada, Abdullah; Besir, Fahri Halit; Oktay, Murat; Uzunlar, Ali Kemal
    BACKGROUND: Angiomyxoma is a benign proliferative mesenchymal tumor and a very rare mass in the larynx. There is not enough information about the etiology, clinical finding, treatment and prognosis of laryngeal angiomyxoma. CASE DETAILS: A 52 years old man presented with respiratory distress. Also, he had suffered from dysphagia, dysphonia, cough, and obstructive sleep apnea in the supine position for 6 months. He was operated on via transoral approach under general anesthesia with orotracheal intubation. The mass was encapsulated and completely removed. The histopathologic diagnosis was reported as angiomyxoma. CONCLUSION: Angiomyxoma should be considered in the differential diagnosis of the larynx masses. The treatment of angiomyxomas of the larynx is surgical. The mass can be usually excised intraorally or endoscopically.