http://hdl.handle.net/11513/94 Dahili Tıp Bilimleri Bölümü'ne ait koleksiyonları içerir. 2026-04-12T02:19:50Z http://hdl.handle.net/11513/337 Lack of effectiveness of keratin dressings in epidermolysis bullosa Sürücü, Hacer Altun; Yeşilova, Yavuz; Turan, Enver; Aksoy, Mustafa; Tanrıkulu, Osman; Eroğlu, Naime 2015-01-01T00:00:00Z http://hdl.handle.net/11513/258 The Sociodemographic, Living and Environmental Characteristics of Patients with Cutaneous Leishmaniasis Aksoy, Mustafa; Yeşilova, Yavuz; Sürücü, Hacer Altun; Ardıç, Nurettin; Yeşilova, Abdullah Background: Cutaneous leishmaniasis is a parasitic skin disease caused by various leishmaniasis species. Material and Methods: In this study, the clinical, sociodemographic, living and environmental characteristics of 4048 cutaneous leshmaniasis patients are presented. A retrospective evaluation was made of 4048 cutaneous leishmaniasis patients in terms of gender, lesion diameter (mm), number of lesions, duration of lesions (weeks) and living conditions, then statistical analysis was applied. Results: The cutaneous leismaniasis patients comprised 52.47% female and 47.53% males with a mean age of 16.48±0.23 years. The mean duration of the disease was 9.62±0.33 weeks, lesion diameter was 12.197±0.10 mm and mean number of lesions was 1.75±0.02. The number of people in the patient’s family was generally 5-10 and the number of rooms in the house was 2-3 for 70.63% of patients. The vast majority of the cutaneous leishmaniasis patients, 96.96%, lived in a lowland plains area and no patient lived in wetlands. The types of houses were of concrete construction in 94.94% and stone in 1.61% and 1.41% lived in an apartment block. Animals were reported to be kept in the living area of 17.02% of patients and of those, 2.30% had a WC. Conclusion: The determination of an excessive number of Phlebotomus in areas of low socio-economic living conditions and the high incidence of cases in these areas has revealed a direct, positive relationship between cutaneous leishmaniasis disease and the socio-economic conditions of the patients. 2017-01-01T00:00:00Z http://hdl.handle.net/11513/257 The frequency of laryngeal involvement in lipoid proteinosis patients Yükkaldıran, Ahmet; Aksoy, Mustafa; Yeşilova, Yavuz; Demir, Mahmut; İynen, İsmail; An, İsmail; Tanrıkulu, Osman Aim: Lipoid proteinosis (LP) is a rare autosomal recessive disorder that occurs with the accumulation of hyaline substance in oral cavity, laryngeal mucosa and skin. The aim of this study was to investigate the incidence of laryngeal involvement in patients with LP which have hoarseness and skin lesions, and the areas of hyaline substance accumulation in the larynx. Material and Methods: In this study, 21 patients who were admitted to our Dermatology outpatient clinic between January 2013 and December 2017 and diagnosed as LP with punch biopsy were evaluated. Laryngeal imaging was performed in otorhinolaryngology clinic, and the frequency of larynx involvement and the areas of hyaline accumulation in the larynx were evaluated. Results: Twenty-one patients with hoarseness and diagnosed by skin biopsy as LP were included in the study. Thickening of the vocal cords in 21 patients (100%); thickening and hypertrophic changes of arytenoids in 13 patients (61.9%); thickening and hypertrophic changes of the interarytenoid area in 10 patients (47.6%); thickeningand hypertrophic changes of epiglottis in 3 (14.3%) patients; hypertrophic changes and thickening of the aryepiglottic fold in 3 patients (14.3%); thickening and hypertrophic changes of ventricular folds in 2 patients (9.5%) were observed. Conclusion: In our study, similar to the data in the literature, the pathological changes were most frequently seen in the vocal cords and the least in the ventricle band, aryepiglottic fold and epiglottis. In order to better understand the laryngeal involvement and the areas of involvement in LP patients, studies with more patients are needed. 2019-01-01T00:00:00Z http://hdl.handle.net/11513/256 Skrotal Dil, Periferik Fasyal Paralizi ve Orofasiyal Ödem Triadı: Melkersson – Rosenthal Sendrom Aksoy, Mustafa; Yeşilova, Yavuz; Tanrıkulu, Osman; Coşkur, Naime; Doğan, Sibel Melkersson Rosenthal sendromu tekrarlayan periferik fasiyal paralizi, orofasiyal ödem ve fissürlü dil triadı ile karakterize granülomatöz bir hastalıktır. Etiyolojisi tam olarak bilinmemektedir. Tedavide topikal ve sistemik medikal tedavilerin yanında cerrahi müdahaleler de gerekebilmektedir. Klasik triadın aynı anda görülmesi nadirdir. Bu olguda kalsik triada ait 3 bulgunun da aynı andan görüldüğü 19 yaşında bayan hasta sunulmaktadır. 2016-01-01T00:00:00Z