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Öğe A different harlequin color change case(OrtadogŸu Reklam Tanitim Yayincilik Turizm Egitim Insaat Sanayi ve Ticaret A.S., 2017) Demirkan S.; Gündüz Ö.Harlequin colour change is a transient condition that alarms parents usually. The skin area that infant lay on is erythematous, other part is pale and there is a sharp boundary in the middle of the body. Sometimes it does not occur on face and genital area, mucous membranes. Erythema and pallor replace by changing position. It is thought that the cause of it is vasodilatation due to lack of vascular tone depending on immature hypothalamic or sympathetic system. It is also reported that this condition may develop depending on traumas preponderant to sympathetic chain, tumours and vascular pathologies. We have reported a case due to it has differences about clinical presentation between other reported cases. Copyright © 2017 by Türkiye Klinikleri.Öğe Hughes-Stovin syndrome as an outcome of Behçet disease or as a different entity(Korean Society for Thoracic and Cardiovascular Surgery, 2018) Demirkan S.; Gültekin Y.Hughes-Stovin syndrome is a rare disorder of unknown etiology. Although the association between multiple pulmonary artery aneurysms and venous thrombosis of the lower limbs was reported by Beattie and Hall in 1911, it was not until 1962 that the eponym "Hughes-Stovin syndrome" was formally introduced in the medical literature. We describe 2 patients with Hughes-Stovin syndrome who presented with pulmonary artery aneurysm, thrombophlebitis, hemoptysis, and oral ulcers, review the manifestations of the disease, and compare its similarities with and differences from Behçet disease. © The Korean Society for Thoracic and Cardiovascular Surgery. 2018.Öğe Management of a Recurrent Pyogenic Granuloma of the Inferior Lip with Pulsed Dye Laser: A Case Report(Elsevier Inc., 2016) Demirkan S.Pyogenic granuloma (PG) is a common, acquired, benign vascular reactive proliferation. This article presents the unique and successful pulsed dye laser treatment of a labial PG on a 60-year-old patient. © 2017 Elsevier Inc.Öğe Relapsing polychondritis misdiagnosed and treated as a “soft tissue infection” and a brief review of diagnostic clinical clues(OrtadogŸu Reklam Tanitim Yayincilik Turizm Egitim Insaat Sanayi ve Ticaret A.S., 2017) Gündüz Ö.; Demirkan S.; Samav G.; Arslan H.; Çakartaş R.Relapsing polychondritis (RPC) is a rare immune-mediated disease, which targets particularly the cartilaginous tissue. At the initial stages of RPC, recurring mild-inflammatory attacks targeting the ears, nose, eyes, joints and respiratory tract can be observed but as the disease progresses, aortic and/or mitral valvular regurgitation (AR/MR) or life-threatening tracheobronchomalacia (due to involvement of aortic, mitral valves and/or trachea) may occur, as well as severe destruction of the ear, nose, etc. RPC may coexist with other diseases, such as systemic vasculitides, Graves disease or myelodysplastic syndrome. Establishing an early diagnosis is of utmost importance to prevent the development of AR/MR, or tracheobronchomalacia by preserving the cartilage tissue and also to diagnose a possible coexisting disease. Patients, particularly at the initial stages of the disease may object to a skin biopsy due to concerns for visible scars. Therefore, a good grasp of RPC's clinical symptoms may facilitate to establish an early diagnosis. Copyright © 2017 by Türkiye Klinikleri.Öğe Sorafenib-asssociated hand-foot syndrome treated with topical calcipotriol(Elsevier Inc, 2017) Demirkan S.; Gündüz Ö.; Devrim T.[No abstract available]
