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Öğe Ankylosing spondylitis with mycetoma case treated with oral itraconazole (Rheumatology International DOI: 10.1007/s00296-009-1088-z)(2010) Bekci T.; Kesli R.; Maden E.; Ozbek O.[Abstract not Available]Öğe Anomalous right coronary artery originating from the left sinus of Valsalva: Rare but outstanding cause of syncope [Sol sinüs Valsalvadan köken alan sa? koroner arter anomalisi: Nadir ama senkobun göze çarpan nedeni](2013) Sonmez O.; Karaarslan S.; Elvin Gul E.; Ozbek O.; Ozdemir K.Coronary anomalies are relatively common but rarely associated with syncope, myocardial ischemia, and sudden cardiac death. An anomalous right coronery artery from the left sinus of valsalva is now recognized as an important causative factor in sudden death and myocardial infarction and syncope.This case report presents an anomalous right coronary artery (RCA) originating from the left sinus of Valsalva with syncope and will be focused on the diagnostic variation and management.Öğe Giant hepatic angiomyolipoma mimicking hepatocellular carcinoma [Hepatoselüler kanseri taklit eden dev hepatik anjiyomiyolipom](TIP ARASTIRMALARI DERNEGI, 2014) Gungor G.; Kayacetin E.; Biyik M.; Ozbek O.; Ucar R.; Baba F.; Demir A.Angiomyolipomas (AMLs) are a benign mesenchymal tumor that typically occurs in the kidney and very rare in the liver. Even though these tumors can be diagnosed with imaging tecniques, diagnosis mainly relies on pathological findings. Because AMLs can mimic other hepatic tumors such as hepatocellular carcinoma (HCC) on radiologic images due to some of the features. We presented a giant hepatic AML case which mimicing hepatocellular carcinoma in imaging techniques. We suspected from hepatocellular carcinoma according to radiologic images, but biopsy result was hepatic angiomyolipoma. There are potential risks such as spontaneous rupture and malignant transformation of these tumors. The effective therapy of hepatic AML is surgical resection.Öğe Spontaneous retroperitoneal hemorrhage presenting as hemoperitoneum secondary to renal cyst rupture in a peritoneal dialysis patient with acquired cystic kidney disease(Medknow Publications, 2015) Biyik Z.; Solak Y.; Gaipov A.; Ozbek O.; Esen H.; Turk S.Spontaneous retroperitoneal hemorrhage (SRH) is a rare and potentially fatal condition. Acquired cystic kidney disease (ACKD) may cause SRH in hemodialysis patients. However, presentation of retroperitoneal hematoma as hemoperitoneum in peritoneal dialysis (PD) patients is exceedingly rare. We report a 44-year-old male PD patient who presented with hemoperitoneum secondary to retroperitoneal hematoma. The reason of SRH was rupture of the cysts of ACKD. The patient underwent unilateral nephrectomy with subsequent disappearance of hemoperitoneum. The importance of this case lies in the fact that the patients who have been receiving dialysis for a long time should be under surveillance in terms of ACKD development and potential associated complications such as cyst hemorrhage and malignancy.
