Wos İndeksli Açık & Kapalı Erişimli Yayınlar
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Item Sliding hiatal hernia mimicking a left atrial mass(2019) Kocabas, Umut; Ozkalayci, Flora; Altun, Armagan; 0000-0002-3233-8263; 0000-0001-6424-9399; 32082840; ABB-5844-2020; AAG-5856-2020Item Ga-68-DOTA-TATE in Neuroblastoma With Marrow Involvement(2019) Torun, Nese; 30889003A 22-month-old boy diagnosed with neuroblastoma was evaluated by bone scintigraphy and I-123-metaiodobenzylguanidine scintigraphy, and no metastases to skeletal system was detected. However, plain radiograph and MRI revealed suspected metastatic lesions. The patient was therefore evaluated by Ga-68-DOTA-TATE PET/CT, and Ga-68-DOTA-TATE uptake was observed in multiple bone and bone marrow areas, which were consistent with metastases. Biopsy was taken from the right iliac bone, and the pathological examination of the biopsy specimen was coherent with neuroblastoma invasion.Item Antibiotic overconsumption and resistance in Turkey(2019) Isler, B.; Keske, S.; aksoy, M.; Azap, O. K.; Yilmaz, M.; Yavuz, S.S.; Aygun, G.; Tigen, E.; Akalin, H.; Azap, A.; Ergonul, O.; 30844434organizational unit.listelement.badge Cardiac biomarkers in coronary slow flow: Endocan and omentin-1(2019) Okyay, Kaan; 31219435; AAK-7355-2020Item Aggressive metastatic malignant pilomatrixoma followed by F-18-FDG PET/CT(2019) Torun, Nese; Canbolat, Emine Tuba; 30424974Item Celebrating the 25th anniversary of the International Conference on Population and Development: A perspective from Turkey(2019) Akin, Ayse; Ali, Moazzam; 31709532Item 35-year Onset of a Squamous Cell Carcinoma Originating from Sacral Pilonidal Sinus(2019) Ozkan, Burak; Cologlu, Harun; Uysal, Cagrı A.; Ertas, Nilgun M.; 32537300Item Amyloid Goiter Due to Familial Mediterranean Fever in a Patient with Byler Syndrome: A Case Report(2014) Cigerli, Ozlem; Unal, Asli Dogruk; Parildar, Hulya; Demiralay, Ebru; Tarcin, Ozlem; 25337425Background: Familial Mediterranean Fever (FMF), also inherited with autosomal recessive trait, is characterized by recurrent episodes of fever, arthritis, and serositis. Congenital Byler Syndrome (Progressive Familial Intrahepatic Cholestasis) inherited with autosomal recessive trait and characterized by defective secretion of bile acids. FMF associated Amyloid A deposition occurs in many tissues and organs, but amyloid goiter is a rare entity that leads to enlargement and dysfunction of the thyroid. Case Report: We present a rare case of 24 year old male patient who had liver and kidney transplantation due to Byler Syndrome and secondary amyloidosis related to FMF, diagnosed as rapidly growing large amyloid goiter. Deposits of extracellular amyloid and dense adipose metaplasia diagnostic for amyloid goiter are determined upon histopathological examination of thyroidectomy material. Conclusion: When goiter was detected in cases with history of systemic amyloidosis and rapidly growing goitre, amyloid goiter should be remembered at first. This case is unique since two autosomal genetic disorders are together in the same patient and important as it emphasizes the consequences of consanguineous marriage, early diagnosis and treatment compliance of FMF and the awareness of amyloid goiter in patients followed by primary care physicians and healthcare professionals.Item Intrathecal Methotrexate-Induced Posterior Reversible Encephalopathy Syndrome (PRES)(2014) Guler, Tulay; Cakmak, Ozden Yener; Toprak, Selami Kocak; Kibaroglu, Seda; Can, Ufuk; 24764745