Serkan Gokcay

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INTRODUCTION Familial Mediterranean fever is an autosomal recessive disease that predominantly affects people of the Mediterranean coast. One of the most frequent complications of the disease is amyloidosis. This clinical entity is known as secondary (also called AA) amyloidosis. CASE PRESENTATION In this report, we describe the case of a 33-year-old(More)
Case report 58-year-old man admitted to our hospital with axillary mass, night sweats, and weight loss. He had the history of 12 years of diabetes mellitus and smoking. Physical exam showed pallor, fever, and left axillary lymph node (5×6 cm). Lymph node biopsy from left axilla was reported as HL-nodular sclerosing type. PET/CT staging showed left(More)
Background/Objectives. Patients with myeloproliferative neoplasms have a well-established increased risk of thrombosis. Many trials report identification of an underlying myeloproliferative neoplasm by investigation of the patients developing portal hypertensive esophagus and/or fundus variceal hemorrhage in the absence of any known etiology. This trial was(More)
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