Evans syndrome is an autoimmune disorder described by Robert in 1951 specifying that a link exists between primary thrombocytopenic purpura and acquired haemolytic anaemia. It rare characterised the simultaneous or sequential development of anaemia (AIHA) immune thrombocytopenia (ITP) with without neutropenia. Approximately, represent 5-10% warm cases 2-5% ITP cases. basically diagnosis exclusi...

Acute hemorrhagic edema of infancy (AHEI) is a rare skin disorder which was first described by Snow in 1913. Clinical manifestations are usually limited to cutaneous lesions and is most commonly observed in infants under the age of 1 year. Usually, there is a history of recent upper respiratory tract infection and antibiotic administration. Clinical presentation of this disease includes petechi...

A 48 Year-old woman had symptoms of thyrotoxicosis which disappeared spontaneously within two months. She was diagnosed as case of silent thyroiditis on the basis of both the clinical course and the laboratory data such as low uptake of radioactive Iodine and Technesium. She also had petechia in her arms which were diagnosed as an idiopathic thrombocytopenic purpura (I.T.P.). This case would se...

Right-sided endocarditis is exceptional in non-drug addict patients without previous heart disease. Few cases have been published, and its diagnosis sometimes presents a significant clinical challenge. We describe a 57-year-old patient with no history of parenteral drug addiction or vascular catheter use, who had tricuspid valve endocarditis in a morphologically normal valve. The clinical debut...

Leukemia is the most common neoplastic disease of the white blood cells which is important as a pediatric malignancy. Oral manifestations occur frequently in leukemic patients and may present as initial evidence of the disease or its relapse. The symptoms include gingival enlargement and bleeding, oral ulceration, petechia, mucosal pallor, noma, trismus and oral infections. Oral lesions arise i...

The clinical findings of 29 patients with hemorrhagic fever with renal syndrome (HFRS) caused by Seoul virus were evaluated and compared with the previously reported clinical findings of classic Korean hemorrhagic fever (KHF). The diagnoses of these patients were made by hemagglutination inhibition test. The results were as follows: 1) The disease occurred predominantly in males with a high inc...

BACKGROUND We aimed to examine cases of brucellosis that presented with severe thrombocytopenia and hemorrhagic diathesis. METHODS A total of 10 brucellosis cases with severe thrombocytopenia were included in this case-series study. Patients' files were reviewed for their clinical and laboratory findings, as well as clinical outcomes and complications. Platelet counts of < 20,000/mm³ were dia...