043 AKI & HEPATITIS C: A CASE OF CO-EXISTING ANTIPHOSPHOLIPID SYNDROME & MIXED CRYOGLOBULINEMIA

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Hepatitis C Virus Infection and Mixed Cryoglobulinemia

Hepatitis C virus (HCV) chronic infection is recognized as the major cause of mixed cryoglobulinemia (MC). Its persistence represents a continuous stimulus for host immune system with production of circulating immune complexes (ICs), one-third of them with cryoprecipitate property. Several factors contribute to the biological activities of ICs, many of which are not completely known. Among them...

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Mixed cryoglobulinemia: an unusual presentation of hepatitis C.

A 50-year-old man with a history of hepatitis C presented with recurrent episodes of abdominal pain, arthralgia, and weakness. Although these symptoms seemed rather non-specific, a purpuric rash of the lower extremities was the final clue to diagnosis. The diagnosis was then confirmed by histopathologic and serologic testing.

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Type III Mixed Cryoglobulinemia and Antiphospholipid Syndrome in a Patient With Partial DiGeorge Syndrome

We studied a 14 year-old boy with partial DiGeorge syndrome (DGS), status post complete repair of Tetralogy of Fallot, who developed antiphospholipid syndrome (APS) and type III mixed cryoglobulinemia. He presented with recurrent fever and dyspnea upon exertion secondary to right pulmonary embolus on chest computed tomography (CT). Coagulation studies revealed homozygous methylene tetrahydrofol...

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Cryoglobulinemia in patients with hepatitis C

Introduction: Cryoglobulinemia is a kind of immunoglobuline that form in various conditions. These imunoglobulines, precipitate in cold environment and restore to soluble state upon rewarming. Nowadays, strong association between cryoglobulines and hepatitis C has been proposed. Methods: This is a descriptive-analytic study in which we included all documented cases of hepatitis C infection wh...

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Thyroid involvement in hepatitis C - associated mixed cryoglobulinemia.

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ژورنال

عنوان ژورنال: Kidney International Reports

سال: 2017

ISSN: 2468-0249

DOI: 10.1016/j.ekir.2017.06.092