Megadose methylprednisolone for Evans syndrome.
نویسنده
چکیده
I was pleased to read Berber et al’s 50 year-old patient with Evans syndrome which was published as a Letter to The Editor in the recent issue of the Journal of Turgut Ozal Medical Center (2013;20(3):289-290). But, it was surprised to me that mega dose methyl prednisolone (MDMP) treatment was not brought to attention which had been successfully used for these patients first time from our country (1,2). Although it is a type corticosteroid administration treatment, it differs by its dosage (initially 30-100 mg/kg/day), the time of administration (around 6 a.m) (orally at once, intravenously 10-15 minutes) from conventional (1-2 mg/kg) uses divided doses, pulse methyl prednisolone (1000 mg given within 4 hours any time of the day, local injections intraocularly or by inhalation. MDMP administration is not only more effective, but also has less side effects (3,4). IVIG is not only very expensive, but also potentially harmful (5).
منابع مشابه
Megadose Methylprednisolone (MDMP) Treatment in a Patient with Autoimmune Hemolytic Anemia (AIHA) Resistant to Conventional Corticosteroid Administration: A Case Report
UNLABELLED A female in the Netherlands with severe autoimmune hemolytic anemia (AIHA) was treated with conventional corticosteroid (2 mg/kg/d in divided doses) and blood transfusions for 18 months without improvement. The presented patient responded to megadose methylprednisolone (MDMP) 30 mg/kg/d for 3 d, followed by 20 mg/kg for 4 d, and subsequently 10, 5, 2, and 1 mg/kg/d each for 1 week. ...
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Redundant studies proved coronavirus infection results from a defect in a suitable immune response that may exacerbate immune-inflammatory reactions like cytokine storm and autoimmunity. Evans syndrome (ES) is a rare chronic autoimmune disease that distinguishes it from autoimmune hemolytic anemia (AIHA) and immune thrombocytopenic purpura (ITP). Reports have shown significant differences in im...
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Background: Evans syndrome is an uncommon autoimmune disorder manifested by fatigue, jaundice, pallor, purpura and petechiae. The main characteristics of this rare disease are simultaneous or sequential existence of positive anti-globulin test, immune thrombocytopenia (ITP) and autoimmune hemolytic anemia (AIHA). Evans syndrome as an autoimmune disorder can be associated with other diseases. Th...
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ورودعنوان ژورنال:
- Pediatric hematology and oncology
دوره 17 8 شماره
صفحات -
تاریخ انتشار 2000