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The Journal of the Korean Rheumatism Association ; : 231-234, 2005.
Article in Korean | WPRIM | ID: wpr-117064

ABSTRACT

Sulfasalazine produces a varied spectrum of adverse reactions on the hematopoietic system. Sulfasalazine-induced megaloblastic anemia is very rare and a few cases have been reported in patients with inflammatory bowel disease. Most of them show a low serum folate level. The pathogenesis is known as folate deficiency by intestinal folate malabsorption, inhibition of folate enzyme, or hemolysis. We experienced a 43-year old female with Behcet's disease, who presented with megaloblastic anemia having normal serum folate level after treatement of sulfasalazine (2 g/day for 3 months). Megaloblastic anemia recovered after withdrawal of the drug only.


Subject(s)
Adult , Female , Humans , Anemia, Megaloblastic , Folic Acid , Hematopoietic System , Hemolysis , Inflammatory Bowel Diseases , Megaloblasts , Sulfasalazine
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