Jacobson I M, Kelsey P B, Blyden G T, Demirjian Z N, Isselbacher K J
Am J Gastroenterol. 1985 Feb;80(2):118-21.
We report a patient with ulcerative colitis in whom agranulocytosis was diagnosed 5 wk after the initiation of sulfasalazine therapy. Concomitant features included fever and skin rash, and bone marrow examination revealed severe myeloid hypoplasia. Antineutrophil antibodies were absent from the serum. Recovery began during the 2nd wk and was characterized by a leukemoid reaction with thrombocytosis. Subsequently, the patient received 5-aminosalicylate enemas without adverse effects. Agranulocytosis, a rare effect of sulfasalazine, appears to occur almost invariably during the first 2 months of therapy, and prompt evaluation is therefore required in patients with unexplained fever or other nonspecific illness during this period.
我们报告一例溃疡性结肠炎患者,在柳氮磺胺吡啶治疗开始5周后被诊断为粒细胞缺乏症。伴随症状包括发热和皮疹,骨髓检查显示严重的髓细胞发育不全。血清中不存在抗中性粒细胞抗体。在第2周开始恢复,其特征为类白血病反应伴血小板增多。随后,该患者接受5-氨基水杨酸灌肠,未出现不良反应。粒细胞缺乏症是柳氮磺胺吡啶的一种罕见不良反应,似乎几乎总是在治疗的前2个月内发生,因此在此期间出现不明原因发热或其他非特异性疾病的患者需要及时评估。