Schoonjans R, Mast A, Van den Abeele G, Dewilde D, Achten E, Van Maele V, Pauwels W
Department of Gastroenterology, Algemene Kliniek H. Familie, Ghent, Belgium.
Am J Gastroenterol. 1993 Oct;88(10):1759-63.
We report a case of acute encephalopathy in a patient with Crohn's disease who had taken sulfasalazine for 1 month. The development of toxic hepatitis and dermatitis prompted interruption of the drug. Four days later, neurologic symptoms became evident. These included acute monoparesis of the left arm, the development of stupor and coma, with endorotation of both arms, and a left Babinski sign. CT and MR imaging revealed multiple lesions in the white and gray brain matter, suggesting diffuse cerebral microangiitis. All cerebrospinal fluid examinations were negative. Methylprednisolone was given intravenously. Complete clinical normalization followed. Neurotoxicity secondary to sulfasalazine has seldom been reported in the literature. We found certain similarities with two previous case reports suggesting a hypersensitivity reaction to sulfasalazine or one of its metabolites. For ethical reasons, no rechallenge was performed.
我们报告一例克罗恩病患者服用柳氮磺胺吡啶1个月后出现急性脑病的病例。毒性肝炎和皮炎的出现促使停药。4天后,神经症状变得明显。这些症状包括左臂急性单瘫、昏迷和木僵的发展,双臂内旋,以及左侧巴宾斯基征。CT和磁共振成像显示脑白质和灰质有多个病变,提示弥漫性脑微血管炎。所有脑脊液检查均为阴性。静脉注射甲泼尼龙。随后临床完全恢复正常。柳氮磺胺吡啶继发的神经毒性在文献中鲜有报道。我们发现与之前的两例病例报告有某些相似之处,提示对柳氮磺胺吡啶或其一种代谢产物过敏反应。出于伦理原因,未进行再次激发试验。