Bouchra Amine, Benbouazza Karima, Hajjaj-Hassouni Najia
Department of Rheumatology, El Ayachi Hospital, University Hospital of Rabat-Sale, 11000, Sale, Morocco.
Clin Rheumatol. 2009 Jun;28 Suppl 1:S53-5. doi: 10.1007/s10067-009-1154-7. Epub 2009 Mar 11.
We describe a 47-year-old woman with severe spondylarthropathy secondary to ulcerative colitis who developed a Guillain-Barre after the use of anti-TNF-alpha. She first developed ulcerative colitis in November 1997. In 2003, she developed uveitis and, in 2005, axial and enthesitis form of spondylarthropathy. In May 2007, her condition was exacerbated. Therapy with infliximab has been initiated. The patient received 5-mg/kg infusions of infliximab. She had significant improvement in her arthritis and was in remission for her ulcerative colitis. She was admitted to the hospital 2 weeks after her third dose of infliximab for having developed paraesthesia of her hands and lower limbs. Neurophysiology studies demonstrated an acquired segmental demyelinating polyneuropathy consistent with Guillain-Barre syndrome (GBS). Laboratory investigations were unremarkable. She was treated with intravenous corticosteroids with no improvement. After this, she received infusions of intravenous gammaglobulin (IVIg) with complete recovery of the muscle strength within a few weeks. A follow-up electromyographic study 3 months later showed normal finding. The development of GBS in our patient may be secondary to her anti-TNF-alpha treatment. At present, she remains off anti-TNF-alpha therapy.
我们描述了一名47岁患有继发于溃疡性结肠炎的严重脊柱关节病的女性,她在使用抗TNF-α后发生了吉兰-巴雷综合征。她于1997年11月首次患上溃疡性结肠炎。2003年,她出现了葡萄膜炎,2005年,出现了轴向和附着点炎形式的脊柱关节病。2007年5月,她的病情加重。开始使用英夫利昔单抗治疗。患者接受了5mg/kg的英夫利昔单抗输注。她的关节炎有显著改善,溃疡性结肠炎也处于缓解期。在第三次输注英夫利昔单抗两周后,她因出现双手和下肢感觉异常而入院。神经生理学研究显示为获得性节段性脱髓鞘性多发性神经病,符合吉兰-巴雷综合征(GBS)。实验室检查无异常。她接受了静脉注射皮质类固醇治疗,但没有改善。此后,她接受了静脉注射免疫球蛋白(IVIg)输注,几周内肌肉力量完全恢复。3个月后的随访肌电图检查结果正常。我们患者发生GBS可能继发于她的抗TNF-α治疗。目前,她仍未接受抗TNF-α治疗。