Nichols J C, Ince A, Akduman L, Mann E S
Saint Louis University Eye Institute, Missouri 63104, USA.
J Neuroophthalmol. 2001 Jun;21(2):109-11. doi: 10.1097/00041327-200106000-00011.
Behcet disease is a multisystemic, chronic, recurrent inflammatory disorder characterized as a triad of hypopyon uveitis, oral aphthae, and genital ulcers. Neurologic involvement in Behcet disease (neuro-Behcet) is common. Neuro-Behcet disease typically manifests late after disease onset, rarely coincides with ocular involvement, and often heralds a poor prognosis for final vision and survival. We present a case of neuro-Behcet disease with neurologic onset concomitant with systemic and ocular involvement that was responsive to treatment with interferon-alpha 2a.
白塞病是一种多系统、慢性、复发性炎症性疾病,其特征为前房积脓性葡萄膜炎、口腔溃疡和生殖器溃疡三联征。白塞病的神经系统受累(神经白塞病)很常见。神经白塞病通常在疾病发作后较晚出现,很少与眼部受累同时发生,并且常常预示着最终视力和生存率不佳。我们报告一例以神经系统症状起病,同时伴有全身和眼部受累的神经白塞病病例,该病例对α-2a干扰素治疗有反应。