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血管炎性周边溃疡性角膜炎

Vasculitic peripheral ulcerative keratitis.

作者信息

Messmer E M, Foster C S

机构信息

University Eye Hospital, Munich, Germany.

出版信息

Surv Ophthalmol. 1999 Mar-Apr;43(5):379-96. doi: 10.1016/s0039-6257(98)00051-4.

Abstract

The onset of peripheral ulcerative keratitis in the course of a connective tissue disorder, such as rheumatoid arthritis, relapsing polychondritis, or systemic lupus erythematosus, may reflect the presence of potentially lethal systemic vasculitis. Moreover, peripheral ulcerative keratitis may be the first sign of systemic necrotizing vasculitis in patients with Wegener's granulomatosis, polyarteritis nodosa, microscopic polyangiitis, or Churg-Strauss syndrome. Although the exact pathogenesis of this severe corneal inflammation and destruction is not well understood, evidence points to a dysfunction in immunoregulation with immune complexes formed in response to autoantigens or to some unknown microbial antigen depositing in scleral and limbal vessels. These events lead to changes that are mainly responsible for the resulting tissue damage. In pauci-immune vasculitides positive for antineutrophil cytoplasmic antibodies, cell-mediated cytotoxicity may play an important role in the pathogenesis of peripheral ulcerative keratitis. Untreated systemic conditions such as those mentioned above may carry a grave prognosis for the eye and may also be life-threatening. Immunosuppressive therapy with corticosteroids and cytotoxic agents is, we believe, mandatory in the treatment of these multisystem disorders associated with vasculitic peripheral ulcerative keratitis.

摘要

在结缔组织疾病(如类风湿性关节炎、复发性多软骨炎或系统性红斑狼疮)病程中出现的周边溃疡性角膜炎,可能提示存在潜在致命性的系统性血管炎。此外,周边溃疡性角膜炎可能是韦格纳肉芽肿病、结节性多动脉炎、显微镜下多血管炎或变应性肉芽肿性血管炎患者系统性坏死性血管炎的首发症状。尽管这种严重角膜炎症和破坏的确切发病机制尚不完全清楚,但有证据表明免疫调节功能障碍,即针对自身抗原或沉积在巩膜和角膜缘血管中的某些未知微生物抗原形成免疫复合物。这些事件导致的变化是造成组织损伤的主要原因。在抗中性粒细胞胞浆抗体阳性的寡免疫性血管炎中,细胞介导的细胞毒性可能在周边溃疡性角膜炎的发病机制中起重要作用。上述未治疗的全身性疾病可能对眼睛预后严重,也可能危及生命。我们认为,使用皮质类固醇和细胞毒性药物进行免疫抑制治疗对于这些与血管炎性周边溃疡性角膜炎相关的多系统疾病的治疗是必不可少的。

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