Kogan E A, Grusha Ya O, Ismailova D S, Novikov P I, Abramova Yu V, Meshkov A D, Rizopulu E F
I.M. Sechenov First Moscow State Medical University, Moscow, Russia.
I.M. Sechenov First Moscow State Medical University, Moscow, Russia; Research Institute of Eye Diseases, Moscow, Russia.
Arkh Patol. 2017;79(1):56-60. doi: 10.17116/patol201779156-60.
Orbital granulomatosis with polyangiitis (Wegener's granulomatosis, GPA), which is characterized by granulomatous inflammation with small-vessel vasculitis, can develop in local and generalized forms of the disease. The introduction of current immunosuppressive therapy regimens has improved the prognosis of the disease; however, there are immunosuppressive treatment-refractory forms of GPA, the morphology of which has been inadequately investigated. The paper describes a clinical case of refractory GPA involving the orbit, as evidenced by histological and immunohistochemical examinations. The specific feature of the case is the development of severe fibrosis with the accumulation of mainly type III collagen and the persistence of granulomatous inflammation and productive-destructive vasculitis.
眼眶肉芽肿性多血管炎(韦格纳肉芽肿,GPA),其特征为伴有小血管血管炎的肉芽肿性炎症,可表现为疾病的局部和全身形式。目前免疫抑制治疗方案的引入改善了该病的预后;然而,存在免疫抑制治疗难治性的GPA形式,其形态学尚未得到充分研究。本文描述了一例经组织学和免疫组化检查证实的累及眼眶的难治性GPA临床病例。该病例的具体特征是出现严重纤维化,主要积聚III型胶原,同时存在肉芽肿性炎症和增殖性破坏性血管炎。