Ebrahimiadib Nazanin, Modjtahedi Bobeck S, Roohipoor Ramak, Anesi Stephen D, Foster C Stephen
*Massachusetts Eye Research and Surgery Institution, Waltham, MA; †Ocular Immunology and Uveitis Foundation, Waltham, MA; ‡Massachusetts Eye and Ear Infirmary, Boston, MA; §Eye Research Center, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran, Iran; and ¶Department of Ophthalmology, Harvard Medical School, Boston, MA.
Cornea. 2016 Nov;35(11):1459-1465. doi: 10.1097/ICO.0000000000000919.
Management of granulomatosis with polyangiitis (GPA)-associated peripheral ulcerative keratitis (PUK) is challenging and lacks definite guidelines. We aimed to summarize our treatment and outcome experience with patients with GPA-PUK.
The Massachusetts Eye Research and Surgery Institution patient database was searched from 2005 to 2015 to identify patients with diagnosis of PUK who suffered from GPA. Individual patient histories were examined, and treatment strategies and outcomes were summarized.
There were 16 patients who started treatment with a mean duration follow-up of 64 months (range: 12-110 mo). Rituximab and cyclophosphamide, either alone or in combination with other agents, were the most successful agents in controlling inflammation. Rituximab was administered in 11 patients with remission being achieved in all. Cyclophosphamide successfully controlled inflammation in 50% (5/10). Two of the patients (2/5, 40%) who had achieved initial control on cyclophosphamide had flares of their PUK. Two of 11 (18%) patients on rituximab had flares of scleritis and orbital inflammation but not PUK. Two patients, one in each treatment group, stopped treatment after achieving remission after 6 months of therapy but suffered disease recurrence within 2 months of treatment cessation.
Rituximab achieved a high rate of disease control in PUK patients with GPA and is the preferred agent in halting disease progression.
肉芽肿性多血管炎(GPA)相关的周边溃疡性角膜炎(PUK)的管理具有挑战性且缺乏明确的指南。我们旨在总结我们对GPA-PUK患者的治疗及预后经验。
检索2005年至2015年马萨诸塞州眼研究与手术机构的患者数据库,以识别诊断为PUK且患有GPA的患者。检查个体患者病史,并总结治疗策略及预后情况。
有16例患者开始接受治疗,平均随访时间为64个月(范围:12 - 110个月)。利妥昔单抗和环磷酰胺,单独使用或与其他药物联合使用,是控制炎症最成功的药物。11例患者使用了利妥昔单抗,全部实现缓解。环磷酰胺成功控制炎症的比例为50%(5/10)。在环磷酰胺治疗中最初病情得到控制的患者中有2例(2/5,40%)出现PUK复发。使用利妥昔单抗治疗的11例患者中有2例(18%)出现巩膜炎和眼眶炎症复发,但未出现PUK复发。2例患者,每个治疗组各1例,在6个月治疗缓解后停止治疗,但在停药后2个月内疾病复发。
利妥昔单抗在GPA的PUK患者中实现了较高的疾病控制率,是阻止疾病进展的首选药物。