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一位年轻女性的肉芽肿性多血管炎:实现缓解的挑战

Granulomatosis With Polyangiitis in a Young Lady: Challenges in Achieving Remission.

作者信息

Mohammad Nurul Ibtisam, Gunaseelan Shakiran, Kuganasan Sangeeta, Mat Saad Noram, Md Din Norshamsiah

机构信息

Ophthalmology, Universiti Kebangsaan Malaysia Medical Centre (UKMMC), Kuala Lumpur, MYS.

Ophthalmology, Hospital Tuanku Jaafar, Seremban, MYS.

出版信息

Cureus. 2024 Dec 5;16(12):e75139. doi: 10.7759/cureus.75139. eCollection 2024 Dec.

Abstract

Granulomatosis with polyangiitis (GPA) is a subtype of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) that commonly requires aggressive immunosuppression to achieve remission. We present a case of a young Malay lady with recurrent episodes of ANCA-positive nodular anterior scleritis who responded poorly to topical and systemic corticosteroids and relapsed while on methotrexate. A year later, she had epistaxis, and a sino-nasal biopsy confirmed granulomatous vasculitis. While receiving cyclophosphamide, she developed proptosis with optic neuropathy, which resolved with intravenous methylprednisolone. She eventually required rituximab as she was still having relapses on other immunosuppressants. Adequate and targeted treatment with immunomodulators is crucial to achieving disease remission in GPA.

摘要

肉芽肿性多血管炎(GPA)是抗中性粒细胞胞浆抗体(ANCA)相关血管炎(AAV)的一种亚型,通常需要积极的免疫抑制治疗以实现缓解。我们报告一例年轻马来女性病例,该患者反复出现ANCA阳性结节性前巩膜炎,局部和全身使用糖皮质激素治疗反应不佳,且在使用甲氨蝶呤期间复发。一年后,她出现鼻出血,鼻窦活检证实为肉芽肿性血管炎。在接受环磷酰胺治疗时,她出现眼球突出伴视神经病变,静脉注射甲泼尼龙后病情缓解。由于她在使用其他免疫抑制剂时仍有复发,最终需要使用利妥昔单抗。使用免疫调节剂进行充分且有针对性的治疗对于实现GPA疾病缓解至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b836/11699542/b301912e82f5/cureus-0016-00000075139-i01.jpg

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