肉芽肿合并多血管炎累及垂体1例:报告并文献复习

Z. Habibagahi, Leila Azizi
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引用次数: 1

摘要

多血管炎肉芽肿病(Granulomatosis with polyangiitis, GPA),又称韦格纳氏病(Wegener 's),是一种抗中性粒细胞细胞质抗体相关的多系统疾病,以坏死性小血管炎为特征,主要累及上、下呼吸道和肾脏。累及中枢神经系统在GPA中并不常见,可能难以治疗。垂体受累是GPA的罕见表现。本文报告一位28岁女性,其GPA累及脑垂体及其他系统性表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pituitary involvement in a case of granulomatosis with polyangiitis: case report and literature review
Granulomatosis with polyangiitis ) GPA, also known as Wegener’s ( is an anti-neutrophil cytoplasmic antibody-associated multisystem disease characterized by necrotizing small vessel vasculitis which mainly affects the upper and lower respiratory tracts as well as the kidneys. Involvement of the central nervous system is uncommon in GPA and might be difficult to treat. Pituitary involvement is a rare presentation in GPA. Presented herein is the case of a 28-year-old woman with GPA involving the pituitary gland and other systemic manifestations of the disease.
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