Giant cell arteritis with myeloperoxidase anti-neutrophil cytoplasmic antibody seropositivity in a patient with systemic sclerosis.

Yoshihiro Kitahara, Rie Nakamura, Makiko Kawai, Tetsu Hirakawa, Arisa Hamada, Mineyo Mito, Kikuo Nakano
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Abstract

To the best of our knowledge, systemic sclerosis with overlapping characteristics of both microscopic polyangiitis and giant cell arteritis (i.e. microscopic polyangiitis involving the superficial temporal artery or giant cell arteritis with myeloperoxidase anti-neutrophil cytoplasmic antibody seropositivity) has not been reported previously. An 82-year-old woman with diffuse cutaneous systemic sclerosis experienced dyspnoea on exertion and fever. No signs of infection were observed on computed tomography. Her fever persisted despite antibiotic treatment for occult bacterial infection and secondary Clostridioides difficile-associated diarrhoea. Microscopic polyangiitis was suspected because of myeloperoxidase anti-neutrophil cytoplasmic antibody seropositivity, and giant cell arteritis was suspected as a differential diagnosis due to swelling of the superficial temporal artery. Arterial biopsy revealed inflammatory cell infiltration with granuloma formation. Based on the presence of granulomatous inflammation in the superficial temporal artery, we concluded that giant cell arteritis with myeloperoxidase anti-neutrophil cytoplasmic antibody seropositivity occurred as a complication. After glucocorticoid therapy, her fever and dyspnoea on exertion improved with a gradual decline in the serum myeloperoxidase anti-neutrophil cytoplasmic antibody levels. It is possible that vasculitis occurs as a complication in patients with systemic sclerosis in cases where the fever persists and cannot be explained by systemic sclerosis itself, infectious disease, or malignancy. Clinicians must be careful not to prematurely diagnose microscopic polyangiitis based on myeloperoxidase anti-neutrophil cytoplasmic antibody seropositivity or giant cell arteritis based on the swelling of the superficial temporal artery. Careful evaluation of the presence of granulomatous inflammation in an arterial biopsy specimen is essential to differentiate between microscopic polyangiitis and giant cell arteritis.

系统性硬化症巨细胞动脉炎伴髓过氧化物酶抗中性粒细胞胞浆抗体血清阳性1例。
据我们所知,显微镜下多血管炎和巨细胞动脉炎重叠特征的系统性硬化症(即显微镜下多血管炎累及颞浅动脉或巨细胞动脉炎伴髓过氧化物酶抗中性粒细胞细胞质抗体血清阳性)以前未见报道。一名82岁女性弥漫性皮肤系统性硬化症患者在劳累和发烧时出现呼吸困难。计算机断层扫描未见感染迹象。尽管对隐匿性细菌感染和继发性难辨梭状芽胞杆菌相关腹泻进行了抗生素治疗,但她仍在发烧。显微镜下多血管炎因髓过氧化物酶抗中性粒细胞细胞质抗体血清阳性而被怀疑,巨细胞动脉炎因颞浅动脉肿胀而被怀疑为鉴别诊断。动脉活检显示炎性细胞浸润伴肉芽肿形成。基于颞浅动脉肉芽肿性炎症的存在,我们得出结论,巨细胞动脉炎伴髓过氧化物酶抗中性粒细胞细胞质抗体血清阳性作为并发症发生。经糖皮质激素治疗后,患者发热和运动时呼吸困难改善,血清髓过氧化物酶抗中性粒细胞胞浆抗体水平逐渐下降。血管炎有可能作为系统性硬化症患者的并发症发生,在发烧持续的情况下,不能用系统性硬化症本身、传染病或恶性肿瘤来解释。临床医生必须小心,不要过早诊断基于髓过氧化物酶抗中性粒细胞细胞质抗体血清阳性的显微镜下多血管炎或基于颞浅动脉肿胀的巨细胞动脉炎。仔细评估动脉活检标本中肉芽肿性炎症的存在是区分显微镜下多血管炎和巨细胞动脉炎的必要条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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