Granulocyte-colony-stimulating Factor-resistant Neutropenia and Polyneuropathy Presenting as Severe Complications of Sjögren's Syndrome.

Katsuyuki Tomita, Shinnosuke Tokugawa, Genki Inui, Shotaro Moriyasu, Tomoyuki Ikeuchi, Hirokazu Touge, Fuminari Tajima
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Abstract

Primary Sjögren's syndrome (pSS) has multi-dimensional manifestations, including neutropenia and polyneuropathy. We herein report a 76-year-old woman with pSS initially presenting as severe granulocyte-colony-stimulating factor (G-CSF)-refractory neutropenia and axonal sensorimotor polyneuropathies (SMP). Systemic glucocorticoid administration had reduced neutrophil-associated immunoglobulin G (NAIgG) on the neutrophil surface as detected using flow cytometry, resulting in the development of neutropenia. A patient with pSS concomitant with axonal SMP might show severe neutropenia as aggressive autoimmune disease. Neutropenia can be treated with systemic glucocorticoids based on the assessment of NAIgG on the neutrophil surface.

粒细胞集落刺激因子抵抗性中性粒细胞减少症和多发性神经病表现为Sjögren综合征的严重并发症
原发性Sjögren综合征(pSS)具有多方面的表现,包括中性粒细胞减少和多神经病变。我们在此报告一位76岁的女性pSS患者,最初表现为严重的粒细胞集落刺激因子(G-CSF)难治性中性粒细胞减少症和轴突感觉运动多发性神经病(SMP)。流式细胞术检测,全身糖皮质激素使中性粒细胞表面的中性粒细胞相关免疫球蛋白G (NAIgG)减少,导致中性粒细胞减少症的发生。pSS合并轴突性SMP的患者可能表现为严重的中性粒细胞减少症,作为侵袭性自身免疫性疾病。中性粒细胞减少症可根据中性粒细胞表面NAIgG的评估,用全身糖皮质激素治疗。
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