Conway L T, Clay M E, Kline W E, Ramsay N K, Krivit W, McCullough J
Pediatrics. 1987 May;79(5):728-33.
Five patients with primary autoimmune neutropenia were evaluated during their first 2 years of life. Their illness resolved spontaneously after 6 to 41 months (median 13 months), and the patients were subsequently followed for 13 to 73 months (median 28 months). None required immunosuppressive therapy to induce remission, and routine antibiotic therapy adequately controlled all infectious episodes. An increased rate of infection, particularly otitis media and upper respiratory tract infection, occurred during the neutropenic period. No other noninfectious illnesses, particularly no other autoimmune diseases, were reported in any of these patients at any time. In each case, resolution of neutropenia paralleled the disappearance of neutrophil autoantibodies which were specific for the NA1 antigen. This report describes the clinical and laboratory findings and the long-term history of primary autoimmune neutropenia in these five patients.
对5例原发性自身免疫性中性粒细胞减少症患者在其出生后的头2年进行了评估。他们的病情在6至41个月(中位数13个月)后自发缓解,随后对这些患者进行了13至73个月(中位数28个月)的随访。无人需要免疫抑制治疗来诱导缓解,常规抗生素治疗充分控制了所有感染发作。在中性粒细胞减少期,感染率增加,尤其是中耳炎和上呼吸道感染。在这些患者中的任何时候均未报告其他非感染性疾病,特别是未报告其他自身免疫性疾病。在每种情况下,中性粒细胞减少症的缓解与针对NA1抗原的中性粒细胞自身抗体的消失同时发生。本报告描述了这5例患者原发性自身免疫性中性粒细胞减少症的临床和实验室检查结果以及长期病史。