Lalezari P, Khorshidi M, Petrosova M
J Pediatr. 1986 Nov;109(5):764-9. doi: 10.1016/s0022-3476(86)80690-4.
Neutrophil antibodies were demonstrated in 119 of 121 infants and young children with chronic neutropenia, establishing the diagnosis of autoimmune neutropenia of infancy. The median age at diagnosis was 8 months (range 3 to 30 months), and the female/male ratio was 6:4. Autoimmune neutropenia of infancy was manifested by recurrent fever and infection. All patients had selective neutropenia (absolute neutrophil count 0 to 500), and many had monocytosis. Fifteen of 16 patients tested failed to respond to epinephrine and hydrocortisone stimulation. Bone marrow had myeloid hyperplasia and reduced mature neutrophils. Recovery occurred in all 81 patients who passed the age of 5 years, except for one patient who is recovering at 6 1/2 years. The median age at recovery was 30 months; 95% recovered before 4 years. The estimated median duration of disease was 20 months. Neutrophil antibodies were detected early in the neutropenic phase by a combination of immunofluorescence and agglutination tests. Ten percent of these antibodies had specificity for NA1 or NA2. Ten of the 12 serum samples with a strong reaction in the flow cytometer reacted only with neutrophils. Two also reacted with an unidentified subpopulation (30%) of lymphocytes. Lymphocyte subsets were normal in 10 patients investigated, and abnormal levels of circulating immune complexes were detected in sera from 11 of 25 (44%) patients tested. Temporary remission was induced in all of eight patients who received intravenous IgG therapy. Autoimmune neutropenia of infancy is probably the most common cause of chronic neutropenia in infancy and early childhood, can be diagnosed by immunologic techniques, and requires only conservative management; spontaneous cure appears to be the rule.
在121例患有慢性中性粒细胞减少症的婴幼儿中,119例检测到中性粒细胞抗体,从而确诊为婴儿自身免疫性中性粒细胞减少症。诊断时的中位年龄为8个月(范围3至30个月),女性/男性比例为6:4。婴儿自身免疫性中性粒细胞减少症表现为反复发热和感染。所有患者均有选择性中性粒细胞减少(绝对中性粒细胞计数为0至500),许多患者还有单核细胞增多。16例接受检测的患者中有15例对肾上腺素和氢化可的松刺激无反应。骨髓有髓样增生且成熟中性粒细胞减少。所有81例超过5岁的患者均康复,除1例在6岁半时仍在康复中。康复的中位年龄为30个月;95%的患者在4岁前康复。疾病的估计中位持续时间为20个月。在中性粒细胞减少期早期,通过免疫荧光和凝集试验相结合的方法检测到中性粒细胞抗体。这些抗体中有10%对NA1或NA2具有特异性。在流式细胞仪中反应强烈的12份血清样本中,有10份仅与中性粒细胞反应。另外两份还与未识别的淋巴细胞亚群(30%)反应。在10例接受调查的患者中,淋巴细胞亚群正常,在25例接受检测的患者中,有11例(44%)的血清中检测到循环免疫复合物水平异常。所有8例接受静脉注射免疫球蛋白治疗的患者均诱导出暂时缓解。婴儿自身免疫性中性粒细胞减少症可能是婴幼儿期慢性中性粒细胞减少症最常见的原因,可通过免疫技术诊断,仅需保守治疗;似乎通常会自发治愈。