Miller B A, Schultz Beardsley D
J Pediatr. 1983 Dec;103(6):877-81. doi: 10.1016/s0022-3476(83)80705-7.
Five patients with immune thrombocytopenia and neutropenia, including three with autoimmune hemolytic anemia, are described; none had identifiable underlying disease. All patients had demonstrable autoantibodies against multiple hematopoietic cell types, and in two patients, the antiplatelet and antierythrocyte antibodies were shown to be distinct. All patients had continuing disease, and with follow-up of 2 to 6 1/2 years, all developed nonhematologic disease manifestations. These patients demonstrate that even in the absence of identifiable underlying disease, autoimmune hematologic disease resulting from production of antibodies against red cells, white cells, and platelets often involves a generalized disorder of immune regulation, with multisystem disease manifestations and a prolonged course.
本文描述了5例免疫性血小板减少症和中性粒细胞减少症患者,其中3例伴有自身免疫性溶血性贫血;均未发现潜在疾病。所有患者均有针对多种造血细胞类型的可证实的自身抗体,且在2例患者中,抗血小板和抗红细胞抗体显示为不同抗体。所有患者病情持续,经过2至6.5年的随访,均出现了非血液系统疾病表现。这些患者表明,即使在没有可识别的潜在疾病的情况下,由针对红细胞、白细胞和血小板产生抗体导致的自身免疫性血液疾病通常涉及免疫调节的全身性紊乱,伴有多系统疾病表现和病程延长。