Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Lupus. 2011 Apr;20(5):527-30. doi: 10.1177/0961203310384122. Epub 2010 Dec 10.
We report a case of a 3-month old male infant, born to a mother with a known history of systemic lupus erythematosus (SLE). The infant initially presented with petechiae, anemia, and thrombocytopenia. His evaluation revealed antinuclear antibody (ANA) titer of 1 : 160, negative anti-SS-A/SS-B antibody, positive anti-Smith antibody, elevated anti-dsDNA titer, and a slightly low C4 level. His subsequent development of hematuria with nephrotic grade proteinuria fulfilled criteria for a diagnosis of SLE. His condition improved with corticosteroids, mycophenolate mofetil and low-dose aspirin. At 18 months of age, he is clinically well, off all immunosuppression with normal growth parameters and no detectable autoantibodies.
我们报告了一例 3 个月大的男性婴儿,其母亲患有系统性红斑狼疮(SLE)。该婴儿最初表现为瘀点、贫血和血小板减少症。他的评估显示抗核抗体(ANA)滴度为 1:160,抗-SS-A/SS-B 抗体阴性,抗-Smith 抗体阳性,抗双链 DNA 滴度升高,C4 水平略低。他随后出现血尿和肾病级蛋白尿,符合 SLE 的诊断标准。他的病情在皮质类固醇、霉酚酸酯和低剂量阿司匹林的治疗下得到改善。在 18 个月大时,他临床状况良好,已停用所有免疫抑制剂,生长参数正常,且未检测到自身抗体。