Division of Rheumatology, Department of Medicine, New York University School of Medicine, New York, NY, United States.
Department of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD, United States.
Autoimmun Rev. 2017 Sep;16(9):980-983. doi: 10.1016/j.autrev.2017.07.013. Epub 2017 Jul 12.
While the relationship between maternal connective tissue diseases and neonatal rashes was described in the 1960s and congenital heart block in the 1970s, the "culprit" antibody reactivity to the SSA/Ro-SSB/La ribonucleoprotein complex was not identified until the 1980s. However, studies have shown that approximately 10-15% of cases of congenital heart block are not exposed to anti-SSA/Ro-SSB/La. Whether those cases represent a different disease entity or whether another antibody is associated has yet to be determined. Moreover, the cutaneous manifestations of neonatal lupus have also been identified in infants exposed only to anti-U1RNP antibodies. In this review, we describe what we believe to be the first case of congenital heart block exposed to maternal anti-U1RNP antibodies absent anti-SSA/Ro-SSB/La. The clinical and pathologic characteristics of this fetus are compared to those typically seen associated with SSA/Ro and SSB/La. Current guidelines for fetal surveillance are reviewed and the potential impact conferred by this case is evaluated.
虽然在 20 世纪 60 年代就描述了母体结缔组织疾病与新生儿皮疹之间的关系,在 20 世纪 70 年代就描述了先天性心脏传导阻滞,但直到 20 世纪 80 年代才确定了“罪魁祸首”抗体对 SSA/Ro-SSB/La 核糖核蛋白复合物的反应性。然而,研究表明,大约有 10-15%的先天性心脏传导阻滞病例没有接触到抗 SSA/Ro-SSB/La。这些病例是否代表不同的疾病实体,或者是否与其他抗体相关,还有待确定。此外,仅暴露于抗 U1RNP 抗体的婴儿也出现了新生儿狼疮的皮肤表现。在这篇综述中,我们描述了我们认为首例接触母体抗 U1RNP 抗体而不存在抗 SSA/Ro-SSB/La 的先天性心脏传导阻滞病例。该胎儿的临床和病理特征与通常与 SSA/Ro 和 SSB/La 相关的特征进行了比较。回顾了胎儿监测的现行指南,并评估了该病例带来的潜在影响。