Lee Lela A
Denver Health Medical Center, Denver, CO 80204, USA.
Paediatr Drugs. 2004;6(2):71-8. doi: 10.2165/00148581-200406020-00001.
Neonatal lupus is an uncommon autoimmune disease manifested primarily by cutaneous lupus lesions and/or congenital heart block. Maternal autoantibodies of the Ro/La family are present in virtually every case, although only approximately 1% of women who have these autoantibodies will have a baby with neonatal lupus. The cutaneous lesions of neonatal lupus may be present at birth, but more often develop within the first few weeks of life. Lesions are most common on the face and scalp, often in a distinctive periorbital distribution. Lesions tend to resolve in a few weeks or months without scarring. The most common cardiac manifestation of neonatal lupus is complete heart block. Heart block typically begins in utero during the second or third trimester. In some cases, heart block begins as first- or second-degree block and then progresses to third-degree block. Complete heart block, once established, appears to be irreversible. In some cases, cardiomyopathy occurs together with complete heart block. Most cases have been noted at birth, but delayed dilated cardiomyopathy has been reported. There have been a few cases of endocardial fibroelastosis occurring in the absence of congenital heart block. Hepatobiliary disease occurs in about 10% of cases. Three types of hepatobiliary disease have been observed: liver failure occurring at birth or in utero, transient conjugated hyperbilirubinemia occurring in infants, or transient transaminase elevations occurring in infants. Hematologic disease, consisting of thrombocytopenia, neutropenia, or anemia, occurs in about 10% of cases. It is common for children with neonatal lupus not to have the full expression of disease, but rather to have only one or two organ systems involved. The diagnosis rests largely on the finding of compatible clinical manifestations plus maternal autoantibodies to Ro and/or La, or, in a few cases, to U1 ribonuclear protein. Although the pathogenesis has not been conclusively established, accumulating evidence, including evidence from animal models, implicates autoantibodies in the pathogenesis of the disease. Therapeutic interventions include attempts at prevention, early intervention, and treatment of well established disease, mainly through the use of systemic corticosteroids. Optimal therapy has yet to be determined. The long-term prognosis for children who have had neonatal lupus is still under investigation, but some children who had neonatal lupus have developed other autoimmune diseases later in childhood. About half of the mothers are asymptomatic at the time of presentation of the child, but some of these women eventually develop symptoms of autoimmune disease.
新生儿红斑狼疮是一种罕见的自身免疫性疾病,主要表现为皮肤红斑狼疮损害和/或先天性心脏传导阻滞。几乎每例患儿体内都存在Ro/La家族的母体自身抗体,不过在有这些自身抗体的女性中,仅有约1%的女性会生下患新生儿红斑狼疮的婴儿。新生儿红斑狼疮的皮肤损害在出生时可能就已存在,但更常见于出生后的头几周内出现。损害最常见于面部和头皮,常呈独特的眶周分布。损害往往在几周或数月内消退,不留瘢痕。新生儿红斑狼疮最常见的心脏表现是完全性心脏传导阻滞。心脏传导阻滞通常在妊娠中期或晚期于子宫内开始。在某些情况下,心脏传导阻滞起初为一度或二度阻滞,随后进展为三度阻滞。一旦出现完全性心脏传导阻滞,似乎是不可逆的。在某些情况下,心肌病与完全性心脏传导阻滞同时发生。大多数病例在出生时就已被发现,但也有迟发性扩张型心肌病的报道。有少数病例在无先天性心脏传导阻滞的情况下发生心内膜弹力纤维增生症。约10%的病例会出现肝胆疾病。已观察到三种类型的肝胆疾病:出生时或子宫内发生的肝功能衰竭、婴儿期出现的短暂性结合胆红素血症或婴儿期出现的短暂性转氨酶升高。血液系统疾病,包括血小板减少症、中性粒细胞减少症或贫血,约在10%的病例中出现。患新生儿红斑狼疮的儿童通常不会出现疾病的全部表现,而往往仅累及一两个器官系统。诊断主要依据发现符合的临床表现以及母体针对Ro和/或La的自身抗体,或在少数情况下,针对U1核糖核蛋白的自身抗体。尽管发病机制尚未最终明确,但越来越多的证据,包括来自动物模型的证据,表明自身抗体在该疾病的发病机制中起作用。治疗干预措施包括预防尝试、早期干预以及对已确诊疾病的治疗,主要通过使用全身性皮质类固醇。最佳治疗方案尚未确定。患过新生儿红斑狼疮的儿童的长期预后仍在研究中,但一些患过新生儿红斑狼疮的儿童在童年后期患上了其他自身免疫性疾病。约一半的母亲在孩子患病时无症状,但其中一些女性最终会出现自身免疫性疾病的症状。