Ali U S, Dalvi R B, Merchant R H, Mehta K P, Chablani A T, Badakere S S, Bhatia H M
Indian Pediatr. 1989 Sep;26(9):868-73.
Twenty cases of systemic lupus erythematosus (SLE) in prepubertal children (less than 14 years of age) were seen over a period of 14 years. The male:female ratio was 1:2.3, and the mean age at onset was 9.37 years. Fever with joint involvement was the commonest presenting manifestation (60%), followed by nephrotic syndrome (25%). Notable clinical features included a high incidence of renal involvement (75%), significant hypertension (45%) and reversibility of acute renal failure (2 cases). The other organs and systems involved included: mucocutaneous manifestations (60%), cardiovascular system (30%), respiratory system (25%), neuropsychiatric manifestations (45%), and anemia (75%). Raynaud's phenomenon and thrombocytopenia were rare while leucopenia was not seen in a single patient. Immunological abnormalities noted were 100% positivity for antinuclear antibodies, and 87.5 and 75% positivity for antibodies to double-stranded and single-stranded DNA, respectively. Hypocomplementemia was seen in 75% of patients tested.
在14年的时间里,共诊治了20例青春期前儿童(年龄小于14岁)的系统性红斑狼疮(SLE)。男女比例为1:2.3,平均发病年龄为9.37岁。发热伴关节受累是最常见的临床表现(60%),其次是肾病综合征(25%)。显著的临床特征包括肾脏受累发生率高(75%)、重度高血压(45%)以及急性肾衰竭的可逆性(2例)。其他受累的器官和系统包括:皮肤黏膜表现(60%)、心血管系统(30%)、呼吸系统(25%)、神经精神表现(45%)以及贫血(75%)。雷诺现象和血小板减少症罕见,无一例患者出现白细胞减少。检测到的免疫异常包括抗核抗体100%阳性,双链和单链DNA抗体分别为87.5%和75%阳性。75%接受检测的患者出现补体低下。