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儿童及青少年狼疮性肾炎

Lupus nephritis in childhood and adolescence.

作者信息

Cameron J S

机构信息

Renal Unit, Guy's Hospital, London, UK.

出版信息

Pediatr Nephrol. 1994 Apr;8(2):230-49. doi: 10.1007/BF00865490.

Abstract

Lupus nephritis in childhood usually presents after the age of 10 years, and presentation under 5 years is very rare. More males (F:M ratio 4.5:1) are affected than in adult-onset cases, but the ratio is the same in prepubertal and pubertal children. The incidence of clinically evident renal disease is greater at onset than in adults (82%), the usual presentation being with proteinuria, 50% having a nephrotic syndrome. Half the children show World Health Organisation class IV nephritis in renal biopsies. Neuropsychiatric lupus is present at onset in 30%, may complicate 50% at some point and remains a major problem. Prognosis has improved greatly over the past 30 years, at least in part the result of immunosuppressive treatment. Treatment of the initial phase may be guided by the severity of the renal biopsy appearances, more aggressive treatment including cytotoxic agents, i.v. methylprednisolone and perhaps plasma exchange, although the value of exchange is not established. Controversy persists as to the most effective cytotoxic treatment in the acute phase, both oral and i.v. cyclophosphamide and azathioprine being used in different units. In the chronic maintenance phase it seems established both clinically and histologically that addition of a cytotoxic agent improves outcome, but again the drug and route of administration are contentious. Azathioprine has the advantage of being safe for pregnancy and not gonadotoxic, whilst i.v. cyclophosphamide has been demonstrated to improve results over prednisolone alone in controlled trials and has advantages in non-compliant patients. No trial comparing the two regimes has been carried out, and one is needed. Today children much less commonly go into renal failure, and the main causes of actual death (15% of patients over 10 years) are now infections and extra-renal manifestations of lupus, principally neurological. Morbidity of the disease and the treatment remain a major problem, especially when treatment exacerbates complications of the disease itself, such as infections, osteonecrosis, thrombosis, vascular disease and possibly neoplasia.

摘要

儿童狼疮性肾炎通常在10岁以后发病,5岁以下发病极为罕见。与成人发病的病例相比,受影响的男性更多(女性与男性比例为4.5:1),但在青春期前和青春期儿童中该比例相同。临床明显的肾脏疾病在发病时的发生率高于成人(82%),通常表现为蛋白尿,50%的患儿患有肾病综合征。一半的儿童在肾活检中显示为世界卫生组织IV级肾炎。30%的患儿在发病时存在神经精神性狼疮,50%的患儿在病程中可能出现并发症,这仍然是一个主要问题。在过去30年中,预后有了很大改善,至少部分是免疫抑制治疗的结果。初始阶段的治疗可根据肾活检表现的严重程度来指导,更积极的治疗包括细胞毒性药物、静脉注射甲基泼尼松龙,可能还包括血浆置换,尽管血浆置换的价值尚未确定。关于急性期最有效的细胞毒性治疗仍存在争议,不同单位使用口服和静脉注射环磷酰胺以及硫唑嘌呤。在慢性维持阶段,临床和组织学上似乎都证实添加细胞毒性药物可改善预后,但药物和给药途径仍存在争议。硫唑嘌呤的优点是对妊娠安全且无性腺毒性,而在对照试验中已证明静脉注射环磷酰胺比单独使用泼尼松龙能改善结果,并且对不依从的患者有优势。尚未进行比较这两种治疗方案的试验,需要进行这样的试验。如今儿童肾衰竭的情况已不常见,实际死亡的主要原因(10岁以上患者的15%)现在是感染和狼疮的肾外表现,主要是神经方面的表现。该疾病及其治疗的发病率仍然是一个主要问题,特别是当治疗加重疾病本身的并发症时,如感染、骨坏死、血栓形成、血管疾病以及可能的肿瘤。

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