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儿童期起病的系统性红斑狼疮的初始表现:一项法国多中心研究。

Initial presentation of childhood-onset systemic lupus erythematosus: a French multicenter study.

作者信息

Bader-Meunier B, Armengaud J B, Haddad E, Salomon R, Deschênes G, Koné-Paut I, Leblanc T, Loirat C, Niaudet P, Piette J C, Prieur A M, Quartier P, Bouissou F, Foulard M, Leverger G, Lemelle I, Pilet P, Rodière M, Sirvent N, Cochat P

机构信息

Department of Pediatrics, Hôpital de Bicêtre, 78 rue du Général Leclerc, 94276 Le Kremlin Bicêtre, France.

出版信息

J Pediatr. 2005 May;146(5):648-53. doi: 10.1016/j.jpeds.2004.12.045.

Abstract

OBJECTIVE

To describe the clinical and laboratory manifestations of childhood-onset systemic lupus erythematosus (SLE) at presentation.

STUDY DESIGN

This retrospective French multicenter study involved 155 patients in whom SLE developed before the age of 16 years. Mean patient age at onset was 11.5 +/- 2.5 years (range, 1.5-16 years). The female to male ratio was 4.5.

RESULTS

The most common initial manifestations were hematologic (72%), cutaneous (70%), musculoskeletal (64%), renal (50%), and fever (58%). Thirty-two percent of children had atypical symptoms, mainly including abdominal involvement in 26 patients, which lead to negative laparotomy results for presumed appendicitis. Severe renal, neurologic, hematologic, abdominal, cardiac, pulmonary, thrombotic, and/or cutaneous manifestations occurred within the first month after the diagnosis in 40% of patients. The mean erythrocyte sedimentation rate was 72 +/- 29 mm/h, and the mean C-reactive protein value 22 +/- 21 mg/L. Antinuclear antibodies an, anti-double stranded DNA antibodies, and low C3 or C4 level were retrieved in 97%, 93%, and 78 % of patients, respectively.

CONCLUSION

Initial manifestations of childhood-onset SLE are diverse and often severe. The diagnosis of SLE should be promptly considered in any febrile adolescent with unexplained organ involvement, especially when associated with an increased erythrocyte sedimentation rate.

摘要

目的

描述儿童期起病的系统性红斑狼疮(SLE)初发时的临床和实验室表现。

研究设计

这项回顾性法国多中心研究纳入了155例16岁之前发病的SLE患者。发病时患者的平均年龄为11.5±2.5岁(范围1.5 - 16岁)。男女比例为4.5。

结果

最常见的初始表现为血液系统(72%)、皮肤(70%)、肌肉骨骼(64%)、肾脏(50%)及发热(58%)。32%的儿童有非典型症状,主要包括26例腹部受累,这导致因疑似阑尾炎而行剖腹探查结果为阴性。40%的患者在诊断后的第一个月内出现严重的肾脏、神经、血液、腹部、心脏、肺部、血栓形成及/或皮肤表现。平均红细胞沉降率为72±29mm/h,平均C反应蛋白值为22±21mg/L。分别在97%、93%和78%的患者中检测到抗核抗体、抗双链DNA抗体以及低C3或C4水平。

结论

儿童期起病的SLE初始表现多样且常较严重。对于任何有不明原因器官受累的发热青少年,尤其是伴有红细胞沉降率升高时,应及时考虑SLE的诊断。

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