Murray C S, Cohen A, Perkins T, Davidson J E, Sills J A
Department of Paediatric Rheumatology, Royal Liverpool Childrens Hospital, Eaton Road, Liverpool L12 2AP, UK.
Arch Dis Child. 2000 Mar;82(3):231-3. doi: 10.1136/adc.82.3.231.
Reflex sympathetic dystrophy (RSD), an unusual diagnosis in general paediatrics, is well recognised by paediatric rheumatologists. This study reports the presentation and the clinical course of 46 patients (35 female, age range 8-15.2) with RSD. The patients saw professionals from an average of 2.3 specialties (range 1-5). Twenty five (54%) had a history of trauma. Median time to diagnosis was 12 weeks (range 1-130). Many children had multiple investigations and treatments. Once diagnosis was made, treatment followed with physiotherapy and analgesics. Median time to recovery was seven weeks (range 1-140), with 27.5% relapsing. Nine children required assessment by the child and adolescent psychiatry team. This disease, though rare, has significant morbidity and it is therefore important to raise clinicians' awareness of RSD in childhood. Children with the condition may then be recognised and referred for appropriate management earlier, and spared unnecessary investigations and treatments which may exacerbate the condition.
反射性交感神经营养不良(RSD)在普通儿科中是一种不常见的诊断,但儿科风湿病学家对此有充分认识。本研究报告了46例RSD患者(35例女性,年龄范围8至15.2岁)的临床表现和临床病程。患者平均看过2.3个专科的专业医生(范围为1至5个)。25例(54%)有创伤史。诊断的中位时间为12周(范围1至130周)。许多儿童接受了多项检查和治疗。一旦确诊,便采用物理治疗和止痛药物进行治疗。恢复的中位时间为7周(范围1至140周),27.5%的患者复发。9名儿童需要儿童和青少年精神科团队进行评估。这种疾病虽然罕见,但发病率很高,因此提高临床医生对儿童RSD的认识很重要。这样,患有该疾病的儿童可能会更早被识别并转诊接受适当治疗,避免不必要的检查和治疗,因为这些可能会加重病情。