Reflex sympathetic dystrophy: complex regional pain syndrome type I in children with mitochondrial disease and maternal inheritance

被引:27
作者
Higashimoto, T. [1 ,2 ,3 ,4 ]
Baldwin, E. E. [1 ,2 ,5 ]
Gold, J. I. [3 ,6 ,7 ]
Boles, R. G. [1 ,2 ,3 ]
机构
[1] Childrens Hosp Los Angeles, Div Med Genet, Los Angeles, CA 90027 USA
[2] Childrens Hosp Los Angeles, Saban Res Inst, Los Angeles, CA 90027 USA
[3] Univ So Calif, Dept Pediat, Keck Sch Med, Los Angeles, CA 90089 USA
[4] Childrens Hosp, Med Ctr, Div Expt Hematol, Cincinnati, OH 45229 USA
[5] Univ So Calif, Dept Psychiatry & Behav Sci, Los Angeles, CA USA
[6] Univ So Calif, Dept Anesthesiol, Keck Sch Med, Los Angeles, CA USA
[7] Childrens Hosp Los Angeles, Dept Anesthesiol Crit Care Med Comfort Pain Manag, Los Angeles, CA 90027 USA
关键词
D O I
10.1136/adc.2007.123661
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective: Complex regional pain syndrome type I (CRPS-I), previously known as reflex sympathetic dystrophy (RSD), is an idiopathic condition characterised by localised, abnormally intense and prolonged pain, allodynia and autonomic nervous system changes (ie, swelling, skin colour and temperature changes and altered perspiration) that usually appear following a "noxious'' trigger such as trauma or surgery. The objective of this report is to demonstrate that children with CRPS-I can have additional dysautonomic conditions secondary to an underlying maternally inherited mitochondrial disease, an association not previously published. Methods: Medical records of about 500 patients seen by one paediatric metabolic geneticist were reviewed to identify children meeting established CRPS diagnostic criteria. Results: CRPS-I was present in eight children in seven families, each of which also had additional functional/dysautonomic conditions, the most common (>= 4 cases per condition) being gastrointestinal dysmotility, migraine, cyclic vomiting and chronic fatigue. All seven probands studied met Nijmegen ( 2002) diagnostic criteria for definite mitochondrial disease on the basis of the clinical signs and symptoms and biochemical analyses. Six of the seven families met our pedigree-based criteria for probable maternal inheritance. Conclusion: In one tertiary-care paediatric genetics practice, children meeting the CRPS-I diagnostic criteria frequently had additional autonomic-related conditions secondary to maternally inherited mitochondrial disease, suggesting that mitochondrial DNA sequence variants can predispose children towards the development of CRPS-I and other dysautonomias. CRPS-I should be considered in patients with mitochondrial disease who complain of idiopathic pain. Maternally inherited mitochondrial disease may not be a rare cause of CRPS-I, especially in children who present with other manifestations of dysautonomia.
引用
收藏
页码:390 / 397
页数:8
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