Bejia Ismail, Ben Khalifa Anis, Ben Salah Zohra, Bejaoui Samia, Touzi Mongi, Bergaoui Naceur
Servide de Rhumatologie, EPS Monastir.
Tunis Med. 2005 Mar;83(3):163-7.
We analysed 60 cases of algodystrophy admitted in the rheumatology department of the university hospital of Monastir. We used a univariate analysis to search the factors associated with the disease evolution. Our patients were 40 males and 20 females. The mean age was 51.6 ans (16 - 81). The traumatisme was the dominant cause (46.7% of the cases). Calcitonines were used in 70% of the cases. Functional results at one year were satisfying and not satisfying in 62.5% and 37.5% of the cases, respectively. The primitive algodystrophy was associated with a satisfying result. Sequella were observed in 10.5% of the cases. The primitive algodystrophy was associated with a satisfying result. Algodystrophy remain a benign disease and the best treatment remains the preventive one mainly in traumatic and orthopaedic circumstances.
我们分析了在莫纳斯提尔大学医院风湿病科收治的60例反射性交感神经营养不良病例。我们采用单因素分析来寻找与疾病进展相关的因素。我们的患者中有40名男性和20名女性。平均年龄为51.6岁(16 - 81岁)。创伤是主要病因(占病例的46.7%)。70%的病例使用了降钙素。一年时的功能结果在62.5%的病例中令人满意,在37.5%的病例中不满意。原发性反射性交感神经营养不良与满意的结果相关。10.5%的病例观察到后遗症。原发性反射性交感神经营养不良与满意的结果相关。反射性交感神经营养不良仍然是一种良性疾病,最佳治疗仍然主要是在创伤和骨科情况下的预防性治疗。