Clinical features of the course of polyarteritis nodosa in combination with familial Mediterranean fever

L. P. Petrosyan, M. Sargsyan, V. O. Petrosyan, V. N. Mukuchyan
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Abstract

There are certain difficulties with diagnosing of poliarteritis nodoza, that is explained by the folllowung factors: non-specificity of the initial symptoms, polymorphism of clinical manifestations, the abcence of specific laboratory markers. Тhe diagnosis is made primarily on the basis of the clinical picture, that becomes apparent during the first three months of illness. The abcence of a detailed clinical picture does not exclude the presense of poliarteritis nodoza. It may be explained by the concomitant pathology, in this case periodic illness (familian mediterranean fever). Due to medical literature data, poliarteritis nodoza is surely associated with periodic illness. The prevalence of poliarteritis nodoza in general population is about 6 on 100 000 people.The prevalence of poliarteritis nodoza among the patients suffering from periodic illness is 1%. The patients when they are diagnosed polyarteritis nodosa in association with periodic illness are younger than the patients when they are diagnosed only polyarteritis nodosa. It turned out to be interesting that the treatment of patients with polyarteritis nodosa in association with periodic illness through glucocorticoid drugs in the combination with colchicines proved to be successful and resulted in remission.
结节性多动脉炎合并家族性地中海热病程的临床特征
结节性脊髓灰质炎的诊断存在一定困难,原因如下:初期症状无特异性、临床表现多态性、缺乏特异性实验室指标。诊断主要依据病程头三个月的临床表现。没有详细的临床表现并不排除患有结节性脊髓灰质炎。在这种情况下,周期性疾病(家族性地中海热)也可以解释为结节性多发性动脉炎。根据医学文献资料,结节性多发性大动脉炎肯定与周期性疾病有关。结节性多发性大动脉炎在普通人群中的发病率约为十万分之六。被诊断为结节性多动脉炎并伴有周期性疾病的患者比仅被诊断为结节性多动脉炎的患者更年轻。有趣的是,通过糖皮质激素药物与秋水仙碱联合治疗结节性多动脉炎合并周期性疾病的患者被证明是成功的,并导致病情缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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