Manki Akira, Nishikomori Ryuta, Nakata-Hizume Mami, Kunitomi Taiji, Takei Syuji, Urakami Tomoko, Morishima Tsuneo
Department of Pediatrics, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Allergol Int. 2006 Sep;55(3):337-41. doi: 10.2332/allergolint.55.337.
We report two cases of tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in patients in whom systemic juvenile idiopathic arthritis (JIA) had initially been diagnosed or suspected. One patient, given a diagnosis of systemic JIA, was a 10-year-old boy who had presented with recurrent episodes of spike-fever, skin rash, arthritis, and myalgia. The other patient was his 7-year-old sister, who presented with similar symptoms and was suspected of having systemic JIA.
Serum levels of soluble tumor necrosis factor receptor super family 1A (TNFRSF1A), TNF-alpha, Interleukin (IL) -6, and C-reactive protein (CRP) were measured in two siblings and JIA patients. In addition, DNA sequencing of the TNFRSF1A gene in two siblings was also performed.
A detailed family history showed that their mother had an episode of recurrent fever, arthritis, and myalgia with an increased serum CRP after the delivery of a daughter. Both siblings had serum levels of soluble TNFRSF1A that were below the normal reference range, and that did not reach a level corresponding to that of systemic JIA. On TNFRSF1A gene analysis, a single missense mutation resulting in C30Y was found in both siblings.
Based on the clinical features and the TNFRSF1A mutation, both siblings were given a diagnosis of TRAPS. The serum levels of soluble TNFRSF1A, measured along with the CRP level, may be a useful screening marker for differentiating TRAPS from systemic JIA.
我们报告了两例最初被诊断或怀疑为全身型幼年特发性关节炎(JIA)的患者,最终确诊为肿瘤坏死因子受体相关周期性综合征(TRAPS)。其中一名患者为10岁男孩,最初被诊断为全身型JIA,表现为反复高热、皮疹、关节炎和肌痛。另一名患者是他7岁的妹妹,出现了类似症状,最初被怀疑患有全身型JIA。
检测了这两名同胞以及JIA患者血清中可溶性肿瘤坏死因子受体超家族1A(TNFRSF1A)、肿瘤坏死因子-α(TNF-α)、白细胞介素(IL)-6和C反应蛋白(CRP)的水平。此外,还对这两名同胞的TNFRSF1A基因进行了DNA测序。
详细的家族史显示,他们的母亲在生下女儿后曾出现反复发热、关节炎和肌痛,血清CRP升高。两名同胞的可溶性TNFRSF1A血清水平均低于正常参考范围,且未达到全身型JIA相应水平。在TNFRSF1A基因分析中,两名同胞均发现了导致C30Y的单一错义突变。
根据临床特征和TNFRSF1A突变,两名同胞均被诊断为TRAPS。结合CRP水平检测的可溶性TNFRSF1A血清水平,可能是区分TRAPS与全身型JIA的有用筛查标志物。