【trap综合征,一种罕见原因不明的发热:病例报告及文献回顾】。

Maurizio Benucci, Gabriele Nenci, Gianni Taccetti, Aurelio Rosso, Carlo Cappelletti
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引用次数: 0

摘要

肿瘤坏死因子(TNF)受体相关周期性综合征(TRAPS)是一种常染色体显性遗传病,表现为周期性发热和疼痛。TRAPS是由位于12p13的TNFRSF1A基因突变引起的。该基因编码p55 tnf - α受体的细胞外区域,导致受体的膜表达形式的切割受损和下调,受体潜在拮抗可溶性形式的脱落减少,结果是tnf - α作用不平衡。大多数受影响的患者来自北欧。发热、无菌性腹膜炎、胸膜痛、关节痛、肌痛、皮疹和/或结膜炎发生在综合征发作期间;有些患者还会发生全身性淀粉样变,患者之间存在一些差异。急性期反应发生在发作期间。我们描述一个23岁的摩尔达维亚妇女,住在意大利表现反复发烧发作腹痛和皮疹。活检显示小血管炎。遗传分析显示TNFRSF1A基因(R92Q)突变。本文也对这一罕见疾病的文献作一综述。
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[TRAPS syndrome, a rare cause of fever of unknown origin: case report and review of the literature].

Tumor necrosis factor (TNF) receptor-associated periodic syndrome (TRAPS) is an autosomal dominant inherited condition of periodic fever and pain. TRAPS is caused by mutations of the TNFRSF1A gene localized at 12p13. The gene encodes extracellular region of the p55 TNF-alpha receptor, resulting in impaired cleavage and down-regulation of the membrane expressed form of the receptor, a diminished shedding of potentially antagonistic soluble form of the receptor and, as a consequence, an unbalanced TNF-alpha action. Most affected patients are from northern Europe. Fever, sterile peritonitis, pleural pain, arthralgia, myalgia, skin rash, and/or conjunctivitis occur during the syndrome episodes; some patients also develop systemic amyloidosis, with some differences among patients. An acute-phase response occurs during the episodes. We describe a case of a 23-year-old Moldavian woman, living in Italy presenting recurrent fever episodes with abdominal pain and skin rash. A biopsy showed small vessel vasculitis. The genetic analysis showed a TNFRSF1A gene (R92Q) mutation. In this paper we report also a literature review on this rare disease.

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