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本文引用的文献

1
Two familial cases with tumor necrosis factor receptor-associated periodic syndrome caused by a non-cysteine mutation (T50M) in the TNFRSF1A gene associated with severe multiorganic amyloidosis.两例家族性病例,由TNFRSF1A基因中的非半胱氨酸突变(T50M)导致肿瘤坏死因子受体相关周期性综合征,并伴有严重的多器官淀粉样变性。
J Rheumatol. 2004 Dec;31(12):2519-22.
2
Small vessel vasculitis and relapsing panniculitis in tumour necrosis factor receptor associated periodic syndrome (TRAPS).肿瘤坏死因子受体相关周期性综合征(TRAPS)中的小血管血管炎和复发性脂膜炎。
Ann Rheum Dis. 2004 Nov;63(11):1518-20. doi: 10.1136/ard.2003.016733.
3
Shedding of mutant tumor necrosis factor receptor superfamily 1A associated with tumor necrosis factor receptor-associated periodic syndrome: differences between cell types.与肿瘤坏死因子受体相关的周期性综合征相关的突变型肿瘤坏死因子受体超家族1A的脱落:细胞类型之间的差异
Arthritis Rheum. 2004 Aug;50(8):2651-9. doi: 10.1002/art.20380.
4
Infevers: an evolving mutation database for auto-inflammatory syndromes.Infevers:一个不断发展的自身炎症性综合征突变数据库。
Hum Mutat. 2004 Sep;24(3):194-8. doi: 10.1002/humu.20080.
5
TNFRSF1A-associated periodic syndrome (TRAPS), Muckle-Wells syndrome (MWS) and renal amyloidosis.肿瘤坏死因子受体超家族成员1A相关周期性综合征(TRAPS)、穆克-韦尔斯综合征(MWS)和肾淀粉样变性。
J Nephrol. 2003 May-Jun;16(3):435-7.
6
Prospective study of anti-tumour necrosis factor receptor superfamily 1B fusion protein, and case study of anti-tumour necrosis factor receptor superfamily 1A fusion protein, in tumour necrosis factor receptor associated periodic syndrome (TRAPS): clinical and laboratory findings in a series of seven patients.肿瘤坏死因子受体超家族1B融合蛋白在肿瘤坏死因子受体相关周期性综合征(TRAPS)中的前瞻性研究及肿瘤坏死因子受体超家族1A融合蛋白的病例研究:7例患者的临床和实验室检查结果
Rheumatology (Oxford). 2003 Feb;42(2):235-9. doi: 10.1093/rheumatology/keg070.
7
The expanding spectrum of systemic autoinflammatory disorders and their rheumatic manifestations.系统性自身炎症性疾病及其风湿性表现的不断扩大的范围。
Curr Opin Rheumatol. 2003 Jan;15(1):61-9. doi: 10.1097/00002281-200301000-00011.
8
The TNF receptor-associated periodic syndrome (TRAPS): emerging concepts of an autoinflammatory disorder.肿瘤坏死因子受体相关周期性综合征(TRAPS):自身炎症性疾病的新观念
Medicine (Baltimore). 2002 Sep;81(5):349-68. doi: 10.1097/00005792-200209000-00002.
9
The enlarging clinical, genetic, and population spectrum of tumor necrosis factor receptor-associated periodic syndrome.肿瘤坏死因子受体相关周期性综合征不断扩大的临床、遗传及人群范围。
Arthritis Rheum. 2002 Aug;46(8):2181-8. doi: 10.1002/art.10429.
10
Mutational spectrum in the MEFV and TNFRSF1A genes in patients suffering from AA amyloidosis and recurrent inflammatory attacks.患有AA型淀粉样变性和复发性炎症发作患者的MEFV和TNFRSF1A基因的突变谱。
Nephrol Dial Transplant. 2002 Jul;17(7):1212-7. doi: 10.1093/ndt/17.7.1212.

无发热的“周期性发热”:两例肿瘤坏死因子受体超家族成员1A基因(TNFRSF1A)突变的无发热型肿瘤坏死因子受体相关周期性综合征,表现为炎症发作或单症状性淀粉样变性。

"Periodic fever" without fever: two cases of non-febrile TRAPS with mutations in the TNFRSF1A gene presenting with episodes of inflammation or monosymptomatic amyloidosis.

作者信息

Kallinich T, Haffner D, Rudolph B, Schindler R, Canaan-Kühl S, Keitzer R, Burmester G R, Roesen-Wolff A, Roesler J

机构信息

Department of Paediatric Pulmonology and Immunology, Charité Campus Virchow-Klinikum, Universitaetsmedizin Berlin, Germany.

出版信息

Ann Rheum Dis. 2006 Jul;65(7):958-60. doi: 10.1136/ard.2005.043570. Epub 2005 Nov 24.

DOI:10.1136/ard.2005.043570
PMID:16308343
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1798226/
Abstract

BACKGROUND

Tumour necrosis factor (TNF) receptor associated periodic syndrome (TRAPS) is caused by dominant mutations in the TNFRSF1A gene. In typical cases TRAPS begins early in childhood and is characterised by high and remittent fever over a period of 1-4 weeks or longer, accompanied by systemic and local inflammation.

CASE REPORTS

Patient 1 presented with recurrent episodes of weakness, migrating myalgias, arthralgias, exanthema, and chest pain lasting for 1-4 weeks, but without any fever over an initial period of 4 years at least. Diagnosis of TRAPS was confirmed by the heterozygous mutation Y20H in TNFRSF1A. Patient 2, a 23 year old woman never had any symptoms indicative of TRAPS. Genetic evaluation of all members of her family with a TRAPS index patient disclosed the T50M mutation in TNFRSF1A. A medical check up showed proteinuria, and renal biopsy disclosed AA amyloidosis.

CONCLUSIONS

TRAPS associated mutations can induce considerable inflammation that is not necessarily accompanied by fever. Even monosymptomatic severe amyloidosis can occur in these patients. Genetic counselling and appropriate management to prevent or mitigate amyloidosis may be necessary.

摘要

背景

肿瘤坏死因子(TNF)受体相关周期性综合征(TRAPS)由TNFRSF1A基因的显性突变引起。典型病例中,TRAPS起病于儿童早期,特征为持续1 - 4周或更长时间的高热和弛张热,伴有全身和局部炎症。

病例报告

患者1表现为反复发作的乏力、游走性肌痛、关节痛、皮疹和胸痛,持续1 - 4周,但在至少最初4年期间无发热。通过TNFRSF1A基因杂合突变Y20H确诊为TRAPS。患者2,一名23岁女性,从未有任何提示TRAPS的症状。对其家族中一名TRAPS索引患者的所有家庭成员进行基因评估,发现TNFRSF1A基因存在T50M突变。医学检查显示蛋白尿,肾活检显示AA型淀粉样变性。

结论

TRAPS相关突变可引发相当程度的炎症,不一定伴有发热。这些患者甚至可能出现单症状性严重淀粉样变性。可能需要进行遗传咨询和适当管理以预防或减轻淀粉样变性。