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[施尼茨勒综合征作为不明原因反复发热的一个病因]

[The Schnitzler syndrome as a cause of recurrent fever of unknown origin].

作者信息

Winckelmann G, Nagel H G, Maier R, Reuther G

机构信息

Deutsche Klinik für Diagnostik, Wiesbaden.

出版信息

Dtsch Med Wochenschr. 1996 Jul 5;121(27):860-4. doi: 10.1055/s-2008-1043079.

Abstract

HISTORY AND CLINICAL FINDINGS

For 4 years a 56-year-old woman had been suffering from chronic urticaria. In the past two years she had developed recurrent fever, each 1-3 days in duration. In the last 6 to 8 months she also had severe aching in the legs. There were no significant findings on physical examination other than non-itching urticarial rash over trunk and limbs.

INVESTIGATIONS

Blood sedimentation rate was increased (maximum 88/110 mm), as were WBC count (16,200/microliter, 83% neutrophils) and the activity of alkaline leucocyte phosphatase (225 U/l). Monoclonal IgM gammopathy type kappa and circulating IgM immune complex (15.4 mg/dl) were demonstrated in serum. Skin biopsy of a new urticarial lesion revealed vasculitis. Iliac crest biopsy was unremarkable and showed no lymphoid cell infiltration. Bone scintigraphy revealed bilaterally increased storage in femur and tibia. Magnetic resonance imaging demonstrated marrow infiltration without space-occupying features in the affected femur and tibia.

TREATMENT AND COURSE

Conjunction of fever, generalised urticaria, joint/bone pain and monoclonal gammopathy of kappa type having established the diagnosis of Schnitzler's syndrome, treatment with ibuprofen was started (initially 1,200 mg daily by mouth, followed by reduction to 600 mg daily). All symptoms rapidly improved and the bone changes regressed, but not the monoclonal gammopathy. But when the ibuprofen dosage had been decreased to 600 mg daily, the urticaria recurred, though in milder form.

CONCLUSION

This case demonstrates the efficacy of ibuprofen in the treatment of the Schnitzler's syndrome. Furthermore reversibility of scintigraphic bone lesions could be demonstrated under ibuprofen treatment.

摘要

病史及临床检查结果

一名56岁女性患慢性荨麻疹4年。在过去两年中,她反复发热,每次持续1 - 3天。在过去6至8个月里,她还出现了严重的腿部疼痛。体格检查除躯干和四肢有非瘙痒性荨麻疹皮疹外,无其他明显异常。

检查

血沉加快(最高88/110mm),白细胞计数(16,200/微升,83%为中性粒细胞)及碱性白细胞磷酸酶活性(225U/l)均升高。血清中检测到κ型单克隆IgM丙种球蛋白病及循环IgM免疫复合物(15.4mg/dl)。新出现的荨麻疹皮损皮肤活检显示血管炎。髂嵴活检无异常,未发现淋巴细胞浸润。骨闪烁显像显示双侧股骨和胫骨放射性摄取增加。磁共振成像显示受累股骨和胫骨有骨髓浸润,但无占位性病变。

治疗及病程

发热、全身性荨麻疹、关节/骨痛及κ型单克隆丙种球蛋白病同时存在,确诊为施尼茨勒综合征,开始用布洛芬治疗(最初口服每日1200mg,随后减至每日600mg)。所有症状迅速改善,骨改变消退,但单克隆丙种球蛋白病未改善。但当布洛芬剂量减至每日600mg时,荨麻疹复发,不过症状较轻。

结论

本病例证明布洛芬对施尼茨勒综合征治疗有效。此外,在布洛芬治疗下,骨闪烁显像病变可显示具有可逆性。

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