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硬化性黏液水肿:对大剂量静脉注射免疫球蛋白(hdIVIg)的反应

Scleromyxedema: response to high-dose intravenous immunoglobulin (hdIVIg).

作者信息

Lister R K, Jolles S, Whittaker S, Black C, Forgacs I, Cramp M, Potter M, Rustin M H

机构信息

Department of Dermatology, Royal Free Hospital, London, UK.

出版信息

J Am Acad Dermatol. 2000 Aug;43(2 Pt 2):403-8. doi: 10.1067/mjd.2000.104001.

DOI:10.1067/mjd.2000.104001
PMID:10901735
Abstract

We report 2 patients with scleromyxedema, both associated with IgG-lambda paraproteinemia, who were treated with high-dose intravenous immunoglobulin (hdIVIg) 2g/kg per month. The response to treatment was assessed using an objective skin scoring system initially established for patients with scleroderma. This system grades the overall severity of the induration and the reduction in mobility of the skin. Both patients initially had a dramatic response to treatment which was sustained in one patient. The first patient, a 30-year-old black man, showed a reduction in skin scores from 36/60 to 11/60 over a 3-month period, during which time he had 3 infusions of hdIVIg. After an unplanned 2-month break from treatment, severe neuromuscular complications developed. These improved initially with more frequent infusions of hdIVIg but oral corticosteroids were required to treat worsening myopathy. Unfortunately, the initial response to hdIVIg has not been sustained and his skin scores at 1 year returned to baseline. The second patient, a 60-year-old white man, showed a similarly dramatic reduction in skin scores from 36/60 to 15/60 over a 3-month period after having received only 2 infusions of hdIVIg. There has been sustained improvement after 10 months of therapy and the interval between hdIVIg infusions has been increased to 10 weeks without deterioration. HdIVIg may be an effective treatment for some patients with scleromyxedema, a rare condition with few effective treatments and a poor prognosis.

摘要

我们报告了2例硬肿病患者,均伴有IgG-λ副蛋白血症,每月接受2g/kg的大剂量静脉注射免疫球蛋白(hdIVIg)治疗。使用最初为硬皮病患者建立的客观皮肤评分系统评估治疗反应。该系统对硬结的总体严重程度和皮肤活动度降低进行分级。两名患者最初对治疗均有显著反应,其中一名患者反应持续。第一名患者是一名30岁的黑人男性,在3个月内皮肤评分从36/60降至11/60,在此期间他接受了3次hdIVIg输注。在无计划中断治疗2个月后,出现了严重的神经肌肉并发症。这些并发症最初通过更频繁的hdIVIg输注有所改善,但需要口服皮质类固醇来治疗不断恶化的肌病。不幸的是,对hdIVIg的初始反应未能持续,他1年后的皮肤评分恢复到基线水平。第二名患者是一名60岁的白人男性,在仅接受2次hdIVIg输注后的3个月内,皮肤评分同样从36/60显著降至15/60。经过10个月的治疗后病情持续改善,hdIVIg输注间隔已延长至10周且病情未恶化。对于一些硬肿病患者,hdIVIg可能是一种有效的治疗方法,硬肿病是一种罕见病,有效治疗方法很少且预后较差。

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