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一名患有副肿瘤性视网膜病变加小纤维多发性神经病并与华氏巨球蛋白血症(淋巴浆细胞淋巴瘤)相关的男性:对发病机制的见解

A Man with Paraneoplastic Retinopathy plus Small Fiber Polyneuropathy Associated with Waldenström Macroglobulinemia (Lymphoplasmacytic Lymphoma): Insights into Mechanisms.

作者信息

Liu Yingna, Magro Cynthia, Loewenstein John I, Makar Robert S, Stowell Christopher P, Dzik Walter H, Hochberg Ephraim P, Oaklander Anne Louise, Sobrin Lucia

机构信息

a Department of Ophthalmology , Massachusetts Eye and Ear Infirmary, Harvard Medical School , Boston , Massachusetts , USA .

b Department of Pathology and Laboratory Medicine , Weill Cornell Medical College of Cornell University , New York , USA .

出版信息

Ocul Immunol Inflamm. 2015;23(5):405-9. doi: 10.3109/09273948.2014.884599. Epub 2014 Mar 21.

Abstract

PURPOSE

To report a well-characterized Waldenström's macroglobulinemia (WM) case that provides insight into the mechanisms of two paraneoplastic complications -- cancer-associated retinopathy (CAR) and small fiber polyneuropathy (SFPN).

METHODS

Retrospective medical chart review.

RESULTS

A 58-year old man with WM developed vision loss and bilateral lower extremity pain. CAR was diagnosed by history, a depressed electroretinogram (ERG) and positive anti-retinal antibodies. SFPN diagnosis was based on abnormal autonomic nerve function testing and a distal-leg skin biopsy that demonstrated absent epidermal small-fiber innervation, IgM and complement deposition and microvasculopathy. Plasma exchange (PLEX) led to dramatic pain relief and subjective improvement in eye symptoms along with improvement of some ERG parameters. Repeat skin biopsy after treatment showed less microvascular abnormalities and decreased complement deposition.

CONCLUSIONS

The concurrence of CAR and SFPN in this patient suggest that both were complications of WM and their common response to PLEX suggests co-mediation by humoral factors that accessed target antigens through IgM-triggered, complement-mediated vascular damage.

摘要

目的

报告一例特征明确的华氏巨球蛋白血症(WM)病例,该病例有助于深入了解两种副肿瘤并发症——癌症相关性视网膜病变(CAR)和小纤维多发性神经病(SFPN)的发病机制。

方法

回顾性查阅病历。

结果

一名58岁的WM男性患者出现视力丧失和双侧下肢疼痛。根据病史、视网膜电图(ERG)降低及抗视网膜抗体阳性诊断为CAR。SFPN的诊断基于自主神经功能测试异常以及远端腿部皮肤活检,活检显示表皮小纤维神经支配缺失、IgM和补体沉积以及微血管病变。血浆置换(PLEX)使疼痛显著缓解,眼部症状主观改善,同时一些ERG参数也有所改善。治疗后重复皮肤活检显示微血管异常减少,补体沉积减少。

结论

该患者同时出现CAR和SFPN,提示两者均为WM的并发症,它们对PLEX的共同反应表明是由体液因子共同介导的,这些体液因子通过IgM触发、补体介导的血管损伤作用于靶抗原。

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