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患者患有反应性淋巴组织增生伴 IgG4 阳性细胞增多,出现多发性单神经炎和肿块样细胞浸润。

Mononeuritis multiplex with tumefactive cellular infiltration in a patient with reactive lymphoid hyperplasia with increased immunoglobulin G4-positive cells.

机构信息

Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya466-8550, Japan.

Department of Pathology, Nagoya University Graduate School of Medicine, Nagoya466-8550, Japan.

出版信息

Hum Pathol. 2014 Feb;45(2):427-30. doi: 10.1016/j.humpath.2013.07.047. Epub 2013 Nov 27.

DOI:10.1016/j.humpath.2013.07.047
PMID:24289971
Abstract

We describe a 54-year-old man with mononeuritis multiplex and reactive lymphoid hyperplasia with increased immunoglobulin G4 (IgG4)-positive cells. Asymmetrical numbness and weakness had advanced stepwise for 6 years. Serum immunoglobulin G, IgG4, and immunoglobulin E levels were elevated, whereas M protein was not detected. Chest and abdominal computed tomography showed generalized lymphadenopathy. Inguinal lymph node biopsy revealed expansion of the interfollicular area with infiltration of IgG4-positive cells, of which the absolute number was greater than 100 per high-power field, and the percentage of IgG4+/immunoglobulin G+ plasma cells was 33%. Sural nerve biopsy disclosed axonal neuropathy with tumefactive lymphoid infiltrate in epineurium, but IgG4-positve plasma cells and fibrosis were not detected. Symptoms and laboratory data were improved with oral glucocorticoid therapy at a dose of 0.6 mg/kg per day. Although the causal mechanisms of neuropathy should be determined in future studies, peripheral nerve involvement may occur in patients with reactive lymphoid hyperplasia with increased IgG4-positive cells.

摘要

我们描述了一位 54 岁男性,患有多发性单神经炎和反应性淋巴组织增生伴 IgG4 阳性细胞增多。非对称性麻木和无力进行性加重 6 年。血清免疫球蛋白 G、IgG4 和免疫球蛋白 E 水平升高,但未检测到 M 蛋白。胸部和腹部计算机断层扫描显示全身淋巴结病。腹股沟淋巴结活检显示滤泡间区扩张,伴有 IgG4 阳性细胞浸润,其中高倍视野下绝对数量大于 100,IgG4+/免疫球蛋白 G+浆细胞的百分比为 33%。腓肠神经活检显示轴索神经病伴神经外膜瘤样淋巴浸润,但未检测到 IgG4 阳性浆细胞和纤维化。口服糖皮质激素治疗(每天 0.6mg/kg)后症状和实验室数据改善。尽管在未来的研究中应确定神经病的因果机制,但在伴有 IgG4 阳性细胞增多的反应性淋巴组织增生患者中可能会发生周围神经受累。

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