小肠免疫增殖性疾病继发的营养缺乏性多发性神经病
[Deficiency polyneuropathy secondary to immunoproliferative disease of the small intestine].
作者信息
Sopeña F, López Zaborras J, Nerin J M, Soria J, Sousa F L, Freile E
机构信息
Servicio de Aparato Digestivo, Hospital Clínico Universitario de Zaragoza.
出版信息
Rev Esp Enferm Dig. 1992 Dec;82(6):423-6.
PMID:1493062
Abstract
We report a new case of immunoproliferative small intestinal disease with neurological involvement expressed as deficiency polyneuropathy. In spite of non identifiable plasmatic paraprotein, the use of immunohistochemical techniques showed the characteristic proliferation in the intestinal mucosa of plasma cells with a prevalence of IgA cells, which define this disease.
摘要
我们报告了一例新的免疫增殖性小肠疾病病例，该病例伴有以多发性神经病变为表现的神经受累。尽管未检测到血浆副蛋白，但免疫组化技术显示，小肠黏膜中浆细胞呈特征性增殖，其中以IgA细胞为主，这是该疾病的特征。
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