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阿尔及利亚人的免疫增殖性小肠疾病。II. α链病的超微结构研究。

Immunoproliferative small intestinal disease in Algerians. II. Ultrastructural studies in alpha-chain disease.

作者信息

Crow J, Asselah F

出版信息

Cancer. 1984 Nov 1;54(9):1908-13. doi: 10.1002/1097-0142(19841101)54:9<1908::aid-cncr2820540922>3.0.co;2-#.

Abstract

The plasma cell infiltrate of the small intestine in alpha-chain disease has been studied ultrastructurally in an attempt to determine whether there is a significant nuclear-cytoplasmic asynchrony that could be used as evidence for the neoplastic nature of the disease, even in its early stages. No such asynchrony was identified. In the early stages of the disease, the infiltrate was mainly of slightly immature plasma cells indistinguishable from those of coeliac disease. Later stages were marked by the presence of less differentiated immunoblastic cells arising in the deep mucosa and infiltrating into glands. Multinucleate plasmacytoid cells were thought to be degenerate cells. The significance of these findings is discussed in relation to the nature of alpha-chain disease and immunoproliferative small intestinal disease in general.

摘要

对α链病小肠中的浆细胞浸润进行了超微结构研究,以确定是否存在明显的核质不同步,即使在疾病早期,这也可作为该疾病肿瘤性质的证据。未发现这种不同步现象。在疾病早期,浸润主要是轻度未成熟的浆细胞,与乳糜泻的浆细胞难以区分。后期的特征是在深部黏膜出现分化程度较低的免疫母细胞并浸润到腺体中。多核浆细胞样细胞被认为是退化细胞。结合α链病和一般免疫增殖性小肠疾病的性质,讨论了这些发现的意义。

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