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米氏-古特曼小体的组织化学特征及其形成的病理生理机制探讨。

The histochemical features of the Michaelis-Gutmann body and a consideration of the pathophysiological mechanisms of its formation.

作者信息

Stevens S, McClure J

出版信息

J Pathol. 1982 Jun;137(2):119-27. doi: 10.1002/path.1711370205.

Abstract

The reactions to a number of histochemical stains by Michaelis-Gutmann (MG) bodies in 13 cases of malakoplakia are described. All MG bodies contained calcium and phosphate. Iron was present in six cases. Special stains failed to reveal the presence of micro-organisms. In six cases the MG bodies contained either lecithin or sphingomyelin and in three both phospholipids were present. There was no evidence of phospholipid of bacterial cell membrane derivation. Carbohydrate staining reactions suggested the presence of a neutral polysaccharide and an acidic non-sulphated polysaccharide (such as a sialoglycan). No histochemical evidence could be adduced to implicate bacterial cell membranes in the structure of the organic matrix of the MG body. The implications of these findings in the light of the association between clinical bacterial infection and malakoplakia are discussed.

摘要

本文描述了13例软斑病中米氏-古特曼(MG)小体对多种组织化学染色的反应。所有MG小体均含有钙和磷酸盐。6例中存在铁。特殊染色未显示微生物的存在。6例中MG小体含有卵磷脂或鞘磷脂,3例中两种磷脂均存在。没有证据表明存在源自细菌细胞膜的磷脂。碳水化合物染色反应提示存在中性多糖和酸性非硫酸化多糖(如唾液酸聚糖)。没有组织化学证据表明细菌细胞膜与MG小体有机基质的结构有关。根据临床细菌感染与软斑病之间的关联,讨论了这些发现的意义。

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