Chaudhry A P, Satchidanand S K, Anthone R, Baumler R A, Gaeta J F
J Pathol. 1980 Jul;131(3):193-208. doi: 10.1002/path.1711310302.
A case of malakoplakia of the supraclavicular region and colon in a 41-year-old patient is presented. Clinical, histopathological, histochemical and ultrastructural features are described. The etiology and pathogenesis are discussed. Malakoplakia is a chronic inflammatory disorder probably due to an abnormal response to infection with Gram negative bacteria, most likely Escherichia coli or Klebsiella. The disease is characterised by the accumulation of macrophages intermixed with plasma cells and lymphocytes. The malakoplakic cells are laden with phagolysosomes which may provide a suitable biochemical environment for the deposition of calcium to form the pathognomonic Michaelis-Gutmann bodies. Ultrastructural examination enhances the accuracy of diagnosis since it highlights the presence of lysosomes, phagolysosomes, Michaelis-Gutmann bodies, and intact E. coli or their remnants.
本文报告了一例41岁患者锁骨上区域和结肠发生软斑病的病例。描述了其临床、组织病理学、组织化学和超微结构特征。对病因和发病机制进行了讨论。软斑病是一种慢性炎症性疾病,可能是由于对革兰氏阴性菌感染的异常反应所致,最常见的是大肠杆菌或克雷伯菌。该病的特征是巨噬细胞与浆细胞和淋巴细胞混合积聚。软斑病细胞内充满吞噬溶酶体,这可能为钙沉积形成特征性的米氏小体提供了合适的生化环境。超微结构检查提高了诊断的准确性,因为它突出了溶酶体、吞噬溶酶体、米氏小体以及完整的大肠杆菌或其残余物的存在。