August C, Holzhausen H J, Schröder S
Institute of Pathology, University of Hamburg, Germany.
Ultrastruct Pathol. 1994 Sep-Oct;18(5):483-91. doi: 10.3109/01913129409023223.
Light microscopic and ultrastructural findings in five cases of renal parenchymal malakoplakia detected in renal biopsy specimens (four cases) or observed at autopsy (one case) are reported. The spectrum of ultrastructural changes ranging from lamellar and microvesicular phagolysosomal inclusions arranged in a biphasic pattern to fully developed Michaelis-Gutmann bodies is described. In three of the biopsy cases the lesions appeared to represent early stages of malakoplakia lacking classic Michaelis-Gutmann bodies. Especially in this phase of disease, ultrastructural investigation can distinguish between this condition and other histiocytic interstitial renal processes. The findings show that focal cytoplasmic degeneration and autophagolysosomal processes observed in macrophages could precede the disturbance in the process of bacterial breakdown that is responsible for the peculiar granuloma-like inflammatory histiocytic reaction.
报告了在肾活检标本(4例)中检测到或尸检时观察到(1例)的5例肾实质软斑病的光镜和超微结构结果。描述了超微结构变化的范围,从呈双相模式排列的层状和微泡状吞噬溶酶体包涵体到完全发育的迈克尔is -古特曼小体。在3例活检病例中,病变似乎代表缺乏经典迈克尔is -古特曼小体的软斑病早期阶段。特别是在疾病的这个阶段,超微结构研究可以区分这种情况与其他组织细胞性间质性肾病变。研究结果表明,巨噬细胞中观察到的局灶性细胞质变性和自噬溶酶体过程可能先于负责特殊肉芽肿样炎症组织细胞反应的细菌分解过程的紊乱。