Vitellaro-Zuccarello L, Felletti V, Paizis G, Spinelli M
Dipartimento di Fisiologia e Biochimica Generali, Sez. di Istologia ed Anatomia Umana, Milano, Italy.
Histol Histopathol. 1987 Jul;2(3):307-12.
The ultrastructural study carried out in a case of tonsillar malakoplakia confirmed that granulomatous lesions consisted mainly of macrophages containing peculiar calcified inclusions (Michaelis-Gutmann bodies) considered pathognomonic for the disease. Moreover macrophages frequently contained ingested Gram-negative bacilli and presented aspects of mitochondrial degeneration and autophagy. These latter features were probably the consequence of bacterial infection rather than the expression of primary cellular defects, as the clinical evolution of this case of malakoplakia did not support the existence of generalized macrophage alterations.
对一例扁桃体软斑病进行的超微结构研究证实,肉芽肿性病变主要由含有特殊钙化包涵体(米氏小体)的巨噬细胞组成,这些包涵体被认为是该疾病的病理特征。此外,巨噬细胞经常含有摄入的革兰氏阴性杆菌,并呈现出线粒体退化和自噬的特征。后一种特征可能是细菌感染的结果,而不是原发性细胞缺陷的表现,因为该例软斑病的临床病程不支持全身性巨噬细胞改变的存在。