囊性包虫病
阿苯达唑
病理
多房棘球绦虫
包虫病
细粒棘球绦虫
染色
生物
组织病理学
寄生虫寄主
活力测定
苏木精
医学
体外
动物
生物化学
万维网
计算机科学
作者
Selina Robers,Michael Reinehr,Lillemor Haibach,Eva Furrer,Annina Cincera,Philipp A. Kronenberg,Ramon M. Eichenberger,Peter Deplazes,Ansgar Deibel,Beat Müllhaupt,Achim Weber
摘要
Aims Infections by the larval stage of the tape worms Echinococcus multilocularis and Echinococcus granulosus s.l . are potentially fatal zoonoses affecting humans as dead‐end hosts. Histopathological evaluation of hepatic echinococcosis is an integral part of patient management, including the distinction between alveolar (AE) and cystic echinococcosis (CE), which are associated with different disease courses and treatments. To improve histopathological assessment of Echinococcus lesions, we aimed to develop robust criteria to evaluate their viability and decay. Methods and results Histomorphological criteria for determining parasitic viability based on the morphology of parasite structures and different stages of their decay were defined based on a clinically and molecularly defined cohort comprising 138 specimens from 112 patients (59 AE and 53 CE); 618 AE lesions were assessed for histopathological viability comparing haematoxylin and eosin (H&E) staining with mAbEm18 and mAbEm2G11 immunostaining. Moreover, parasite viability was systematically mapped in cross‐sections of five additional AE lesions. Protoscoleces in CE and AE displayed variable states of degeneration. Albendazole had no significant effect on the morphology of parasite structures. Viability assessment revealed high agreement between H&E and mAbEm18, but not mAbEm2G11 staining, suggesting mAbEm18 staining as reliable for parasite viability assessment. H&E and mAbEm18 staining displayed a central–peripheral gradient of parasite viability and decay across parasitic lesions, with decayed cystic lesions located more towards the lesion centre while the most viable cystic lesions were located more peripherally. Conclusions Histopathological criteria corroborated by mAbEm18 staining provide a simple and reliable tool to assess the viability of AE lesions, knowledge of which is a valuable decision‐making tool for further treatment.
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