4.6 Article

Monkeypox: A Histopathological and Transmission Electron Microscopy Study

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MICROORGANISMS
卷 11, 期 7, 页码 -

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MDPI
DOI: 10.3390/microorganisms11071781

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monkeypox; virology; cutaneous manifestations; histopathology; transmission electron microscopy

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The global outbreak of human monkeypox virus in 2022 emphasized the importance of dermatological manifestations for its diagnosis. This study analyzed skin biopsies to assess the histopathological and microscopic findings of cutaneous lesions related to hMPXV infection. The findings provided valuable insights into the disease's histological and microscopic characteristics, contributing to a better understanding of the current and potential future trends of human monkeypox virus and other Orthopoxvirus infections.
The global outbreak of human monkeypox virus (hMPXV1) in 2022 highlighted the usefulness of dermatological manifestations for its diagnosis. Infection by the human monkeypox virus thus necessitated inclusion in the diagnostic repertoire of dermatopathology. To assess the histopathological and microscopical findings of cutaneous lesions related to hMPXV infection, we analyzed skin biopsies from patients with positive MPXV DNA polymerase chain reaction presenting with a typical course of hMPXV1 infection. The most prominent histopathological findings were ascribable to a pustular stage in which epidermal necrosis with areas of non-viable keratinocytes and a shadow cell appearance were evident; in some cases, the deep portion of the hair follicle and the acrosyringial epithelium were affected. The main cytopathic modifications included ballooning keratinocytes, followed by Guarnieri bodies and a ground glass appearance of the keratinocytes' nuclei, together with a dense mixed inflammatory cell infiltrate with prominent neutrophil exocytosis. Transmission electron microscopy analysis demonstrated viral particle aggregates in the cytoplasm of keratinocytes, without any involvement of the nucleus. Interestingly, we also found the presence of viral particles in infected mesenchymal cells, although to a lesser extent than in epithelial cells. Through this study, we contributed to expanding the histological and microscopic knowledge of the human mpox virus, a key step to understanding current and potential future trends of the disease, as well as of other Orthopoxvirus infections.

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