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Micro-CT evaluation of historical human skulls presenting signs of syphilitic infection
BACKGROUND: In tertiary syphilis, Treponema pallidum triggers the formation of granulomatous nodules in various organs of the human body. Within the skeleton, predominantly in the skull and long bones, these characteristic syphilitic lesions cause typical patterns of bone damage. In this study, micr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195897/ https://www.ncbi.nlm.nih.gov/pubmed/33791870 http://dx.doi.org/10.1007/s00508-021-01832-z |
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author | Fraberger, Sabine Dockner, Martin Winter, Eduard Pretterklieber, Michael Weber, Gerhard W. Teschler-Nicola, Maria Pietschmann, Peter |
author_facet | Fraberger, Sabine Dockner, Martin Winter, Eduard Pretterklieber, Michael Weber, Gerhard W. Teschler-Nicola, Maria Pietschmann, Peter |
author_sort | Fraberger, Sabine |
collection | PubMed |
description | BACKGROUND: In tertiary syphilis, Treponema pallidum triggers the formation of granulomatous nodules in various organs of the human body. Within the skeleton, predominantly in the skull and long bones, these characteristic syphilitic lesions cause typical patterns of bone damage. In this study, micro-computed tomography (µ-CT) was used to assess the microarchitecture of these osseous defects in untreated syphilitic skull bones. MATERIAL AND METHODS: Bone structure of 30 macerated human skulls was noninvasively examined by means of µ-CT images (Viscom X8060 NDT). A total of 20 specimens showing typical morphological signs of syphilis were provided by the Collection of Anatomical Pathology of the Museum of Natural History in Vienna. They were compared to 10 macerated control skulls provided by the Division of Anatomy of the Medical University of Vienna. RESULTS: All samples affected by syphilis showed perforating defects and increased porosity. Furthermore, we observed sclerotic reorganization and complete loss of the cortical bone in 80% of infected cases. Cortical thinning occurred in 75%. CONCLUSION: Our findings revealed extensive micromorphological bone destruction and a broad variability of osseous manifestations of (tertiary) syphilis. |
format | Online Article Text |
id | pubmed-8195897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-81958972021-06-28 Micro-CT evaluation of historical human skulls presenting signs of syphilitic infection Fraberger, Sabine Dockner, Martin Winter, Eduard Pretterklieber, Michael Weber, Gerhard W. Teschler-Nicola, Maria Pietschmann, Peter Wien Klin Wochenschr Original Article BACKGROUND: In tertiary syphilis, Treponema pallidum triggers the formation of granulomatous nodules in various organs of the human body. Within the skeleton, predominantly in the skull and long bones, these characteristic syphilitic lesions cause typical patterns of bone damage. In this study, micro-computed tomography (µ-CT) was used to assess the microarchitecture of these osseous defects in untreated syphilitic skull bones. MATERIAL AND METHODS: Bone structure of 30 macerated human skulls was noninvasively examined by means of µ-CT images (Viscom X8060 NDT). A total of 20 specimens showing typical morphological signs of syphilis were provided by the Collection of Anatomical Pathology of the Museum of Natural History in Vienna. They were compared to 10 macerated control skulls provided by the Division of Anatomy of the Medical University of Vienna. RESULTS: All samples affected by syphilis showed perforating defects and increased porosity. Furthermore, we observed sclerotic reorganization and complete loss of the cortical bone in 80% of infected cases. Cortical thinning occurred in 75%. CONCLUSION: Our findings revealed extensive micromorphological bone destruction and a broad variability of osseous manifestations of (tertiary) syphilis. Springer Vienna 2021-03-31 2021 /pmc/articles/PMC8195897/ /pubmed/33791870 http://dx.doi.org/10.1007/s00508-021-01832-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Fraberger, Sabine Dockner, Martin Winter, Eduard Pretterklieber, Michael Weber, Gerhard W. Teschler-Nicola, Maria Pietschmann, Peter Micro-CT evaluation of historical human skulls presenting signs of syphilitic infection |
title | Micro-CT evaluation of historical human skulls presenting signs of syphilitic infection |
title_full | Micro-CT evaluation of historical human skulls presenting signs of syphilitic infection |
title_fullStr | Micro-CT evaluation of historical human skulls presenting signs of syphilitic infection |
title_full_unstemmed | Micro-CT evaluation of historical human skulls presenting signs of syphilitic infection |
title_short | Micro-CT evaluation of historical human skulls presenting signs of syphilitic infection |
title_sort | micro-ct evaluation of historical human skulls presenting signs of syphilitic infection |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195897/ https://www.ncbi.nlm.nih.gov/pubmed/33791870 http://dx.doi.org/10.1007/s00508-021-01832-z |
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