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Giant cell tumor of bone in an eighteenth-century Italian mummy

Giant cell tumor (GCT) of the bone is a locally aggressive and rarely metastasizing neoplasm. It is composed of neoplastic mononuclear stromal cells with a monotonous appearance admixed with macrophages and osteoclast-like giant cells. In a small subset of cases, GCT is malignant. Terminology previo...

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Autores principales: Ventura, Luca, Petrella, Enrico, Piciucchi, Sara, Cilli, Elisabetta, Luiselli, Donata, Feeney, Robin N. M., Traversari, Mirko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8724190/
https://www.ncbi.nlm.nih.gov/pubmed/34462806
http://dx.doi.org/10.1007/s00428-021-03192-5
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author Ventura, Luca
Petrella, Enrico
Piciucchi, Sara
Cilli, Elisabetta
Luiselli, Donata
Feeney, Robin N. M.
Traversari, Mirko
author_facet Ventura, Luca
Petrella, Enrico
Piciucchi, Sara
Cilli, Elisabetta
Luiselli, Donata
Feeney, Robin N. M.
Traversari, Mirko
author_sort Ventura, Luca
collection PubMed
description Giant cell tumor (GCT) of the bone is a locally aggressive and rarely metastasizing neoplasm. It is composed of neoplastic mononuclear stromal cells with a monotonous appearance admixed with macrophages and osteoclast-like giant cells. In a small subset of cases, GCT is malignant. Terminology previously related to this entity, and which is no longer supported by the World Health Organization, includes osteoclastoma and benign fibrous histiocytoma (BFH). Giant cells occur in numerous other pathologic conditions of the bone, which accounts for the misrepresentation of these non-GCT tumors in the early literature. Non-ossifying fibroma (NOF), aneurysmal bone cyst, and chondroblastoma have been erroneously labeled GCT for this reason. A single description of an ancient GCT was reported by Brothwell and Sandison and subsequently mentioned by Aufderheide and Rodrìguez-Martìn who were astonished that more of these tumors had not been identified in archaeological cases. To the best of our knowledge, no other cases of ancient GCT have been cited in the paleopathology literature. The study of this type of neoplasm in antiquity can be used as a means to better understand its characteristics and behavior and to expand the depth of time of the etiology of these lesions. We report a case of GCT of the left femur observed following the total body CT imaging of a partially mummified adult female, dating to eighteenth century.
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spelling pubmed-87241902022-01-13 Giant cell tumor of bone in an eighteenth-century Italian mummy Ventura, Luca Petrella, Enrico Piciucchi, Sara Cilli, Elisabetta Luiselli, Donata Feeney, Robin N. M. Traversari, Mirko Virchows Arch Original Article Giant cell tumor (GCT) of the bone is a locally aggressive and rarely metastasizing neoplasm. It is composed of neoplastic mononuclear stromal cells with a monotonous appearance admixed with macrophages and osteoclast-like giant cells. In a small subset of cases, GCT is malignant. Terminology previously related to this entity, and which is no longer supported by the World Health Organization, includes osteoclastoma and benign fibrous histiocytoma (BFH). Giant cells occur in numerous other pathologic conditions of the bone, which accounts for the misrepresentation of these non-GCT tumors in the early literature. Non-ossifying fibroma (NOF), aneurysmal bone cyst, and chondroblastoma have been erroneously labeled GCT for this reason. A single description of an ancient GCT was reported by Brothwell and Sandison and subsequently mentioned by Aufderheide and Rodrìguez-Martìn who were astonished that more of these tumors had not been identified in archaeological cases. To the best of our knowledge, no other cases of ancient GCT have been cited in the paleopathology literature. The study of this type of neoplasm in antiquity can be used as a means to better understand its characteristics and behavior and to expand the depth of time of the etiology of these lesions. We report a case of GCT of the left femur observed following the total body CT imaging of a partially mummified adult female, dating to eighteenth century. Springer Berlin Heidelberg 2021-08-30 2021 /pmc/articles/PMC8724190/ /pubmed/34462806 http://dx.doi.org/10.1007/s00428-021-03192-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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
Ventura, Luca
Petrella, Enrico
Piciucchi, Sara
Cilli, Elisabetta
Luiselli, Donata
Feeney, Robin N. M.
Traversari, Mirko
Giant cell tumor of bone in an eighteenth-century Italian mummy
title Giant cell tumor of bone in an eighteenth-century Italian mummy
title_full Giant cell tumor of bone in an eighteenth-century Italian mummy
title_fullStr Giant cell tumor of bone in an eighteenth-century Italian mummy
title_full_unstemmed Giant cell tumor of bone in an eighteenth-century Italian mummy
title_short Giant cell tumor of bone in an eighteenth-century Italian mummy
title_sort giant cell tumor of bone in an eighteenth-century italian mummy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8724190/
https://www.ncbi.nlm.nih.gov/pubmed/34462806
http://dx.doi.org/10.1007/s00428-021-03192-5
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