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Myeloid sarcoma and pathological fracture: a case report and review of literature

Myeloid sarcoma is a rare clinical entity that presents as an isolated proliferation of leukemic cells, concurrently with or at relapse of acute myeloid leukemia (AML), myelodysplastic syndromes/neoplasms (MDS), chronic myeloid leukemia (CML), and myeloproliferative neoplasm (MPN). Myeloid sarcoma d...

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Autores principales: Takeyasu, Sho, Morita, Ken, Saito, Seitaro, Toho, Masanori, Oyama, Takashi, Obo, Takafumi, Taoka, Kazuki, Shimura, Arika, Maki, Hiroaki, Shibata, Eisuke, Watanabe, Yusuke, Suzuki, Fumio, Zhang, Liuzhe, Kobayashi, Hiroshi, Hinata, Munetoshi, Kurokawa, Mineo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673718/
https://www.ncbi.nlm.nih.gov/pubmed/37707761
http://dx.doi.org/10.1007/s12185-023-03656-1
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author Takeyasu, Sho
Morita, Ken
Saito, Seitaro
Toho, Masanori
Oyama, Takashi
Obo, Takafumi
Taoka, Kazuki
Shimura, Arika
Maki, Hiroaki
Shibata, Eisuke
Watanabe, Yusuke
Suzuki, Fumio
Zhang, Liuzhe
Kobayashi, Hiroshi
Hinata, Munetoshi
Kurokawa, Mineo
author_facet Takeyasu, Sho
Morita, Ken
Saito, Seitaro
Toho, Masanori
Oyama, Takashi
Obo, Takafumi
Taoka, Kazuki
Shimura, Arika
Maki, Hiroaki
Shibata, Eisuke
Watanabe, Yusuke
Suzuki, Fumio
Zhang, Liuzhe
Kobayashi, Hiroshi
Hinata, Munetoshi
Kurokawa, Mineo
author_sort Takeyasu, Sho
collection PubMed
description Myeloid sarcoma is a rare clinical entity that presents as an isolated proliferation of leukemic cells, concurrently with or at relapse of acute myeloid leukemia (AML), myelodysplastic syndromes/neoplasms (MDS), chronic myeloid leukemia (CML), and myeloproliferative neoplasm (MPN). Myeloid sarcoma disrupts the normal architecture of its surrounding tissues. When it forms in long bones, it can cause their pathological fracture. We recently experienced a rare case of MDS presenting with myeloid sarcoma in the femur that eventually resulted in its pathological fracture. Detailed chromosomal analysis of the bone marrow cells suggested emergence of myeloid sarcoma during the fast-paced progression of MDS just after acquiring trisomy 22. A comprehensive review of previous cases of myeloid sarcoma-associated pathological fracture indicated possible involvement of structural rearrangements of chromosomes 9 and 22. Management of myeloid sarcoma should continue to improve, and clinicians should note that myeloid sarcoma with specific chromosomal alterations needs extra medical attention to prevent pathological fracture.
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spelling pubmed-106737182023-09-14 Myeloid sarcoma and pathological fracture: a case report and review of literature Takeyasu, Sho Morita, Ken Saito, Seitaro Toho, Masanori Oyama, Takashi Obo, Takafumi Taoka, Kazuki Shimura, Arika Maki, Hiroaki Shibata, Eisuke Watanabe, Yusuke Suzuki, Fumio Zhang, Liuzhe Kobayashi, Hiroshi Hinata, Munetoshi Kurokawa, Mineo Int J Hematol Case Report Myeloid sarcoma is a rare clinical entity that presents as an isolated proliferation of leukemic cells, concurrently with or at relapse of acute myeloid leukemia (AML), myelodysplastic syndromes/neoplasms (MDS), chronic myeloid leukemia (CML), and myeloproliferative neoplasm (MPN). Myeloid sarcoma disrupts the normal architecture of its surrounding tissues. When it forms in long bones, it can cause their pathological fracture. We recently experienced a rare case of MDS presenting with myeloid sarcoma in the femur that eventually resulted in its pathological fracture. Detailed chromosomal analysis of the bone marrow cells suggested emergence of myeloid sarcoma during the fast-paced progression of MDS just after acquiring trisomy 22. A comprehensive review of previous cases of myeloid sarcoma-associated pathological fracture indicated possible involvement of structural rearrangements of chromosomes 9 and 22. Management of myeloid sarcoma should continue to improve, and clinicians should note that myeloid sarcoma with specific chromosomal alterations needs extra medical attention to prevent pathological fracture. Springer Nature Singapore 2023-09-14 2023 /pmc/articles/PMC10673718/ /pubmed/37707761 http://dx.doi.org/10.1007/s12185-023-03656-1 Text en © The Author(s) 2023 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 Case Report
Takeyasu, Sho
Morita, Ken
Saito, Seitaro
Toho, Masanori
Oyama, Takashi
Obo, Takafumi
Taoka, Kazuki
Shimura, Arika
Maki, Hiroaki
Shibata, Eisuke
Watanabe, Yusuke
Suzuki, Fumio
Zhang, Liuzhe
Kobayashi, Hiroshi
Hinata, Munetoshi
Kurokawa, Mineo
Myeloid sarcoma and pathological fracture: a case report and review of literature
title Myeloid sarcoma and pathological fracture: a case report and review of literature
title_full Myeloid sarcoma and pathological fracture: a case report and review of literature
title_fullStr Myeloid sarcoma and pathological fracture: a case report and review of literature
title_full_unstemmed Myeloid sarcoma and pathological fracture: a case report and review of literature
title_short Myeloid sarcoma and pathological fracture: a case report and review of literature
title_sort myeloid sarcoma and pathological fracture: a case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673718/
https://www.ncbi.nlm.nih.gov/pubmed/37707761
http://dx.doi.org/10.1007/s12185-023-03656-1
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