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Orbital myeloid sarcoma misdiagnosed for subperiostal hematoma: a case report

BACKGROUND: Myeloid sarcoma is a solid tumor that consists of immature myeloid cells occurring at an extramedullary site. It can present before, concurrent with, or after the diagnosis of acute myeloid leukemia or other myeloproliferative diseases, and a proportion of patients never develop bone mar...

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Autores principales: Razem, Bahaa, Raiteb, Mohamed, El Mrini, Sanaa, Slimani, Faiçal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501704/
https://www.ncbi.nlm.nih.gov/pubmed/34625114
http://dx.doi.org/10.1186/s13256-021-03025-8
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author Razem, Bahaa
Raiteb, Mohamed
El Mrini, Sanaa
Slimani, Faiçal
author_facet Razem, Bahaa
Raiteb, Mohamed
El Mrini, Sanaa
Slimani, Faiçal
author_sort Razem, Bahaa
collection PubMed
description BACKGROUND: Myeloid sarcoma is a solid tumor that consists of immature myeloid cells occurring at an extramedullary site. It can present before, concurrent with, or after the diagnosis of acute myeloid leukemia or other myeloproliferative diseases, and a proportion of patients never develop bone marrow infiltration. Only a few isolated cases of pediatric orbital myeloid sarcoma have been reported, and they are often associated with a high misdiagnosis rate. CASE REPORT: We report a rare case of pediatric orbital myeloid sarcoma associated with blunt trauma in a 3-year-old Caucasian male patient, which was clinically and radiologically misdiagnosed for orbital subperiostal hematoma. The patient underwent a surgical intervention to drain the hematoma when an orbital mass was found. The microscopic, immunologic, and genetic features of the tumor and the myelogram were in favor of LAM2, and the patient was started with chemotherapy with a favorable evolution within 18 months follow-up. CONCLUSION: Orbital myeloid sarcoma usually exhibits clinical and radiological features that can be easily misleading, especially if it happens de novo or as the first manifestation of acute myeloid leukemia. Only a few isolated cases have reported and proposed trauma as a trigger event of the onset of this type of tumor proliferation, but further investigations and evidence are needed to support this hypothesis.
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spelling pubmed-85017042021-10-20 Orbital myeloid sarcoma misdiagnosed for subperiostal hematoma: a case report Razem, Bahaa Raiteb, Mohamed El Mrini, Sanaa Slimani, Faiçal J Med Case Rep Case Report BACKGROUND: Myeloid sarcoma is a solid tumor that consists of immature myeloid cells occurring at an extramedullary site. It can present before, concurrent with, or after the diagnosis of acute myeloid leukemia or other myeloproliferative diseases, and a proportion of patients never develop bone marrow infiltration. Only a few isolated cases of pediatric orbital myeloid sarcoma have been reported, and they are often associated with a high misdiagnosis rate. CASE REPORT: We report a rare case of pediatric orbital myeloid sarcoma associated with blunt trauma in a 3-year-old Caucasian male patient, which was clinically and radiologically misdiagnosed for orbital subperiostal hematoma. The patient underwent a surgical intervention to drain the hematoma when an orbital mass was found. The microscopic, immunologic, and genetic features of the tumor and the myelogram were in favor of LAM2, and the patient was started with chemotherapy with a favorable evolution within 18 months follow-up. CONCLUSION: Orbital myeloid sarcoma usually exhibits clinical and radiological features that can be easily misleading, especially if it happens de novo or as the first manifestation of acute myeloid leukemia. Only a few isolated cases have reported and proposed trauma as a trigger event of the onset of this type of tumor proliferation, but further investigations and evidence are needed to support this hypothesis. BioMed Central 2021-10-08 /pmc/articles/PMC8501704/ /pubmed/34625114 http://dx.doi.org/10.1186/s13256-021-03025-8 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Razem, Bahaa
Raiteb, Mohamed
El Mrini, Sanaa
Slimani, Faiçal
Orbital myeloid sarcoma misdiagnosed for subperiostal hematoma: a case report
title Orbital myeloid sarcoma misdiagnosed for subperiostal hematoma: a case report
title_full Orbital myeloid sarcoma misdiagnosed for subperiostal hematoma: a case report
title_fullStr Orbital myeloid sarcoma misdiagnosed for subperiostal hematoma: a case report
title_full_unstemmed Orbital myeloid sarcoma misdiagnosed for subperiostal hematoma: a case report
title_short Orbital myeloid sarcoma misdiagnosed for subperiostal hematoma: a case report
title_sort orbital myeloid sarcoma misdiagnosed for subperiostal hematoma: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501704/
https://www.ncbi.nlm.nih.gov/pubmed/34625114
http://dx.doi.org/10.1186/s13256-021-03025-8
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