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Intracranial Myeloid Sarcoma Mimicking Hypertensive Intracerebral Hemorrhage

We herein report a case of intracranial myeloid sarcoma mimicking hypertensive intracerebral hemorrhage. A 71-year-old man with a history of acute myeloid leukemia was admitted with acute-onset dysarthria. A hematoma-like lesion was found on computed tomography in the left putamen. Magnetic resonanc...

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Autores principales: Ikeda, Shuhei, Tsutsumi, Masaomi, Fujita, Mai, Okamoto, Sho, Eriguchi, Makoto, Hara, Hideo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518558/
https://www.ncbi.nlm.nih.gov/pubmed/36725032
http://dx.doi.org/10.2169/internalmedicine.9774-22
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author Ikeda, Shuhei
Tsutsumi, Masaomi
Fujita, Mai
Okamoto, Sho
Eriguchi, Makoto
Hara, Hideo
author_facet Ikeda, Shuhei
Tsutsumi, Masaomi
Fujita, Mai
Okamoto, Sho
Eriguchi, Makoto
Hara, Hideo
author_sort Ikeda, Shuhei
collection PubMed
description We herein report a case of intracranial myeloid sarcoma mimicking hypertensive intracerebral hemorrhage. A 71-year-old man with a history of acute myeloid leukemia was admitted with acute-onset dysarthria. A hematoma-like lesion was found on computed tomography in the left putamen. Magnetic resonance imaging (MRI) and cerebrospinal fluid cytology confirmed the diagnosis of intracranial myeloid sarcoma. The patient showed a favorable response to chemotherapy, and follow-up MRI revealed shrinkage of the tumor. Since the computed tomography findings resemble those of intracerebral hemorrhage, it is important to suspect intracranial neoplasm, particularly in cases with a history of hematologic diseases.
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spelling pubmed-105185582023-09-26 Intracranial Myeloid Sarcoma Mimicking Hypertensive Intracerebral Hemorrhage Ikeda, Shuhei Tsutsumi, Masaomi Fujita, Mai Okamoto, Sho Eriguchi, Makoto Hara, Hideo Intern Med Case Report We herein report a case of intracranial myeloid sarcoma mimicking hypertensive intracerebral hemorrhage. A 71-year-old man with a history of acute myeloid leukemia was admitted with acute-onset dysarthria. A hematoma-like lesion was found on computed tomography in the left putamen. Magnetic resonance imaging (MRI) and cerebrospinal fluid cytology confirmed the diagnosis of intracranial myeloid sarcoma. The patient showed a favorable response to chemotherapy, and follow-up MRI revealed shrinkage of the tumor. Since the computed tomography findings resemble those of intracerebral hemorrhage, it is important to suspect intracranial neoplasm, particularly in cases with a history of hematologic diseases. The Japanese Society of Internal Medicine 2023-02-01 2023-09-01 /pmc/articles/PMC10518558/ /pubmed/36725032 http://dx.doi.org/10.2169/internalmedicine.9774-22 Text en Copyright © 2023 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Ikeda, Shuhei
Tsutsumi, Masaomi
Fujita, Mai
Okamoto, Sho
Eriguchi, Makoto
Hara, Hideo
Intracranial Myeloid Sarcoma Mimicking Hypertensive Intracerebral Hemorrhage
title Intracranial Myeloid Sarcoma Mimicking Hypertensive Intracerebral Hemorrhage
title_full Intracranial Myeloid Sarcoma Mimicking Hypertensive Intracerebral Hemorrhage
title_fullStr Intracranial Myeloid Sarcoma Mimicking Hypertensive Intracerebral Hemorrhage
title_full_unstemmed Intracranial Myeloid Sarcoma Mimicking Hypertensive Intracerebral Hemorrhage
title_short Intracranial Myeloid Sarcoma Mimicking Hypertensive Intracerebral Hemorrhage
title_sort intracranial myeloid sarcoma mimicking hypertensive intracerebral hemorrhage
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518558/
https://www.ncbi.nlm.nih.gov/pubmed/36725032
http://dx.doi.org/10.2169/internalmedicine.9774-22
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