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Granulocytic sarcoma presenting as presenting as monoparesis: A rare case report

Granulocytic sarcomas (GSs) or myeloid sarcoma or chloroma are rare, destructive, extramedullary tumor masses that consist of immature granulocytic cells. We present case of a 35-year-old man presenting as monoparesis, diagnosed to have cervical intradural extramedullary mass lesion with an extradur...

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Autores principales: Gupta, Ashok, Chanduka, Amit, Sundar, I. Vijay, Verma, Jitender, Chopra, Sanjeev
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323979/
https://www.ncbi.nlm.nih.gov/pubmed/25685232
http://dx.doi.org/10.4103/1793-5482.146641
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author Gupta, Ashok
Chanduka, Amit
Sundar, I. Vijay
Verma, Jitender
Chopra, Sanjeev
author_facet Gupta, Ashok
Chanduka, Amit
Sundar, I. Vijay
Verma, Jitender
Chopra, Sanjeev
author_sort Gupta, Ashok
collection PubMed
description Granulocytic sarcomas (GSs) or myeloid sarcoma or chloroma are rare, destructive, extramedullary tumor masses that consist of immature granulocytic cells. We present case of a 35-year-old man presenting as monoparesis, diagnosed to have cervical intradural extramedullary mass lesion with an extradural extension. Although the history or physical examination had no symptoms and signs suggestive of leukemia, bone marrow study and blood picture indicated chronic myeloid leukemia. Surgical decompression was done, and histopathological examination was consistent with GS. GSs have been observed in patients with acute myelogenous leukemia, chronic myelogenous leukemia, and other myeloproliferative disorders, but rarely have been reported as first presentation of the disease.
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spelling pubmed-43239792015-02-13 Granulocytic sarcoma presenting as presenting as monoparesis: A rare case report Gupta, Ashok Chanduka, Amit Sundar, I. Vijay Verma, Jitender Chopra, Sanjeev Asian J Neurosurg Case Report Granulocytic sarcomas (GSs) or myeloid sarcoma or chloroma are rare, destructive, extramedullary tumor masses that consist of immature granulocytic cells. We present case of a 35-year-old man presenting as monoparesis, diagnosed to have cervical intradural extramedullary mass lesion with an extradural extension. Although the history or physical examination had no symptoms and signs suggestive of leukemia, bone marrow study and blood picture indicated chronic myeloid leukemia. Surgical decompression was done, and histopathological examination was consistent with GS. GSs have been observed in patients with acute myelogenous leukemia, chronic myelogenous leukemia, and other myeloproliferative disorders, but rarely have been reported as first presentation of the disease. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4323979/ /pubmed/25685232 http://dx.doi.org/10.4103/1793-5482.146641 Text en Copyright: © Asian Journal of Neurosurgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Gupta, Ashok
Chanduka, Amit
Sundar, I. Vijay
Verma, Jitender
Chopra, Sanjeev
Granulocytic sarcoma presenting as presenting as monoparesis: A rare case report
title Granulocytic sarcoma presenting as presenting as monoparesis: A rare case report
title_full Granulocytic sarcoma presenting as presenting as monoparesis: A rare case report
title_fullStr Granulocytic sarcoma presenting as presenting as monoparesis: A rare case report
title_full_unstemmed Granulocytic sarcoma presenting as presenting as monoparesis: A rare case report
title_short Granulocytic sarcoma presenting as presenting as monoparesis: A rare case report
title_sort granulocytic sarcoma presenting as presenting as monoparesis: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323979/
https://www.ncbi.nlm.nih.gov/pubmed/25685232
http://dx.doi.org/10.4103/1793-5482.146641
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