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Promyelocytic Sarcoma of the Spine: A Case Report and Review of the Literature

Myeloid sarcoma (MS, previously named granulocytic sarcoma or chloroma) is a rare extramedullary tumour of immature myeloid cells. It can be present before, concurrently with, or after the diagnosis of acute myeloid leukemia. MS is extremely uncommon in acute promyelocytic leukemia (APL). In the cas...

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Autores principales: Pacilli, Leonardo, Lo Coco, Francesco, Ramadan, Safaa Mahmoud, Giannì, Laura, Pingi, Alberto, Remotti, Daniele, Majolino, Ignazio
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2843861/
https://www.ncbi.nlm.nih.gov/pubmed/20339529
http://dx.doi.org/10.1155/2010/137608
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author Pacilli, Leonardo
Lo Coco, Francesco
Ramadan, Safaa Mahmoud
Giannì, Laura
Pingi, Alberto
Remotti, Daniele
Majolino, Ignazio
author_facet Pacilli, Leonardo
Lo Coco, Francesco
Ramadan, Safaa Mahmoud
Giannì, Laura
Pingi, Alberto
Remotti, Daniele
Majolino, Ignazio
author_sort Pacilli, Leonardo
collection PubMed
description Myeloid sarcoma (MS, previously named granulocytic sarcoma or chloroma) is a rare extramedullary tumour of immature myeloid cells. It can be present before, concurrently with, or after the diagnosis of acute myeloid leukemia. MS is extremely uncommon in acute promyelocytic leukemia (APL). In the case described here, MS was the sole site of APL relapse and the cause of spinal cord compression. The patient presented with neurologic symptoms due to a paravertebral mass of MS after 7 years of complete remission. He was treated with excision of the mass followed by local radiotherapy. Systemic treatment was also given with combined arsenic trioxide and all-trans retinoic acid and the patient was able to achieve a second prolonged clinical and molecular remission.
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spelling pubmed-28438612010-03-25 Promyelocytic Sarcoma of the Spine: A Case Report and Review of the Literature Pacilli, Leonardo Lo Coco, Francesco Ramadan, Safaa Mahmoud Giannì, Laura Pingi, Alberto Remotti, Daniele Majolino, Ignazio Adv Hematol Case Report Myeloid sarcoma (MS, previously named granulocytic sarcoma or chloroma) is a rare extramedullary tumour of immature myeloid cells. It can be present before, concurrently with, or after the diagnosis of acute myeloid leukemia. MS is extremely uncommon in acute promyelocytic leukemia (APL). In the case described here, MS was the sole site of APL relapse and the cause of spinal cord compression. The patient presented with neurologic symptoms due to a paravertebral mass of MS after 7 years of complete remission. He was treated with excision of the mass followed by local radiotherapy. Systemic treatment was also given with combined arsenic trioxide and all-trans retinoic acid and the patient was able to achieve a second prolonged clinical and molecular remission. Hindawi Publishing Corporation 2010 2010-03-18 /pmc/articles/PMC2843861/ /pubmed/20339529 http://dx.doi.org/10.1155/2010/137608 Text en Copyright © 2010 Leonardo Pacilli et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Pacilli, Leonardo
Lo Coco, Francesco
Ramadan, Safaa Mahmoud
Giannì, Laura
Pingi, Alberto
Remotti, Daniele
Majolino, Ignazio
Promyelocytic Sarcoma of the Spine: A Case Report and Review of the Literature
title Promyelocytic Sarcoma of the Spine: A Case Report and Review of the Literature
title_full Promyelocytic Sarcoma of the Spine: A Case Report and Review of the Literature
title_fullStr Promyelocytic Sarcoma of the Spine: A Case Report and Review of the Literature
title_full_unstemmed Promyelocytic Sarcoma of the Spine: A Case Report and Review of the Literature
title_short Promyelocytic Sarcoma of the Spine: A Case Report and Review of the Literature
title_sort promyelocytic sarcoma of the spine: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2843861/
https://www.ncbi.nlm.nih.gov/pubmed/20339529
http://dx.doi.org/10.1155/2010/137608
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