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An Uncommon Intramedullary Tumor: Primary Spinal Cord Melanoma

A 47-year-old woman was admitted with complaints of progressive weakness in the lower extremities and pain in the back and left leg. Thoracic magnetic resonance imaging (MRI) revealed a spinal intramedullary tumor between the T9 and L1 levels, which were iso- to hypointense on T2 and slightly hyperi...

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Autores principales: Çetinalp, Nuri Eralp, Yildirim, Ali Erdem, Divanlioglu, Denizhan, Belen, Deniz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Spine Surgery 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149997/
https://www.ncbi.nlm.nih.gov/pubmed/25187871
http://dx.doi.org/10.4184/asj.2014.8.4.512
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author Çetinalp, Nuri Eralp
Yildirim, Ali Erdem
Divanlioglu, Denizhan
Belen, Deniz
author_facet Çetinalp, Nuri Eralp
Yildirim, Ali Erdem
Divanlioglu, Denizhan
Belen, Deniz
author_sort Çetinalp, Nuri Eralp
collection PubMed
description A 47-year-old woman was admitted with complaints of progressive weakness in the lower extremities and pain in the back and left leg. Thoracic magnetic resonance imaging (MRI) revealed a spinal intramedullary tumor between the T9 and L1 levels, which were iso- to hypointense on T2 and slightly hyperintense on T1-weighted images. The tumor was resected as total, and the diagnosis was malignant melanoma confirmed with histopathology. Neurological findings improved at the postoperative period and no residual or recurrence was noted on postoperative MRI at the 9-month follow-up. Primary melanoma of the spinal cord, particularly intramedullar localization, is seldomly reported in the literature. We report a primary malignant melanoma of the spinal cord and emphasize the diagnostic and prognostic challenges.
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spelling pubmed-41499972014-09-03 An Uncommon Intramedullary Tumor: Primary Spinal Cord Melanoma Çetinalp, Nuri Eralp Yildirim, Ali Erdem Divanlioglu, Denizhan Belen, Deniz Asian Spine J Case Report A 47-year-old woman was admitted with complaints of progressive weakness in the lower extremities and pain in the back and left leg. Thoracic magnetic resonance imaging (MRI) revealed a spinal intramedullary tumor between the T9 and L1 levels, which were iso- to hypointense on T2 and slightly hyperintense on T1-weighted images. The tumor was resected as total, and the diagnosis was malignant melanoma confirmed with histopathology. Neurological findings improved at the postoperative period and no residual or recurrence was noted on postoperative MRI at the 9-month follow-up. Primary melanoma of the spinal cord, particularly intramedullar localization, is seldomly reported in the literature. We report a primary malignant melanoma of the spinal cord and emphasize the diagnostic and prognostic challenges. Korean Society of Spine Surgery 2014-08 2014-08-19 /pmc/articles/PMC4149997/ /pubmed/25187871 http://dx.doi.org/10.4184/asj.2014.8.4.512 Text en Copyright © 2014 by Korean Society of Spine Surgery http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Çetinalp, Nuri Eralp
Yildirim, Ali Erdem
Divanlioglu, Denizhan
Belen, Deniz
An Uncommon Intramedullary Tumor: Primary Spinal Cord Melanoma
title An Uncommon Intramedullary Tumor: Primary Spinal Cord Melanoma
title_full An Uncommon Intramedullary Tumor: Primary Spinal Cord Melanoma
title_fullStr An Uncommon Intramedullary Tumor: Primary Spinal Cord Melanoma
title_full_unstemmed An Uncommon Intramedullary Tumor: Primary Spinal Cord Melanoma
title_short An Uncommon Intramedullary Tumor: Primary Spinal Cord Melanoma
title_sort uncommon intramedullary tumor: primary spinal cord melanoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149997/
https://www.ncbi.nlm.nih.gov/pubmed/25187871
http://dx.doi.org/10.4184/asj.2014.8.4.512
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