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Giant Invasive Sacral Schwannoma Showing Chromosomal Numerical Aberrations [-14,+18,+22]

Here, we report on a rare case of a giant invasive sacral schwannoma. The patient was a 58-year-old woman who had a 6-year history of non-specific buttock pain. Histological investigation confirmed the diagnosis of cellular schwannoma. The following numerical aberration was detected using the GTG-ba...

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Autores principales: Kanamori, Masahiko, Yasuda, Taketoshi, Hori, Takeshi, Suzuki, Kayo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Spine Surgery 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779776/
https://www.ncbi.nlm.nih.gov/pubmed/24066220
http://dx.doi.org/10.4184/asj.2013.7.3.227
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author Kanamori, Masahiko
Yasuda, Taketoshi
Hori, Takeshi
Suzuki, Kayo
author_facet Kanamori, Masahiko
Yasuda, Taketoshi
Hori, Takeshi
Suzuki, Kayo
author_sort Kanamori, Masahiko
collection PubMed
description Here, we report on a rare case of a giant invasive sacral schwannoma. The patient was a 58-year-old woman who had a 6-year history of non-specific buttock pain. Histological investigation confirmed the diagnosis of cellular schwannoma. The following numerical aberration was detected using the GTG-banding method for karyotypes: 47,XX,-14,+18,+22. Cytogenetic studies of schwannomas have indicated a complete or partial loss of chromosome 22 as the most common abnormality, but this case is cytogenetically rare because of the recurrence of trisomy 22.
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spelling pubmed-37797762013-09-24 Giant Invasive Sacral Schwannoma Showing Chromosomal Numerical Aberrations [-14,+18,+22] Kanamori, Masahiko Yasuda, Taketoshi Hori, Takeshi Suzuki, Kayo Asian Spine J Case Report Here, we report on a rare case of a giant invasive sacral schwannoma. The patient was a 58-year-old woman who had a 6-year history of non-specific buttock pain. Histological investigation confirmed the diagnosis of cellular schwannoma. The following numerical aberration was detected using the GTG-banding method for karyotypes: 47,XX,-14,+18,+22. Cytogenetic studies of schwannomas have indicated a complete or partial loss of chromosome 22 as the most common abnormality, but this case is cytogenetically rare because of the recurrence of trisomy 22. Korean Society of Spine Surgery 2013-09 2013-09-04 /pmc/articles/PMC3779776/ /pubmed/24066220 http://dx.doi.org/10.4184/asj.2013.7.3.227 Text en Copyright © 2013 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
Kanamori, Masahiko
Yasuda, Taketoshi
Hori, Takeshi
Suzuki, Kayo
Giant Invasive Sacral Schwannoma Showing Chromosomal Numerical Aberrations [-14,+18,+22]
title Giant Invasive Sacral Schwannoma Showing Chromosomal Numerical Aberrations [-14,+18,+22]
title_full Giant Invasive Sacral Schwannoma Showing Chromosomal Numerical Aberrations [-14,+18,+22]
title_fullStr Giant Invasive Sacral Schwannoma Showing Chromosomal Numerical Aberrations [-14,+18,+22]
title_full_unstemmed Giant Invasive Sacral Schwannoma Showing Chromosomal Numerical Aberrations [-14,+18,+22]
title_short Giant Invasive Sacral Schwannoma Showing Chromosomal Numerical Aberrations [-14,+18,+22]
title_sort giant invasive sacral schwannoma showing chromosomal numerical aberrations [-14,+18,+22]
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779776/
https://www.ncbi.nlm.nih.gov/pubmed/24066220
http://dx.doi.org/10.4184/asj.2013.7.3.227
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