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A solitary fibrous tumor with concurrent meningioma at the same site: A case report and review of the literature
The present study describes a case of a solitary fibrous tumor (SFT) concurrent with meningioma in the same anatomical region. The patient was admitted to Tianjin Huanhu Hospital (Tianjin, China) presenting with progressive eyesight impairment, dizziness and right hemiparesis. Cranial magnetic reson...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4887940/ https://www.ncbi.nlm.nih.gov/pubmed/27284369 http://dx.doi.org/10.3892/ol.2016.4486 |
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author | YAN, HUA LUO, KAI LIU, BAOLONG KANG, JIANMIN |
author_facet | YAN, HUA LUO, KAI LIU, BAOLONG KANG, JIANMIN |
author_sort | YAN, HUA |
collection | PubMed |
description | The present study describes a case of a solitary fibrous tumor (SFT) concurrent with meningioma in the same anatomical region. The patient was admitted to Tianjin Huanhu Hospital (Tianjin, China) presenting with progressive eyesight impairment, dizziness and right hemiparesis. Cranial magnetic resonance imaging revealed two primary tumors co-occurring at the same site. One lesion was a solid lesion located in the left frontal convex with homogeneous enhancement, and was closely associated with the dura mater; thus, it was suspected that the lesion was a meningioma. The second lesion was cystic and solid with an irregular shape, and was located next to the first tumor; this lesion was believed to be a hemangiopericytoma or astrocytoma. The patient underwent a left temporoparietal craniectomy and a complete excision of the two tumors was achieved. Subsequent pathological examination of the resected tissues confirmed that the two tumors were a secretory meningioma and a SFT, respectively. Immunohistochemistry is important in differentiating SFTs from other tumors. Currently, a total tumor resection is the optimal treatment strategy when managing these rare lesions, often with no requirement for adjuvant post-operative therapy; however, long-term follow-up is essential to detect any signs of recurrence. The possibility of multiple tumors should be taken into consideration when performing clinical examination. To further understand the mechanisms underlying the occurrence of multiple intracranial tumors, further research is required, alongside an increased number of case reports. |
format | Online Article Text |
id | pubmed-4887940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-48879402016-06-09 A solitary fibrous tumor with concurrent meningioma at the same site: A case report and review of the literature YAN, HUA LUO, KAI LIU, BAOLONG KANG, JIANMIN Oncol Lett Articles The present study describes a case of a solitary fibrous tumor (SFT) concurrent with meningioma in the same anatomical region. The patient was admitted to Tianjin Huanhu Hospital (Tianjin, China) presenting with progressive eyesight impairment, dizziness and right hemiparesis. Cranial magnetic resonance imaging revealed two primary tumors co-occurring at the same site. One lesion was a solid lesion located in the left frontal convex with homogeneous enhancement, and was closely associated with the dura mater; thus, it was suspected that the lesion was a meningioma. The second lesion was cystic and solid with an irregular shape, and was located next to the first tumor; this lesion was believed to be a hemangiopericytoma or astrocytoma. The patient underwent a left temporoparietal craniectomy and a complete excision of the two tumors was achieved. Subsequent pathological examination of the resected tissues confirmed that the two tumors were a secretory meningioma and a SFT, respectively. Immunohistochemistry is important in differentiating SFTs from other tumors. Currently, a total tumor resection is the optimal treatment strategy when managing these rare lesions, often with no requirement for adjuvant post-operative therapy; however, long-term follow-up is essential to detect any signs of recurrence. The possibility of multiple tumors should be taken into consideration when performing clinical examination. To further understand the mechanisms underlying the occurrence of multiple intracranial tumors, further research is required, alongside an increased number of case reports. D.A. Spandidos 2016-06 2016-04-20 /pmc/articles/PMC4887940/ /pubmed/27284369 http://dx.doi.org/10.3892/ol.2016.4486 Text en Copyright: © Yan et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles YAN, HUA LUO, KAI LIU, BAOLONG KANG, JIANMIN A solitary fibrous tumor with concurrent meningioma at the same site: A case report and review of the literature |
title | A solitary fibrous tumor with concurrent meningioma at the same site: A case report and review of the literature |
title_full | A solitary fibrous tumor with concurrent meningioma at the same site: A case report and review of the literature |
title_fullStr | A solitary fibrous tumor with concurrent meningioma at the same site: A case report and review of the literature |
title_full_unstemmed | A solitary fibrous tumor with concurrent meningioma at the same site: A case report and review of the literature |
title_short | A solitary fibrous tumor with concurrent meningioma at the same site: A case report and review of the literature |
title_sort | solitary fibrous tumor with concurrent meningioma at the same site: a case report and review of the literature |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4887940/ https://www.ncbi.nlm.nih.gov/pubmed/27284369 http://dx.doi.org/10.3892/ol.2016.4486 |
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