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SPINAL TUMORS-04 SOLITARY FIBROUS TUMOUR, A DIAGNOSTIC CONUNDRUM (A CASE REPORT)
A 33-year-old male presented with neck pain and early signs of cervical myelopathy. He had a circumferential enhancing C4 tumour with bone demineralization. He had previously had an ACDF and a biopsy of the affected region with variable histology results. Imaging revealed a circumferential C4 tumour...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10616619/ http://dx.doi.org/10.1093/noajnl/vdad121.053 |
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author | Kamande, Kenneth Cheruiyot, Davies Mukono, Samuel Fazal, Akil Waweru, Angela Cheserem, Beverly Kabethi, Penina |
author_facet | Kamande, Kenneth Cheruiyot, Davies Mukono, Samuel Fazal, Akil Waweru, Angela Cheserem, Beverly Kabethi, Penina |
author_sort | Kamande, Kenneth |
collection | PubMed |
description | A 33-year-old male presented with neck pain and early signs of cervical myelopathy. He had a circumferential enhancing C4 tumour with bone demineralization. He had previously had an ACDF and a biopsy of the affected region with variable histology results. Imaging revealed a circumferential C4 tumour with bilateral vertebral encasement and cord compression. He had an extensive tumour debulking , corpectomy and posterior fusion. His neck pain resolved and myelopathy is stable at Nurick grade I. Histology Sections showed cellular tumor composed of spindle cells with little intervening stroma CD34 positive, progesterone receptor negative and EMA. STAT6 was positive confirming a solitary fibrous tumour. Patient has commenced adjuvant radiotherapy. Solitary tumours, formerly classified hemangiopericytoma are rare. In this case, the patient had had three previous inconclusive histological evaluations. Utilization of immunohistochemistry tests enabled the establishment of a conclusive diagnosis and treatment planning. Previously solitary fibrous tumors were classified as hemangiopericytomas with the option of three grades. However, in the current 2021 WHO 5th edition, the term hemangiopericytomas has been dropped to align these tumors fully with the soft tissue pathology nomenclature. These tumors have the characteristic alteration of the NAB2-STAT6 gene/molecular profile. |
format | Online Article Text |
id | pubmed-10616619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106166192023-11-01 SPINAL TUMORS-04 SOLITARY FIBROUS TUMOUR, A DIAGNOSTIC CONUNDRUM (A CASE REPORT) Kamande, Kenneth Cheruiyot, Davies Mukono, Samuel Fazal, Akil Waweru, Angela Cheserem, Beverly Kabethi, Penina Neurooncol Adv Final Category: Spinal Tumors A 33-year-old male presented with neck pain and early signs of cervical myelopathy. He had a circumferential enhancing C4 tumour with bone demineralization. He had previously had an ACDF and a biopsy of the affected region with variable histology results. Imaging revealed a circumferential C4 tumour with bilateral vertebral encasement and cord compression. He had an extensive tumour debulking , corpectomy and posterior fusion. His neck pain resolved and myelopathy is stable at Nurick grade I. Histology Sections showed cellular tumor composed of spindle cells with little intervening stroma CD34 positive, progesterone receptor negative and EMA. STAT6 was positive confirming a solitary fibrous tumour. Patient has commenced adjuvant radiotherapy. Solitary tumours, formerly classified hemangiopericytoma are rare. In this case, the patient had had three previous inconclusive histological evaluations. Utilization of immunohistochemistry tests enabled the establishment of a conclusive diagnosis and treatment planning. Previously solitary fibrous tumors were classified as hemangiopericytomas with the option of three grades. However, in the current 2021 WHO 5th edition, the term hemangiopericytomas has been dropped to align these tumors fully with the soft tissue pathology nomenclature. These tumors have the characteristic alteration of the NAB2-STAT6 gene/molecular profile. Oxford University Press 2023-10-31 /pmc/articles/PMC10616619/ http://dx.doi.org/10.1093/noajnl/vdad121.053 Text en © The Author(s) 2023. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Final Category: Spinal Tumors Kamande, Kenneth Cheruiyot, Davies Mukono, Samuel Fazal, Akil Waweru, Angela Cheserem, Beverly Kabethi, Penina SPINAL TUMORS-04 SOLITARY FIBROUS TUMOUR, A DIAGNOSTIC CONUNDRUM (A CASE REPORT) |
title | SPINAL TUMORS-04 SOLITARY FIBROUS TUMOUR, A DIAGNOSTIC CONUNDRUM (A CASE REPORT) |
title_full | SPINAL TUMORS-04 SOLITARY FIBROUS TUMOUR, A DIAGNOSTIC CONUNDRUM (A CASE REPORT) |
title_fullStr | SPINAL TUMORS-04 SOLITARY FIBROUS TUMOUR, A DIAGNOSTIC CONUNDRUM (A CASE REPORT) |
title_full_unstemmed | SPINAL TUMORS-04 SOLITARY FIBROUS TUMOUR, A DIAGNOSTIC CONUNDRUM (A CASE REPORT) |
title_short | SPINAL TUMORS-04 SOLITARY FIBROUS TUMOUR, A DIAGNOSTIC CONUNDRUM (A CASE REPORT) |
title_sort | spinal tumors-04 solitary fibrous tumour, a diagnostic conundrum (a case report) |
topic | Final Category: Spinal Tumors |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10616619/ http://dx.doi.org/10.1093/noajnl/vdad121.053 |
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