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Spinal Intradural Extramedullary Capillary Hemangioma with Coexistent Spinal Edema and Syringomyelia Successfully Treated by Tumor Removal and Cervical Laminoplasty
Capillary hemangioma (CH) is usually found in pediatric patients and is located in soft tissue of the neck or head. As uncommon location of CH, spinal intradural extramedullary space has been reported; however, coexistent spinal edema or syringomyelia with spinal intradural extramedullary CH seems r...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751536/ https://www.ncbi.nlm.nih.gov/pubmed/35071092 http://dx.doi.org/10.4103/ajns.AJNS_51_21 |
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author | Takayama, Motohiro Maki, Yoshinori |
author_facet | Takayama, Motohiro Maki, Yoshinori |
author_sort | Takayama, Motohiro |
collection | PubMed |
description | Capillary hemangioma (CH) is usually found in pediatric patients and is located in soft tissue of the neck or head. As uncommon location of CH, spinal intradural extramedullary space has been reported; however, coexistent spinal edema or syringomyelia with spinal intradural extramedullary CH seems rare manifestations on preoperative magnetic resonance imaging. Laminectomy and tumor resection have been often performed for spinal intradural extramedullary CH. An 83-year-old man was referred to our hospital, complaining of nocturia and motor weakness of the lower extremities. Magnetic resonance imaging revealed a mass at the level of T1, which was homogeneously enhanced on gadolinium-enhanced T1-weighted images. The lesion was accompanied by spinal edema and syringomyelia. An intradural extramedullary tumor was first considered. We thought that the coexistent spinal edema and syringomyelia could have been caused by spinal stenosis. Preoperative angiography revealed that the mass was fed by the radicular artery of C5–C6. To improve the clinical symptoms of the patient, tumor removal and cervical laminoplasty were performed. The spinal edema and syringomyelia regressed postoperatively. The histopathological diagnosis was CH. This is the first reported case of cervical intradural extramedullary CH with spinal edema and syringomyelia successfully treated by cervical laminoplasty and tumor removal. |
format | Online Article Text |
id | pubmed-8751536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-87515362022-01-21 Spinal Intradural Extramedullary Capillary Hemangioma with Coexistent Spinal Edema and Syringomyelia Successfully Treated by Tumor Removal and Cervical Laminoplasty Takayama, Motohiro Maki, Yoshinori Asian J Neurosurg Case Report Capillary hemangioma (CH) is usually found in pediatric patients and is located in soft tissue of the neck or head. As uncommon location of CH, spinal intradural extramedullary space has been reported; however, coexistent spinal edema or syringomyelia with spinal intradural extramedullary CH seems rare manifestations on preoperative magnetic resonance imaging. Laminectomy and tumor resection have been often performed for spinal intradural extramedullary CH. An 83-year-old man was referred to our hospital, complaining of nocturia and motor weakness of the lower extremities. Magnetic resonance imaging revealed a mass at the level of T1, which was homogeneously enhanced on gadolinium-enhanced T1-weighted images. The lesion was accompanied by spinal edema and syringomyelia. An intradural extramedullary tumor was first considered. We thought that the coexistent spinal edema and syringomyelia could have been caused by spinal stenosis. Preoperative angiography revealed that the mass was fed by the radicular artery of C5–C6. To improve the clinical symptoms of the patient, tumor removal and cervical laminoplasty were performed. The spinal edema and syringomyelia regressed postoperatively. The histopathological diagnosis was CH. This is the first reported case of cervical intradural extramedullary CH with spinal edema and syringomyelia successfully treated by cervical laminoplasty and tumor removal. Wolters Kluwer - Medknow 2021-12-18 /pmc/articles/PMC8751536/ /pubmed/35071092 http://dx.doi.org/10.4103/ajns.AJNS_51_21 Text en Copyright: © 2021 Asian Journal of Neurosurgery https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Takayama, Motohiro Maki, Yoshinori Spinal Intradural Extramedullary Capillary Hemangioma with Coexistent Spinal Edema and Syringomyelia Successfully Treated by Tumor Removal and Cervical Laminoplasty |
title | Spinal Intradural Extramedullary Capillary Hemangioma with Coexistent Spinal Edema and Syringomyelia Successfully Treated by Tumor Removal and Cervical Laminoplasty |
title_full | Spinal Intradural Extramedullary Capillary Hemangioma with Coexistent Spinal Edema and Syringomyelia Successfully Treated by Tumor Removal and Cervical Laminoplasty |
title_fullStr | Spinal Intradural Extramedullary Capillary Hemangioma with Coexistent Spinal Edema and Syringomyelia Successfully Treated by Tumor Removal and Cervical Laminoplasty |
title_full_unstemmed | Spinal Intradural Extramedullary Capillary Hemangioma with Coexistent Spinal Edema and Syringomyelia Successfully Treated by Tumor Removal and Cervical Laminoplasty |
title_short | Spinal Intradural Extramedullary Capillary Hemangioma with Coexistent Spinal Edema and Syringomyelia Successfully Treated by Tumor Removal and Cervical Laminoplasty |
title_sort | spinal intradural extramedullary capillary hemangioma with coexistent spinal edema and syringomyelia successfully treated by tumor removal and cervical laminoplasty |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751536/ https://www.ncbi.nlm.nih.gov/pubmed/35071092 http://dx.doi.org/10.4103/ajns.AJNS_51_21 |
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