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Thoracic spinal arachnoid web and syringomyelia with rostral expansion to the first cervical spinal cord level: Case report
INTRODUCTION AND IMPORTANCE: A spinal arachnoid web is a rare pathology that has been associated with the development of syringomyelia. Syrinx expansion can occur, which can result in the development of new symptoms. In the current literature, the farthest rostral expansion of the associated syrinx...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284059/ https://www.ncbi.nlm.nih.gov/pubmed/35779315 http://dx.doi.org/10.1016/j.ijscr.2022.107360 |
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author | Nieves-Ríos, Christian Layuno-Matos, Josué G. Olivella, Gerardo Ramírez, Norman Weber-Seda, Carlos Lastra-Power, Jorge |
author_facet | Nieves-Ríos, Christian Layuno-Matos, Josué G. Olivella, Gerardo Ramírez, Norman Weber-Seda, Carlos Lastra-Power, Jorge |
author_sort | Nieves-Ríos, Christian |
collection | PubMed |
description | INTRODUCTION AND IMPORTANCE: A spinal arachnoid web is a rare pathology that has been associated with the development of syringomyelia. Syrinx expansion can occur, which can result in the development of new symptoms. In the current literature, the farthest rostral expansion of the associated syrinx has been to the C3 spinal level. CASE PRESENTATION: We present a 49-year-old Hispanic male with a thoracic spinal arachnoid web and an associated syrinx spanning from C1 to T7 spinal level. The patient developed upper extremities radicular symptoms that worsened over time. He underwent surgical management with T6–8 laminectomy and excision of the web. Postoperative follow-up evaluations demonstrated progressive clinical improvement with eventual resolution of symptoms and syringomyelia. CLINICAL DISCUSSION: Syringomyelia secondary to a thoracic spinal arachnoid web is a progressive disease that can expand rostrally to the C1 spinal level. The clinical presentation usually involves the lower extremities. However, if the upper thoracic or cervical spinal cord is involved, patients can also present symptoms in the upper extremities. Management usually involves surgical excision of the web in order to decompress the subarachnoid space and restore the normal cerebrospinal fluid (CSF) flow. CONCLUSION: Our case suggests that syringomyelia secondary to a spinal arachnoid web may continuously expand with concomitant worsening of symptoms. However, surgical resection is curative with possible remission of symptoms and normalization of spinal anatomy. |
format | Online Article Text |
id | pubmed-9284059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-92840592022-07-16 Thoracic spinal arachnoid web and syringomyelia with rostral expansion to the first cervical spinal cord level: Case report Nieves-Ríos, Christian Layuno-Matos, Josué G. Olivella, Gerardo Ramírez, Norman Weber-Seda, Carlos Lastra-Power, Jorge Int J Surg Case Rep Case Report INTRODUCTION AND IMPORTANCE: A spinal arachnoid web is a rare pathology that has been associated with the development of syringomyelia. Syrinx expansion can occur, which can result in the development of new symptoms. In the current literature, the farthest rostral expansion of the associated syrinx has been to the C3 spinal level. CASE PRESENTATION: We present a 49-year-old Hispanic male with a thoracic spinal arachnoid web and an associated syrinx spanning from C1 to T7 spinal level. The patient developed upper extremities radicular symptoms that worsened over time. He underwent surgical management with T6–8 laminectomy and excision of the web. Postoperative follow-up evaluations demonstrated progressive clinical improvement with eventual resolution of symptoms and syringomyelia. CLINICAL DISCUSSION: Syringomyelia secondary to a thoracic spinal arachnoid web is a progressive disease that can expand rostrally to the C1 spinal level. The clinical presentation usually involves the lower extremities. However, if the upper thoracic or cervical spinal cord is involved, patients can also present symptoms in the upper extremities. Management usually involves surgical excision of the web in order to decompress the subarachnoid space and restore the normal cerebrospinal fluid (CSF) flow. CONCLUSION: Our case suggests that syringomyelia secondary to a spinal arachnoid web may continuously expand with concomitant worsening of symptoms. However, surgical resection is curative with possible remission of symptoms and normalization of spinal anatomy. Elsevier 2022-06-27 /pmc/articles/PMC9284059/ /pubmed/35779315 http://dx.doi.org/10.1016/j.ijscr.2022.107360 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Nieves-Ríos, Christian Layuno-Matos, Josué G. Olivella, Gerardo Ramírez, Norman Weber-Seda, Carlos Lastra-Power, Jorge Thoracic spinal arachnoid web and syringomyelia with rostral expansion to the first cervical spinal cord level: Case report |
title | Thoracic spinal arachnoid web and syringomyelia with rostral expansion to the first cervical spinal cord level: Case report |
title_full | Thoracic spinal arachnoid web and syringomyelia with rostral expansion to the first cervical spinal cord level: Case report |
title_fullStr | Thoracic spinal arachnoid web and syringomyelia with rostral expansion to the first cervical spinal cord level: Case report |
title_full_unstemmed | Thoracic spinal arachnoid web and syringomyelia with rostral expansion to the first cervical spinal cord level: Case report |
title_short | Thoracic spinal arachnoid web and syringomyelia with rostral expansion to the first cervical spinal cord level: Case report |
title_sort | thoracic spinal arachnoid web and syringomyelia with rostral expansion to the first cervical spinal cord level: case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284059/ https://www.ncbi.nlm.nih.gov/pubmed/35779315 http://dx.doi.org/10.1016/j.ijscr.2022.107360 |
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