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A rare cause of neurological deterioration to complete paraplegia after surgery for thoracic myelopathy: a case report
INTRODUCTION: Progressive deterioration of neurological status post-thoracic myelopathy surgery after a clinically stable period is rare and can pose a diagnostic dilemma. We present our experience with such a case where all known etiologies were ruled out and the cause of deterioration could not be...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6786435/ https://www.ncbi.nlm.nih.gov/pubmed/31632713 http://dx.doi.org/10.1038/s41394-019-0202-z |
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author | Kalidindi, Kalyan Kumar Varma Gupta, Mayank Chhabra, Harvinder Singh |
author_facet | Kalidindi, Kalyan Kumar Varma Gupta, Mayank Chhabra, Harvinder Singh |
author_sort | Kalidindi, Kalyan Kumar Varma |
collection | PubMed |
description | INTRODUCTION: Progressive deterioration of neurological status post-thoracic myelopathy surgery after a clinically stable period is rare and can pose a diagnostic dilemma. We present our experience with such a case where all known etiologies were ruled out and the cause of deterioration could not be conclusively identified. The course was found to be similar to sub-acute post-traumatic ascending myelopathy (SPAM). However, the condition has only been described for traumatic injuries so far. CASE PRESENTATION: Our patient presented a history of back pain and associated gait instability for one and a half months. There was no history of trauma. Investigations suggested an Anderson-like lesion at T11–T12 with cord edema at the same level suggestive of instability. She underwent posterior stabilization T9 to L2 and laminectomy of T11 as well as T12 under neuromonitoring. The postoperative sequence of events included an episode of pyrexia on the fifth day of surgery, neurological deterioration from the seventh day of surgery proceeding to complete paraplegia by the fourteenth day, no response to steroid treatment and no signs of recovery till two years post surgery. MRI findings were suggestive of SPAM, and there was no evidence of infection. DISCUSSION: Ascending myelopathy is a potential but rare cause of delayed deterioration in neurological status after surgical intervention. MRI findings of cord edema extending more than four levels above the involved segments is a characteristic finding of the condition. Ascending myelopathy may lead to complete cord injury. The precise cause of the condition is unknown and prognosis remains poor. |
format | Online Article Text |
id | pubmed-6786435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67864352020-06-05 A rare cause of neurological deterioration to complete paraplegia after surgery for thoracic myelopathy: a case report Kalidindi, Kalyan Kumar Varma Gupta, Mayank Chhabra, Harvinder Singh Spinal Cord Ser Cases Case Report INTRODUCTION: Progressive deterioration of neurological status post-thoracic myelopathy surgery after a clinically stable period is rare and can pose a diagnostic dilemma. We present our experience with such a case where all known etiologies were ruled out and the cause of deterioration could not be conclusively identified. The course was found to be similar to sub-acute post-traumatic ascending myelopathy (SPAM). However, the condition has only been described for traumatic injuries so far. CASE PRESENTATION: Our patient presented a history of back pain and associated gait instability for one and a half months. There was no history of trauma. Investigations suggested an Anderson-like lesion at T11–T12 with cord edema at the same level suggestive of instability. She underwent posterior stabilization T9 to L2 and laminectomy of T11 as well as T12 under neuromonitoring. The postoperative sequence of events included an episode of pyrexia on the fifth day of surgery, neurological deterioration from the seventh day of surgery proceeding to complete paraplegia by the fourteenth day, no response to steroid treatment and no signs of recovery till two years post surgery. MRI findings were suggestive of SPAM, and there was no evidence of infection. DISCUSSION: Ascending myelopathy is a potential but rare cause of delayed deterioration in neurological status after surgical intervention. MRI findings of cord edema extending more than four levels above the involved segments is a characteristic finding of the condition. Ascending myelopathy may lead to complete cord injury. The precise cause of the condition is unknown and prognosis remains poor. Nature Publishing Group UK 2019-06-05 /pmc/articles/PMC6786435/ /pubmed/31632713 http://dx.doi.org/10.1038/s41394-019-0202-z Text en © International Spinal Cord Society 2019 |
spellingShingle | Case Report Kalidindi, Kalyan Kumar Varma Gupta, Mayank Chhabra, Harvinder Singh A rare cause of neurological deterioration to complete paraplegia after surgery for thoracic myelopathy: a case report |
title | A rare cause of neurological deterioration to complete paraplegia after surgery for thoracic myelopathy: a case report |
title_full | A rare cause of neurological deterioration to complete paraplegia after surgery for thoracic myelopathy: a case report |
title_fullStr | A rare cause of neurological deterioration to complete paraplegia after surgery for thoracic myelopathy: a case report |
title_full_unstemmed | A rare cause of neurological deterioration to complete paraplegia after surgery for thoracic myelopathy: a case report |
title_short | A rare cause of neurological deterioration to complete paraplegia after surgery for thoracic myelopathy: a case report |
title_sort | rare cause of neurological deterioration to complete paraplegia after surgery for thoracic myelopathy: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6786435/ https://www.ncbi.nlm.nih.gov/pubmed/31632713 http://dx.doi.org/10.1038/s41394-019-0202-z |
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