Non‐osseous intradural tuberculoma of the thoracic spine with compressive myelopathy

Key Clinical Message An uncommon form of CNS tuberculosis called non‐osseous IDEM tuberculoma frequently results from paradoxical drug interactions. It should be considered one of the differentials when patients receiving ATT experience acute neurological impairment. Abstract Tuberculoma affecting t...

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Main Authors: Shyam Duvuru, Vivek Sanker, Syed Naureen, Gupta Prakash, Rajurkar Sanjana, Tirth Dave
Format: Article
Language:English
Published: Wiley 2023-11-01
Series:Clinical Case Reports
Subjects:
Online Access:https://doi.org/10.1002/ccr3.8131
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author Shyam Duvuru
Vivek Sanker
Syed Naureen
Gupta Prakash
Rajurkar Sanjana
Tirth Dave
author_facet Shyam Duvuru
Vivek Sanker
Syed Naureen
Gupta Prakash
Rajurkar Sanjana
Tirth Dave
author_sort Shyam Duvuru
collection DOAJ
description Key Clinical Message An uncommon form of CNS tuberculosis called non‐osseous IDEM tuberculoma frequently results from paradoxical drug interactions. It should be considered one of the differentials when patients receiving ATT experience acute neurological impairment. Abstract Tuberculoma affecting the spinal cord is a rare condition in modern times. The occurrence of non‐osseous intradural tuberculosis, specifically in the spine, is even more exceptional. In fact, it is uncommon to encounter an intradural extramedullary tuberculous granuloma that lacks radiological indications of vertebral involvement, especially within the thoracic region. We present a case of a patient with a neurological deficit caused by a non‐osseous intradural tuberculoma in the thoracic region, without any associated bone involvement. The patient experienced a gradual deterioration of neurological function. An MRI of the thoracic spine revealed the presence of a tuberculoma located intradurally, extramedullary, and juxtamedullary of the T5 vertebra. The compression of the spinal cord resulted in paraparesis which was worsening to paraplegia. A D4–D6 laminectomy and microsurgical excision were performed under intraoperative neurophysiological monitoring (IONM), and the patient showed clinical recovery. Excellent clinical outcomes were achieved. However, it is crucial to consider the possibility of a non‐osseous intradural tuberculoma as a rare condition when encountering a SOL, particularly in patients with a history of tuberculosis and spinal cord compression. In cases where a progressing neurological deficit is present, a combination of surgical intervention and anti‐tuberculous treatment should be considered as the optimal approach.
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spelling doaj.art-dafc93c2b38c4c3fbd82a6af6c28248d2023-11-28T04:14:44ZengWileyClinical Case Reports2050-09042023-11-011111n/an/a10.1002/ccr3.8131Non‐osseous intradural tuberculoma of the thoracic spine with compressive myelopathyShyam Duvuru0Vivek Sanker1Syed Naureen2Gupta Prakash3Rajurkar Sanjana4Tirth Dave5Department of Neurosurgery Apollo Specialty Hospitals Madurai Tamil Nadu IndiaTeam Erevnites Trivandrum IndiaTeam Erevnites Trivandrum IndiaTeam Erevnites Trivandrum IndiaTeam Erevnites Trivandrum IndiaTeam Erevnites Trivandrum IndiaKey Clinical Message An uncommon form of CNS tuberculosis called non‐osseous IDEM tuberculoma frequently results from paradoxical drug interactions. It should be considered one of the differentials when patients receiving ATT experience acute neurological impairment. Abstract Tuberculoma affecting the spinal cord is a rare condition in modern times. The occurrence of non‐osseous intradural tuberculosis, specifically in the spine, is even more exceptional. In fact, it is uncommon to encounter an intradural extramedullary tuberculous granuloma that lacks radiological indications of vertebral involvement, especially within the thoracic region. We present a case of a patient with a neurological deficit caused by a non‐osseous intradural tuberculoma in the thoracic region, without any associated bone involvement. The patient experienced a gradual deterioration of neurological function. An MRI of the thoracic spine revealed the presence of a tuberculoma located intradurally, extramedullary, and juxtamedullary of the T5 vertebra. The compression of the spinal cord resulted in paraparesis which was worsening to paraplegia. A D4–D6 laminectomy and microsurgical excision were performed under intraoperative neurophysiological monitoring (IONM), and the patient showed clinical recovery. Excellent clinical outcomes were achieved. However, it is crucial to consider the possibility of a non‐osseous intradural tuberculoma as a rare condition when encountering a SOL, particularly in patients with a history of tuberculosis and spinal cord compression. In cases where a progressing neurological deficit is present, a combination of surgical intervention and anti‐tuberculous treatment should be considered as the optimal approach.https://doi.org/10.1002/ccr3.8131myelopathyspinal cordthoracic spinetuberculoma
spellingShingle Shyam Duvuru
Vivek Sanker
Syed Naureen
Gupta Prakash
Rajurkar Sanjana
Tirth Dave
Non‐osseous intradural tuberculoma of the thoracic spine with compressive myelopathy
Clinical Case Reports
myelopathy
spinal cord
thoracic spine
tuberculoma
title Non‐osseous intradural tuberculoma of the thoracic spine with compressive myelopathy
title_full Non‐osseous intradural tuberculoma of the thoracic spine with compressive myelopathy
title_fullStr Non‐osseous intradural tuberculoma of the thoracic spine with compressive myelopathy
title_full_unstemmed Non‐osseous intradural tuberculoma of the thoracic spine with compressive myelopathy
title_short Non‐osseous intradural tuberculoma of the thoracic spine with compressive myelopathy
title_sort non osseous intradural tuberculoma of the thoracic spine with compressive myelopathy
topic myelopathy
spinal cord
thoracic spine
tuberculoma
url https://doi.org/10.1002/ccr3.8131
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AT syednaureen nonosseousintraduraltuberculomaofthethoracicspinewithcompressivemyelopathy
AT guptaprakash nonosseousintraduraltuberculomaofthethoracicspinewithcompressivemyelopathy
AT rajurkarsanjana nonosseousintraduraltuberculomaofthethoracicspinewithcompressivemyelopathy
AT tirthdave nonosseousintraduraltuberculomaofthethoracicspinewithcompressivemyelopathy