Medullary tuberculosis mimicking a multiple schwannoma

• Tuberculosis is endemic in Africa, especially in sub-Saharan Africa. • Medullary tuberculosis is unique and can sometimes mimic another disease. • Diagnosis is not easy. • The management is medicosurgical. • The evolution is favorable so quickly managed followed by anti-tuberculosis treatment over 1 year to 18 months. • No clear protocol for its management yet. Despite progress in the management of Tuberculosis (TB), it remains a major public health problem. Intramedullary tuberculosis is rare, and the rarity of this disease in the medullary cone makes preoperative diagnosis difficult. We report a case of intramedullary tuberculosis assimilated to a multiple schwannoma. A 14-year-old patient presented with a 7-month history of decreased hearing associated with micturition problems ranging from overflow voiding to acute urine retention 2 weeks ago. Clinical examination revealed right-sided hypoacusis and terminal cone syndrome. On paraclinical examination, audiometry showed conductive hearing loss on the right and a slight transmission loss on the left. A CT scan of the hip did not reveal any abnormality in the urinary tract. Thoracolumbar MRI showed a diffuse intramedullary lesion extending between T11 and L1, suggesting a low-grade glial lesion, particularly an astrocytoma or ependymoma. Given the auditory symptoms, the hypothesis of a multiple neuroma with cerebral and intramedullary localization was raised and a cerebral CT scan performed for this purpose came back normal. Tumour resection revealed a heterogeneous whitish process with a fleshy and soft necrotic portion. The pathological examination concluded that the tumor was tuberculous. The PCR came back negative and the patient was put on anti-tuberculosis treatment and corticosteroid therapy for 30 days. Progression was favorable, with progressive motor recovery from day 6 and complete recovery at day 60. Hearing loss persisted and was managed by ENT specialists. Intramedullary tuberculosis remains a reality. The insidious clinical picture and the atypical imaging appearance are factors in misdiagnosis. An effective meta -analysis would be timely to clarify the diagnostic presentation and allow agreement on the role of surgery in the face of chemotherapeutic measures.

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Publication Details

Journal
Interdisciplinary Neurosurgery
Published
2025-05-10
DOI
https://doi.org/10.1016/j.inat.2025.102046
Primary Topic
Infectious Diseases and Tuberculosis
Type
article
Field-Weighted Citation Impact
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article

Medullary tuberculosis mimicking a multiple schwannoma

Mèhomè Wilfried Dossou, Nicaise Kpègnon Agada, Laté Dzidoula Lawson, Konan Médard Kakou et al.
Interdisciplinary Neurosurgery
Infectious Diseases and Tuberculosis
article

Medullary tuberculosis mimicking a multiple schwannoma

Mèhomè Wilfried Dossou, Nicaise Kpègnon Agada, Laté Dzidoula Lawson, Konan Médard Kakou, Ibrahim Assoumane, Wilfried Innocent Munkado Meuga
article en

Abstract

• Tuberculosis is endemic in Africa, especially in sub-Saharan Africa. • Medullary tuberculosis is unique and can sometimes mimic another disease. • Diagnosis is not easy. • The management is medicosurgical. • The evolution is favorable so quickly managed followed by anti-tuberculosis treatment over 1 year to 18 months. • No clear protocol for its management yet. Despite progress in the management of Tuberculosis (TB), it remains a major public health problem. Intramedullary tuberculosis is rare, and the rarity of this disease in the medullary cone makes preoperative diagnosis difficult. We report a case of intramedullary tuberculosis assimilated to a multiple schwannoma. A 14-year-old patient presented with a 7-month history of decreased hearing associated with micturition problems ranging from overflow voiding to acute urine retention 2 weeks ago. Clinical examination revealed right-sided hypoacusis and terminal cone syndrome. On paraclinical examination, audiometry showed conductive hearing loss on the right and a slight transmission loss on the left. A CT scan of the hip did not reveal any abnormality in the urinary tract. Thoracolumbar MRI showed a diffuse intramedullary lesion extending between T11 and L1, suggesting a low-grade glial lesion, particularly an astrocytoma or ependymoma. Given the auditory symptoms, the hypothesis of a multiple neuroma with cerebral and intramedullary localization was raised and a cerebral CT scan performed for this purpose came back normal. Tumour resection revealed a heterogeneous whitish process with a fleshy and soft necrotic portion. The pathological examination concluded that the tumor was tuberculous. The PCR came back negative and the patient was put on anti-tuberculosis treatment and corticosteroid therapy for 30 days. Progression was favorable, with progressive motor recovery from day 6 and complete recovery at day 60. Hearing loss persisted and was managed by ENT specialists. Intramedullary tuberculosis remains a reality. The insidious clinical picture and the atypical imaging appearance are factors in misdiagnosis. An effective meta -analysis would be timely to clarify the diagnostic presentation and allow agreement on the role of surgery in the face of chemotherapeutic measures.

Interdisciplinary NeurosurgeryVol. 40
Université Abdou Moumouni (NE), Futures Group (United States) (US), National Hospital Niamey (NE), Université Félix Houphouët-Boigny (CI)
Zero hunger
Openalex Percentile: Top 82%
Infectious Diseases and Tuberculosis
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