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Tuberculous subdural empyema mimicking chronic subdural hematoma
*Corresponding author: Krishnan Nagarajan, Department of Radio-Diagnosis, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India. lknagarajan1@gmail.com
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Received: ,
Accepted: ,
How to cite this article: Soundappan V, Nagarajan K, Sunitha VC. Tuberculous subdural empyema mimicking chronic subdural hematoma. J Neurosci Rural Pract 2023;14:554-5.
Dear Editor,
We read the interesting case series by Rengarajan et al.[1] and share our comments on the same. Calvarial osteomyelitis is uncommon and usually presents with scalp subgaleal swelling, lytic skull lesion, and occasionally extra- or subdural collections.[2-4] The clinical presentations include scalp swelling similar to the cases, discharging sinus, seizures, or even signs of meningitis. The management is surgical debridement with anti-tuberculous chemotherapy. If the skull bony erosions are minimal without any empyema causing mass effect, only anti-tuberculous therapy may be tried after cytology from the scalp collection.[5]
Forty-nine-year-old male presented with the right-sided scalp swelling and headache for the past 2 months. There was no history of injury. He had low-grade fever twice in the past 2 months. On examination, there was “boggy” scalp swelling in the right frontoparietal region. There was mild tenderness, but no warmth was noted. The swelling was not pulsatile or compressible. Plain computed tomography (CT) scan was done which showed large mixed-density right frontoparietal extradural and subdural collections with loculations and posterior dependent layering giving the appearance of acute-on-chronic subdural hematoma (SDH). There was also a large right frontoparietal scalp subgaleal collection [Figure 1]. The underlying frontoparietal one around the coronal suture showed patchy rarefaction with diploic thinning suggestive of bone erosion. With the above findings, possibility of osteomyelitis of right frontal calvarium was considered with subdural empyema and subgaleal “cold” abscess formation. The patient was taken up for decompression and en bloc excision of infected bone was done with drainage of intra- and extracranial collections.
In the current case, there were both extra-and subdural collections with mass effect, and hence, decompression and confirmation of tuberculous etiology was done. The initial diagnosis in our middle-aged patient was chronic SDH as it can present without history of trauma or occasionally trivial trauma. The possibility of infective origin like tuberculous etiology should be considered in unexplained scalp swelling that is unaccompanied by a history of trauma. Further, the bone erosion may be missed unless bone window settings are used to see the underlying bone in routine brain CT evaluation as CT brain window may not show the erosions. The combination of extracranial scalp subgaleal and extra-or subdural collections should give rise to the possibility of underlying skull bone osteomyelitis and bone window should be scrutinized for erosions and changes. This is more so particularly when there is no history of trauma in such a patient with both extra- and intracranial collections.
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References
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