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LETTER TO THE EDITOR |
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Year : 2014 | Volume
: 9
| Issue : 3 | Page : 295-297 |
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Concurrent intra-cranial tuberculoma and tuberculous abscesses: A rare combination
Satya Bhusan Senapati, Sudhansu Sekhar Mishra, Srikanta Das, Mani Charana Satpathy
Department of Neurosurgery, SCB Medical College and Hospital, Cuttack, Odisha, India
Date of Web Publication | 23-Dec-2014 |
Correspondence Address: Satya Bhusan Senapati Department of Neurosurgery, SCB Medical College and Hospital, Cuttack - 753 007, Odisha India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/1817-1745.147608
How to cite this article: Senapati SB, Mishra SS, Das S, Satpathy MC. Concurrent intra-cranial tuberculoma and tuberculous abscesses: A rare combination. J Pediatr Neurosci 2014;9:295-7 |
Dear Sir,
Although tuberculosis of the central nervous system is well-known, the incidence of tuberculous brain abscesses (TBAs) is rare, more so its association with concurrent intra-cranial tuberculoma.
A 6-year-old immunocompetent child with contact history of tuberculosis, presented to us in unconscious state with complains of intermittent fever, night sweats, headache, left sided weakness and progressive visual impairment in both eyes for last 4 months. Two days back he had several episodes of left sided complex partial seizure, following which he became unconscious. Neurological evaluation showed a decorticating child with secondary optic atrophy. Plain computed tomography (CT) scan revealed right fronto-parietal multiple cystic lesions with a separate solid component [Figure 1]a. There was perilesional edema, midline shift and herniation. An urgent craniotomy was done, straw colored cystic fluid aspirated followed by removal of multiple cysts one after another. All the cysts were well encapsulated having clear cyst-parenchyma interface. Solid component was firm, yellowish white, avascular and well demarcated. It was removed in piecemeal totally [Figure 2]. Postoperative CT scan confirmed total removal of the lesion with relief of hydrocephalous [Figure 1]b. Histopathological examination of solid component showed a granulomatous inflammation with central caseous necrosis, containing epithelioid cells and multinucleated giant (Langhans) cells, whereas the histopathological examination of cyst wall showed chronic inflammatory cells without granuloma formation [Figure 3]. Ziehl Neelsen staining of pus revealed the acid fast bacilli and pus cells [Figure 4]. Patient's screening for any systemic source of tuberculosis was negative. Postoperatively child improved clinically. He was discharged with anti-tubercular regimen (Category II regimen of DOTS) started and continued for 15 months. At 2 years follow-up, the patient was doing well. | Figure 1: (a) Plain computed tomography (CT) scan showing right fronto-parietal multiple cystic lesions (red arrow) with a separate solid component (blue arrow), perilesional edema, midline shift and herniation. (b) Postoperative CT scan showing complete removal of lesion with relief of hydrocephalous
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 | Figure 2: Well encapsulated excised cyst wall, solid granulomatous mass and pus in syringe
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 | Figure 3: Histopathological examination of abscesses wall showed chronic inflammatory cells without granuloma formation
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 | Figure 4: The Ziehl Neelsen stain of pus showing many acid-fast bacilli and pus cells
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After Whitener [1] reviewed the world literature, isolated cases of TBAs have been reported. [2],[3],[4] TBA, by definition, is an abscess containing tubercle bacilli in the pus but the lack of granulomas in the wall. All these criteria were met during diagnosis of TBA in the present case report.
The diagnosis of tuberculous brain abscess is, usually, suspected in immunocompromised patients with or without human immunodeficiency virus infection or in an immunocompetent patient from an endemic region with a pulmonary focus of infection. This pulmonary focus of infection is, usually, present in only 30% of cases. [5] In the absence of an extracranial focus of infection, it might be very difficult to suspect tuberculous brain abscess on the basis of clinical and imaging features as they resemble pyogenic brain abscesses. In vivo proton magnetic resonance (MR) spectroscopy and magnetization transfer MR imaging may differentiate tuberculous from pyogenic abscesses and influence management. [6] Newer techniques like polymerase chain reaction may provide a useful tool for diagnosis of tuberculosis from paucibacillary specimens like pus in which conventional methods may show low sensitivity. [7] Recently in vitro proton MR spectroscopy was evaluated for the diagnosis of TBA. Absence of multiplet of amino acids-lipids at 0.9 ppm seems to be a hallmark of TBA. [8]
References | |  |
1. | Whitener DR. Tuberculous brain abscess. Report of a case and review of the literature. Arch Neurol 1978;35:148-55. |
2. | Ramesh VG, Sundar KS. Concomitant tuberculous and pyogenic cerbellar abscess in a patient with pulmonary tuberculosis. Neurol India 2008;56:91-2.  [ PUBMED] |
3. | Gazzaz M, Bouyaakoub FA, Elkhamlichi A. Tuberculous cerebellar abscess. Acta Neurol Belg 2000;100:46-7. |
4. | Farrar DJ, Flanigan TP, Gordon NM, Gold RL, Rich JD. Tuberculous brain abscess in a patient with HIV infection: Case report and review. Am J Med 1997;102:297-301. |
5. | Barnes PF, Bloch AB, Davidson PT, Snider DE Jr. Tuberculosis in patients with human immunodeficiency virus infection. N Engl J Med 1991;324:1644-50. |
6. | Gupta RK, Vatsal DK, Husain N, Chawla S, Prasad KN, Roy R, et al. Differentiation of tuberculous from pyogenic brain abscesses with in vivo proton MR spectroscopy and magnetization transfer MR imaging. AJNR Am J Neuroradiol 2001;22:1503-9. |
7. | Kaushik K, Karade S, Kumar S, Kapila K. Tuberculous brain abscess in a patient with HIV infection. Indian J Tuberc 2007;54:196-8. |
8. | Menon S, Bharadwaj R, Chowdhary A, Kaundinya D, Palande D. Tuberculous brain abscesses: Case series and review of literature. J Neurosci Rural Pract 2011;2:153-7.  [ PUBMED] |
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
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