INTRODUCTION
Central nervous system (CNS) tuberculosis (TB) is a severely debilitating and potentially life-threatening illness.1 Although tubercular meningitis has been extensively studied, there is limited research on the management and outcomes of tubercular mass lesions, particularly large tuberculous mass lesions (LTML). These lesions often cause significant mass effects and present unique treatment challenges. The optimal management approach for LTML remains controversial, with some clinicians advocating for upfront surgical intervention, whereas others prefer conservative management with antitubercular therapy and steroids.2 Our study aims to bridge this knowledge gap.
MATERIALS AND METHODS
Study design.
We conducted a single-center, retrospective observational study of patients with CNS LTML from January 2010 to February 2023 at a 3,800-bed quaternary care center in South India.
Participants.
Adult patients (aged ≥15 years) with intracranial mass lesions sized ≥3 cm and radiological evidence suggestive of tuberculoma (brain magnetic resonance imaging: well-marginated enhancing lesions with or without meningitis; brain computed tomography (CT): peripherally enhancing lesion with a low attenuation center surrounded by vasogenic edema) were included in the study. Patients with confirmed alternative etiologies were excluded. All patients received antitubercular therapy (ATT), with or without steroids and surgery, as treatment.
Data collection and follow-up.
We documented patients’ demographics, neurological signs and symptoms, treatment, and both baseline and follow-up imaging. We recorded the clinical and neurological outcomes of the patients during the baseline and follow-up visits at 6 months using a modified Rankin score (mRS). Telephone calls were made when follow-up data were incomplete.
Primary outcome.
The primary outcome was independence in activities of daily life (scores of 0, 1, and 2) at 6 months, as assessed by the mRS, compared with baseline, or the resolution of all symptoms or signs if the patient was already independent at baseline.
STATISTICAL ANALYSES
The descriptive statistics were analyzed using frequency and percentages for categorical variables, as well as mean and SD and median and interquartile range (IQR), for continuous variables. Associations between good outcomes and clinical predictors were assessed using the appropriate χ2 or Fisher’s exact test. Continuous variables were compared using the independent t-test or Mann–Whitney U test, depending on the distribution. The Wilcoxon signed rank test was used to assess the median difference between absolute baseline and follow-up mRS scores. Factors with a P <0.05 were included in the multivariate analysis. The independent effects of factors associated with good outcomes were evaluated using multiple logistic regression. All analyses were performed using the statistical software IBM SPSS Statistics (Version 23; IBM Corp., Armonk, NY).
RESULTS
We screened patients using our picture archiving and communication system for magnetic resonance/CT imaging, identifying any CNS mass lesions from 2010. Of the total 1,641 patients with ring-enhancing lesions in the brain, 169 had lesions measuring greater than or equal to 3 cm with various etiologies, including tuberculomas, gliomas, neurocysticercosis, and pyogenic abscesses. Among these, 46 patients with tuberculous LTML were included in the study.
The mean age of the patients was 27.6 years (SD ± 12), and the majority were female (25/46; 54.3%). None of the patients had concomitant HIV infection. Twenty-two (48%) patients had microbiologically confirmed TB, of which most cases were rifampicin-susceptible TB (44/46; 95.7%), and 52% had a biopsy showing granulomatous inflammation. Two patients had multidrug-resistant TB. Sixteen patients (34.8%) had probable tuberculomas based on clinical and radiological imaging findings alone. Almost half (24/46; 52.2%) had disseminated TB, and one-quarter (11/44; 25%) had chest X-rays suggestive of TB (as detailed in Supplemental Table 1). The median duration of antituberculous therapy (ATT) was 18 months (IQR 15–24), and the median duration of follow-up was 20 months (IQR 15.5–40). Two patients were reported dead at follow-up.
The index clinical presentations were focal neurological deficit (24/46, 52.2%), seizure (22/46, 47.8%), and symptoms of raised intra cranial pressure (ICP) (11/46, 23.9%). The median duration of illness at presentation was 4 months (IQR 2–9). On imaging, 30 of 46 (65.2%) patients had a midline shift, and 6 of 46 (13%) had lesions measuring greater than 5 cm. Almost one-third of patients (14/46 [30.4%]) had tuberculomas and tuberculous meningitis. A third of patients (14/46 [30.4%]) had lesions in the frontal lobe, followed by the cerebellar (9/46 [19.6%]), parietal (8/46 [17.4%]), and temporal (6/46 [13%]) regions; 6 of 46 (13%) patients had extensive lesions involving multiple lobes, and 3 of 46 (6.5%) had thalamic lesions.
The primary outcome was observed in 33 of 46 patients (71.7%). The median absolute mRS at baseline in the study was 2 (1–3), and at the 6-month follow-up, it was 1 (0–2). In Supplemental Table 2, only focal neurological deficits (RR 0.2 [95% CI 0.05–0.95]; P = 0.043) showed a significant risk for poor outcomes in univariate analysis. However, when analyzed in a multivariate model, none were found to be statistically significant.
Radiologically, the majority of patients (27/41 [65.8%]) showed significant improvement, 10 of 41 (24.3%) showed moderate improvement, and 4 of 41 (9.7%) showed no improvement. Additionally, 5 of 46 (10.8%) did not undergo follow-up imaging (Supplemental Figure 1). All patients received one of the following four possible therapy modalities: 13 of 46 (28.3%) received ATT alone, 16 of 46 (34.8%) received ATT and steroids, 8 of 46 (17.4%) received ATT with tuberculoma excision, and 9 of 46 (19.6%) received ATT, steroids, and tuberculoma excision. A significant number of patients (17/46 [37%]) underwent surgery. Better outcomes were not noted with surgery (87.5%) or the addition of steroids (62.5%) to antimycobacterial therapy (P = 0.637). In the subgroup analysis of 34 of 46 (73.9%) patients with signs and symptoms of raised ICP with midline shift, no difference in successful outcomes was observed between patients who underwent surgery and those managed conservatively with only medical therapy (10/13 [76.9%]) versus 3/13 [23.1%] and 15/21 [71.4%] versus 6/21 [28.6%]; P = 1.00).
DISCUSSION
To the best of our knowledge, this study represents the first comprehensive evaluation of patients’ presentations, treatment strategies, and outcomes associated with LTML. Despite the large lesions and associated edema, most patients had good outcomes at 6 months. Our outcomes are superior to those of many CNS tuberculoma cohorts across the globe and similar to other reports from this region.3–6 Low rates of HIV co-infection, drug-resistant TB, and secular trends in management strategies over the years may explain these findings.
An important question in the management of LTML concerns the role of steroids and surgery as adjuncts to antitubercular therapy. Although specific data concerning LTML are not available, some guidelines endorse the use of steroids in the management of CNS TB beyond TB meningitis.7 However, a clinical trial or well-matched prospective study has yet to evaluate this question.
Steroid use remains prevalent in tuberculoma cohorts.3,4,6 Nevertheless, steroids may impair the penetration of antitubercular agents, particularly isoniazid, into the CNS, and tuberculomas often develop in TB meningitis during treatment despite corticosteroid therapy.8,9 In our study, steroid administration was not associated with improved outcomes. Furthermore, steroids do not appear to influence the development or resolution of CNS mass lesions, especially when the size exceeds 3 cm.3
A small subset of patients with LTML who experience severe paradoxical worsening, life-threatening mass effects, or the involvement of specific locations, such as the posterior fossa, may benefit from steroids and surgery.10,11 However, the routine use of steroids and surgical intervention in LTML may not be warranted and requires further investigation.
Our study has several limitations. The retrospective, observational nature and limited sample size present challenges in evaluating therapeutic interventions. Additionally, not all patients had microbiologically confirmed TB. In conclusion, our preliminary data indicate that the majority of patients with LTML demonstrate favorable neurological outcomes at 6 months, and the routine use of high-dose steroids and surgery necessitates further study.
Supplemental Materials
ACKNOWLEDGMENT
The American Society of Tropical Medicine and Hygiene (ASTMH) assisted with publication expenses.
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