Backgrounds: Tuberculoma is a granulomatous inflammatory process mimicking a neoplasm, both clinically and radiologically. Although those with an infratentorial origin are rare, this disease is still a diagnostic challenge using conventional workup. However, this disease should not be overlooked because it is essentially curable with proper diagnosis and therapy, usually, a Mycobacterium Tuberculosis (MTB) DNA test is performed. Methods: We retrospectively analyzed the clinical presentations, CSF results, and images of 11 MTB DNA positive and clinically cured cases of infratentorial tuberculoma. Results: Infratentorial tuberculoma usually deteriorated before antituberculosis treatment (ATT). Magnetic resonance imaging showed space-occupying lesions without specific features, 4 within the cerebellum and 7 within the brainstem. Evidence of systemic tuberculosis was found in only 1 case. Clinical manifestations included various combinations of focal signs and symptoms in the brain stem and cerebellum. Cerebrospinal fluid (CSF) findings were also nonspecific. The diagnoses of these cases were based on the positive tests of a nested polymerase chain reaction (N-PCR) assay. Trial therapy with antituberculous drugs resulted in clinical improvement, as documented by MRI in all patients. Conclusions: Infratentorial tuberculoma should be suspected in patients with infratentorial space-occupying lesions who live in geographic areas where tuberculosis is endemic.
Tuberculosis involvement of the central nervous system continues to represent a serious problem, particularly in developing countries [
Infratentorial tuberculoma is life-threatening, and clinical manifestations included various combinations of focal signs and symptoms of subacute onset, similar to those produced by other space-occupying lesions in the brain stem and cerebellum. There are isolated adults cases with brainstem and cerebellar tuberculomas reported worldwide in the last 10 years [5-9], wherein diagnosis was mainly at the time of surgery or at necropsy. The clinical diagnosis of this condition is difficult in practice, and a delay in the diagnosis of this curable disease contributes to significant neurologic sequelae. Conventional microbiology has limited utility, whereas efficient diagnosis by detection of Mycobacterium tuberculosis (MTB) DNA can provide a rapid diagnosis of CNS TB, possibly saving lives. We herein present eleven patients with infratentorial tuberculoma, diagnoses were established on positive test of MTB DNA. The purpose of this study is to stress that infratentorial tuberculoma may be misdiagnosed as a tumor.
This retrospective study was carried out at the Neurology Department of the First Affiliated Hospital of Sun Yat-sen University in southern China between 2005 and 2012. Our retrospective study consisted of 11 patients whose infratentorial space-occupying lesions were considered to be tumors, but were diagnosed as tuberculomas by MPB 64 targeted nested PCR. The inclusion criteria were: 1) space-occupying lesions in the brain stem and/or cerebellum on magnetic resonance imaging (MRI); 2) positive CSF MPB 64-targeted nested PCR in our lab; 3) good response to antituberculosis treatment.
The university ethics committee approved the study. Written informed consent was obtained from patients who agreed to participate in the study.
The age of the patients ranged from 17 to 75 years (mean 44.2 years). Three were female and eight patients were male (F/M ratio: 37.5%). The mean duration of neurological symptoms prior to admission was 51 days (14 days to 5 months). Double vision (4 cases), dizziness (4), unsteady gait (3), slurred speech (2), numbness and weakness on one side of the face (2), headache (2), hemiparesia (2), seizures (1), and vomiting (1). The evidence of tuberculosis in the lung was found in 1 patient. Fever occurred in just one patient. Two patients had a prior history of tuberculosis.
The CSF findings on admission were as follows: elevated opening pressure (>200 mm H2O) was present in 1 patient, CSF protein levels were increased (>0.45 g/L) in 6 patients, 4 patients had elevated CSF leukocyte counts, and 1 patient revealed a low CSF chloride level. The CSF/serum glucose ratio was normal for all patients. Overall, CSF was abnormal in 8 of 11 patients. CSF microscopy for AFB and CSF cultures were all negative. N-PCR for MTB DNA was positive in repeated tests for all these patients.
Magnetic resonance imaging (MRI) findings in all patients showed infratentorial space-occupying lesions: an iso-hipo intense in T1 sequence, a contrast-enhanced lesion in T1 sequence and hyper intense lesion in T2 sequence. Radiologically, those lesions were considered to be tumors. Solitary lesions were more prevalent. Among the lesions, four were located in the cerebellum (4/11) (
All patients experienced good response in the early course of ATT treatment. Paradoxical responses were seen in 2 patients. The No 1 patient experienced worsen
ing headaches with increased open CSF pressure during the second weeks of therapy. The headaches resolved in 12 days after mannitol treatment. The No. 11 patient was seen worsening dizziness with paradoxical enlargement of mass lesions, and it lasted 10 days. No alteration was made in the drug regimen in this patient.
All 11 patients were followed up regularly at the outpatient clinic. Side effects due to antituberculosis therapy developed in 3 patients. Mild gastrointestinal irritation was seen in 2 patients, and mild elevation in hepatic enzymes developed in 1. All these side effects were resolved quickly by active therapy and were able to continue the ATT treatment. The mean follow-up period was 4 years (range: 28 months to 6 years). Permanent neurological sequelae were observed in 1 patient. Two-year observations based on MRI imaging were completed for all patients. All infratentorial lesions were resolved after ATT treatment. No recurrent lesions were observed in the follow up time.
Case 1: A 59-year-old previously healthy male was referred to us with an occipital headache that he had for fifty days. He complained of gait disorder, throbbing headaches, and vomiting with inability to walk for 7 days. T1-weighted MR imaging revealed a low signal intensity area in the right cerebellar hemisphere and vermis (
Case 2: In June 2005, a 69-year-old Chinese man presented with diplopia and right face weakness and atrophy that lasted for 5 months, and right-sided weakness, hyperesthesia and slurred speech for that lasted for two weeks. He did not present with any cough, hemoptysis, fevers, chills, or weight loss. On neurological examination, he was alert and well oriented and did not have neck stiffness or other signs of meningeal irritation. He was found to have bilateral gaze-evoked nystagmus (with a rotatory component), and a right sixth nerve palsy with hyperreflexia and hyperesthesia on the left side of the body. There was decreased sensation over the right V 1 - 3 dermatomes, and the right corneal reflex and gag reflex were absent. There was a mild facial palsy and taste was impaired on the right side. A hemogram showed an elevated erythrocyte sedimentation rate of 16 mm/h and a normal white blood count. The Mantoux test was positive. A chest X-ray revealed right apical parenchymal infiltrates and consolidation. Sputum specimens stained negative for Acid Fast Bacilllus (AFB). FLAIR of brain MRI revealed extensive high signal lesions in the brain stem and right basal ganglia region (
The aim of this study was to increase the awareness of infratentorial tuberculoma, especially in patients with infratentorial space-occupying lesions who live in geographic areas where tuberculosis is endemic. Despite being preventable and curable, this disease is still a diagnostic challenge using conventional workup. A definitive diagnosis could not be made using routine CSF tests, and conventional MR because similar MR findings are more commonly found in infratentorial tumors.
Infratentorial tuberculoma poses a more risk to the patient life than supratentorial one, and are seldom reported. It may present with isolated mass lesion without evidence of systemic tuberculosis, mimicking tumors rather than the infectious process [
Unfortunately, diagnosis of CNS TB remains difficult. Although those reports demonstrated that neuroradiological findings might be helpful in the diagnosis of tuberculosis, However, MRI of the brain cannot distinguish between gliomas, lymphomas and tuberculomas with complete accuracy. Its diagnosis usually necessitates preferably, a stereotactic brain biopsy followed by, a histopathological examination. However, this invasive diagnostic procedure cannot identify etiologic agents in all patients [
Today, with the increasing incidence of tuberculosis, various studies have demonstrated that early diagnosis and treatment are essential since the patient outcome of CNS tuberculosis depends on the clinical stage and on the age of the patient [
In our case series, one patient presented with a “paradoxical” enlargement of a lesion during early treatment, and another patient presented with transient worsening due to intracranial pressure. This is presumably an immunologic response and usually a transient phenomenon [
There are methodological limitations to the current study. This is a small numbered retrospective study. The study did not evaluate the specificity and sensitivity of the nested-PCR test in the detection of MTB DNA in CSF. And therefore it is difficult to judge the true value of the test. However, It can be alert to us that tuberculoma may be misdiagnosed to be a tumor. For this reason, clinicians must always be aware of it and consider it in the differential diagnosis.
Our limited clinical experience of these disorders indicates that infratentorial tuberculomas should be suspected in patients with focal space-occupying lesions who live in geographic areas where tuberculosis is endemic. Diagnosis can be made by the combination of clinical presentation, imaging, MTB DNA test and response to treatment.
This work was supported in part by Guangdong Medical Research Foundation (Grant No. 2012B03180067).