Case Report

Confirmed Neuromeningeal Tuberculosis in Patients Living with HIV

Badi Hanane*, El Fane Mouna, Oulad Lahsen Ahd, Sodqi Mustapha, Marih Latifa, Bensghir Rajaa, Chakib Abdelfettah and Marhoum El Filali Kamal

Department of infectious diseases, Ibn Rochd University Hospital, Morocco

Submission: January 25, 2019; Published: March 12, 2019

*Corresponding author: Badi Hanane, Department of infectious diseases, Ibn Rochd University Hospital, Morocco

How to cite this article: Badi H, E Fane M, Oulad L A, Sodqi M, Marih L, et al. Confirmed Neuromeningeal Tuberculosis in Patients Living with HIV .Open Access J Neurol Neurosurg. 2019; 9(5): 555775. DOI: 10.19080/OAJNN.2019.09.555775.

Abstract

Introduction: Neuromeningeal tuberculosis remains a public health issue in low- and middle-income countries. The huge clinical and radiologic polymorphism is frequently responsible of a delay in diagnosis and then in patient’s care. The aim of this study is to describe the clinical, paraclinical and the evolutive course of neuromeningeal tuberculosis in patients living with HIV.

Patients and methods: It’s a retrospective study including patients living with HIV who had a confirmed neuromeningeal tuberculosis and been cared for in the infectious diseases department of Ibn Rochd University Hospital of Casablanca between January 2012 and December 2017. The data were collected from computerized medical files on Nadis software.

Results: We gathered thirty-two patient’s files, among whom seventeen females with a mean age of 36±39 years old. The median of CD4 levels was 186 cells/mm3. The mean time line between the beginning of the symptoms and the seek of care was thirty-three days (6-90 days). The neuromeningeal tuberculosis revealed HIV in 20 cases (62.5%). The main clinical presentations were the meningitis syndrome in 22 cases and unconsciousness in 7 cases. The head scan realized on all patients was abnormal in 69% of the cases showing tuberculoma in six cases, hydrocephalus in seven cases and a hypodensities in nine cases. The cerebro-Spinal Fluid (CSF) was clear in 29 cases with lymphocytosis, high levels of proteins and low glycorrachia levels in respectively 75%, 90%, and 75% of the cases. Ziehl-Neelsen staining was negative in all cases and Lowenstein culture positive in 78% of the cases. The TB-PCR on CSF was positive on all fifteen cases that benefited from it. Eighteen patients had other localizations, fifteen of which are pulmonary tuberculosis and ten others are lymph node tuberculosis. The mortality rate was 53%.

Conclusion: Neuromeningeal tuberculosis has an extremely heterogeneous clinical and radiologic presentation among HIV infected patients. The prognosis depends on the immune status of the patient and the time line between the diagnosis and the instauration of treatment.

Keywords: Confirmed neuromeningeal tuberculosis; Cerebrospinal fluid; Tuberculoma; HIV infection

Abbrevations: ART: Antiretroviral Therapy, CSF: Cerebrospinal Fluid’s, IRIS: Inflammatory Syndrome, UHC: University Hospital Center, ZN: Ziehl-Neelsen, PCR: Polymerase Chain Reaction, AFB: Acid-Fast Bacilli, NAA: Nucleic and Amplification

Introduction

Tuberculosis (TB) remains a major public health problem in Morocco and represents the most frequent AIDS-defining opportunistic infection [1]. The annual incidence of TB in Morocco was estimated at 83/100 000 people per year in adult population and the prevalence of HIV infection among TB patients is 1.7% [2]. HIV intensely increases the risk of Tuberculous Meningitis (TBM) because there is a higher susceptibility to reactivating and disseminating TB in these patients [3,4]. TBM is one of the most severe and lethal complications of TB [5]. TBM is caused by the hematogenous spread of the pulmonary bacilli or from the rupture of sub-ependymal tubercule into the subarachnoid space [6,7]. However, the mechanism by which the bacilli invade the blood-brain barrier and the exact trigger of discharge into the subarachnoid space is not fully understood yet [6]. TBM diagnosis and treatment are complicated due to the variable Cerebrospinal Fluid’s formula presentation (CSF), the drug interactions and the decision making of the proper timing of Antiretroviral Therapy (ART) initiation after starting the patient on TBM treatment with an awareness of the possibility of an occurrence of an immune reconstitution Inflammatory Syndrome (IRIS) [3]. IRIS develops in 9 to 47% HIV patients who are diagnosed with TBM and who started ART; it is associated with a mortality rate of 13 to 75% [8]. TBM in patients living with HIV have an increased risk of poor clinical outcomes with mortality rates as high as 67% against 25% of HIV negative patients [7]. In Morocco, the studies are scarce even with the gravity of HIV and TB infections situation. Furthermore, although all patients have a free access to ARV and TB medications, the majority of HIV-infected patients with TBM still present with severe immunosuppression. This study was designed to outline the characteristics of TBM in HIV infected patients in Morocco.

Materials and Methods

This was a retrospective study of TBM in HIV infected patients at the University Hospital Center (UHC) of Casablanca, conducted between January 2012 and December 2017. The diagnosis was based on combining the clinical symptoms, CSF analysis and radiological features and confirmed by culture or TB-PCR on CSF. All patients benefited from a macroscopic examination, a protein and glucose quantification, a cell count, a Ziehl-Neelsen (ZN) staining and Mycobacterium tuberculosis culture on Lowenstein-Jensen medium on CSF. Some patients had also TB Polymerase Chain Reaction (PCR) tests (real time PCR, 2720 thermal technology, applied biosystem by life technology, USA). Brain CT was performed in all cases to exclude mass effect prior to lumbar puncture and brain MRI when indicated to highlight tuberculoma. Tuberculomas were identified as a low or high-density rounds or lobulated masses with irregular borders showing ring enhancement after contrast injection. Chest X-ray and sputum samples were collected to look for pulmonary TB. Further analysis were indicated according to symptoms. CSF finding consistent with TBM include high protein, low glucose and a high mononuclear to polynuclear leucocyte ratio. Identification of M. tuberculosis thanks to culture and molecular analysis. Patients were treated with standardized TB treatment; including isoniazid, rifampicin, pyrazinamide, and ethambutol for two months, followed by rifampicin and isoniazid for at least seven months. Total duration varied from nine to twelve months. ART was advised for all patients. The first line of treatment was tenofovir, emtricitabine, efavirenz or nevirapine. Data were collected from computerized medical files on Nadis software and analyzed using Excel support.

Results

All patients underwent brain CT though 19% of them had brain MRI with gadolinium, the majority of which (n=22, 68.7%) was abnormal: a hypodensity was seen in 9 (28%) cases, 7 (22%) demonstrated hydrocephalus and tuberculoma was found in 6 (18.7%) cases. (Figures 1&2). CSF examinations are summarized in Table 1 75% of cases showed a lymphocytic pleocytosis. The median protein level was 0,83mg/dL (IQR: 0.2- 3.09), median glucose level was 0,4 mg/dL (IQR: 0.18-1.38) and median white cell count (WCC) was 108 cells/ml (IQR: 0-700). A protein level was more than 0.4 mg/dL in 29 (90 %), a glucose concentration was less or equal to 0.45 mg/dL in 24 (75%) cases. No Acid-Fast Bacilli (AFB) smears were positive. Mycobacterium tuberculosis was cultured from 25/32 CSF samples (78 %). PCR was positive in fifteen cases (n: 15/32, 47%); No TB was of a multidrug resistant. Eighteen (56%) patients had extrameningeal TB. Chest radiography was consistent with TB in 15 (83%) cases, the most frequent pulmonary lesions identified were infiltrates (57%) and cavities (26%). Four (22%) patients presented with miliary TB. Ten (55.5%) patients had lymph node tuberculosis; four had hematopoietic tuberculosis and two scrotal localization. The median CD4 count was 186 cells/μL (IQR = 39-237). The majority of patients (78%) had CD4 count less than 200 cell/mm3. HIV diagnosis was concomitant to TB diagnosis in 62.5% of cases. Only four patients (12.5%) were receiving ART at the time of hospital admission. TB treatment was initiated immediately after clinical suspicion for a period of 9 to 12 months. Adjunction of steroid therapy was initiated in 69% cases at a dose of 1.5 mg/kg/day during the first month and gradually reduced during the second month. Nine (28%) patients developed reversible side effects: five with Isoniazid and four with Rifampicin. Four patients (12.5%) needed a ventriculo-peritoneal shunt for hydrocephalus. Three (9.3%) patients developed IRIS with a median of time onset of three to six months. Thirteen (41%) patients well recovered after TB treatment on 12 months follow up. Two patients (6 %) had a residual disability. Inpatient mortality was 53% in average of ten days after admission. Details are shown on Table 2.

Discussion

The increased incidence of HIV infection has led to the resurgence of TB in Morocco. Neurological TB occurs in 5 to 8 % in HIV infected patients; five times more frequent than in HIV negative patients [6,9]. TBM accounts for approximately 1% of all cases of TB [5]. This study founded that the prevalence of confirmed TBM in HIV infected patient at the UHC of Casablanca was 1,14%. This result was lower than that in studies conducted in Cameroon (8%) and India (7%) [3]. TBM occurs most often in persons over 45 years, frequently appearing as a reactivation of a latent infection [10]. In our study, the most affected age group was between 21-45 years in 81 % of the cases. This could be explained by the young age of our population and the high incidence of TB in our country. A slight female dominance was observed, this could be explained by the feminization of HIV in Morocco. The prevalence of CNS-TB infections in females have been described in other studies from developed countries and suggest a gender related difference in the pathogenesis of TB [11].

The typical clinical presentation of meningitis is rarely found, the clinical spectrum is wide, and the onset of symptoms may be insidious or abrupt [7]. Usually, HIV infection does not modify the presentation of TBM [12], however, during HIV infection, the diagnosis of TBM is tricky due to the various diagnostic possibilities of opportunistic intracranial infections and malignancies [3]. Typical meningeal stiffness was observed in 69% of our patients and the most frequent clinical symptoms were headache (87%) and fever (46%), similar to those in other studies [6,7,13-15]. This difference could be explained by lower CD4 count of our patients and patients more severely immune depresses will present unusually [16].

However, our study was distinguished by the frequency of unconsciousness noted in 22% of cases. More so, TBM have an insidious onset with variable duration of symptoms from a few days to several months [7]. The gradual onset of symptoms before hospitalization noted in 84% of cases in our study is the same in Luma and al study [7]. Atypical CSF result are more common in HIV patients, including lower CSF protein, higher glucose levels, lower CSF WCC and even completely normal CSF finding have been reported in 25% to 33% of HIV patients with TBM [16-22]. The absence of CSF pleocytosis occur generally in patients with lymphopenia (CD4 T cell counts <50 cells/ MI), which may explain the low lymphocytes count in the CSF [7, 21]. We found that the median WCC was much higher than in other studies [7,23]. The identification of Mycobacterium tuberculosis in CSF is the gold standard for diagnosis and for drug-susceptibility testing. Though, CSF MT culture is slow and insufficiently sensitive (roughly 60-70%) [3,6,24,25]. This fact is matched in our study where confirmed diagnosis by culture was obtained in 78% of patients. Thus, CSF microscopy analysis with Ziehl-Neelson staining for AFB (acid fast bacilli) is the test used most often worldwide for TB diagnosis but has poor sensitivity (10-20%) in TBM and cannot be relied upon to rule out TBM [3,13, 26, 27]. However, the sensitivity can be improved by increasing the CSF sample volume to 6 ml and shortening the time for examination of the slide [6,7]. In this study, in all cases, the CSF microscopy analysis was negative. Other study had same results [7]. Nucleic and Amplification (NAA) tests on CSF have better sensitivity and specificity compared to microscopy and culture and it can speed up the diagnosis of tuberculosis from several weeks to 2 days [3,9]. In our study, PCR improved the diagnostic performance by confirming the diagnosis in fifteen smears.

For radiographic assessment of TBM, MRI is superior in detecting typical findings of TBM. However, in our unit, CT scan is a common practice in CNS disease investigation. The typical finding of TBM including brainstem involvement, leptomeningeal enhancement, vascular and cranial nerve involvement [28-30]. However, these radiographic finding are not specific to TBM and may not be sufficient to exclude other CNS co-infections [3]. An increased rate of tuberculoma in patients co-infected HIV-TB versus HIV negative patients is reported [3,13]. In our study, tuberculoma was seen in 18.7% of the cases, this finding is similar to that seen in one study from India (21%) [31], and lower than what was reported in other study (45%) [6]. Infarctions and communicating hydrocephalus are also reported in TBM [32].

They were present in only 10% of the cases [13]. They were seen on CT scans in 12% and 28% respectively of adults with TBM in other study [33,34]. The presence of extra-meningeal TB should be searched for any case of TBM using microscopy and mycobacterial culture of appropriate extra-meningeal specimens including sputum [3]. Chest x-ray finding were abnormal in 47% of our cases and four patients becoming culture positive. This shows the importance of not trusting chest-x ray and sputum to support the diagnosis of TBM [9,13]. HIV infection is recognized as the most common risk factor associated with TBM and TBM may be the initial presentation of HIV infection, as was perceived in 62.5% of our patients [35,36]. Consequently, HIV status should be defined if TBM is diagnosed [9]. Furthermore, sever immune suppression increases the odds of having TBM [36,37]. Leeds and al were reported that HIV infected patients with extrapulmonary TB and CD4 less than 100 were more likely to have TBM [4]. Other studies had also found that declining CD4 lymphocytes count can be associated with increasingly severe form of TB including TBM, but this remained understudied [36,38]. This is consistent with the results we got when most of patients had severe immune suppression. Previous studies reported also results of severe immune suppression with median CD4 count reaching sixteen to fourteen [7,23,39]. This finding contrasts a previous study conducted by Kingkaew and al, which found that 71,8% of HIV infected patients with TBM had CD4 lymphocyte counts < 100 [40].

TB treatment should be started on once TBM is suspected because of the high case fatality [3,7]. In Morocco, the TBM treatment regimens are standardized and comply with international recommendations including those of the WHO and international Union against Tuberculosis and Lung Disease [41]. All the French and American scientific societies recommend the use of steroids in addition to TB treatment, although the results of literature are not all consistent [42-44]. In a study of 270 patients, the use of corticosteroids does not find a significant improvement in survival adult patients with TBM [45]. Another study including 545 patients showed that the adjunction of dexamethasone to the anti-TB regimen reduced mortality but did not prevent disability in survivors [46]. TBM is the most lethal form of TB especially in HIV infected patients severely immune depressed [47]. Its mortality rates are considerably increased due to HIV infection, with 9 months survival rates less than 40% in HIV infected patients, compared with more than 70% in HIV negative patients [3]. 53% of our patients died, this case fatality is lower than that found in another study (79%) [23]. Higher mortality rates have been described in another study conducted in Cameroon. Studies from Brazil and China reported mortality rates of 29% [40].

In HIV infected patients, a lower CD4 cell counts [3,23], asymmetric neurological exam and altered consciousness on admission, were found to be a factor associated with a poor prognosis [47]. Previous study found also an association between immune suppression, neurological deterioration at admission and poor prognosis in HIV infected TBM patients [6,48,49]. Some studies reported other factors associated with death including disease progression of more than 14 days, drug resistance TB and low serum sodium concentration [23,49]. EL Sahly and al found that older patients were more likely to die within 180 days of diagnosis than younger patients [50]. TBIRIS is a severe complication, in HIV infected patients receiving TB treatment. It occurs usually approximately 2 weeks after the introduction of ART (30%) [6]. TB-IRIS is characterized by high CSF neutrophil count and Mycobacterium tuberculosis culture positivity [49].

Cases of expanding tuberculomas and abscesses have been described in paradoxical TBM-IRIS [3]. There is no mutual agreement on treatment in terms of using steroids and the prolongation of its duration [3]. IRIS has been reported in twenty to forty percent of patients receiving TB therapy for TBM in other studies conducted in South Africa [49,51]. There were limitations to our study. Its retrospective nature, the small sample size and the study concerned only patients with confirmed TBM in one referral hospital which does not capture the global picture of the problematic of TBM among HIV-infected patients in Morocco. However, the study conclude to information that can help clinicians in diagnosis and management of TBM in HIV patients especially in a setting with limited resources.

Conclusion

What to conclude from our study is that TBM may be the initial presentation of HIV infection. Clinical presentation and lab exams are often atypical. Physicians should do a LP in the presence of any warning sign of meningitis. We have also found that TBM has a high rate of mortality in PLWH and advanced HIV stage and the presence of neurological symptoms at admission are correlated with high rate of mortality. Starting early TB treatment may decrease the mortality rate associated to ARV medications to increase CD4 count.

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