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Volume 14, Number 9—September 2008

Dispatch

Diagnostic Challenges of Central Nervous System Tuberculosis

Laura J. ChristieComments to Author , Ann M. Loeffler, Somayeh Honarmand, Jennifer M. Flood, Roger Baxter, Susan Jacobson, Rick Alexander, and Carol A. Glaser
Author affiliations: California Department of Public Health, Richmond, California, USA (L.J. Christie, S. Honarmand, J.M. Flood, C.A. Glaser); Children’s Hospital and Research Center at Oakland, Oakland, California, USA (L.J. Christie); Legacy Emanuel Children’s Hospital, Portland, Oregon, USA (A.M. Loeffler); Francis J. Curry National Tuberculosis Center, San Francisco, California, USA (A.M. Loeffler); Kaiser Oakland Medical Center, Oakland (L.J. Christie, R. Baxter); Kaiser Fremont Medical Center, Fremont, California, USA (S. Jacobson); Contra Costa County Public Health Laboratory, Martinez, California, USA (R. Alexander);

Suggested citation for this article

Abstract

Central nervous system tuberculosis (TB) was identified in 20 cases of unexplained encephalitis referred to the California Encephalitis Project. Atypical features (encephalitic symptoms, rapid onset, age) and diagnostic challenges (insensitive cerebrospinal fluid [CSF] TB PCR result, elevated CSF glucose levels in patients with diabetes, negative result for tuberculin skin test) complicated diagnosis.

Tuberculosis (TB) of the central nervous system (CNS) is classically described as meningitis. However, altered mental status, including encephalitis, is within the spectrum of clinical manifestations. Because early treatment can dramatically improve outcomes, consideration of TB as a potential pathogen in CNS infections, including encephalitis, is vital. The California Encephalitis Project (CEP), initiated in 1998 to study the causative agents, epidemiology, and clinical features of encephalitis, has identified 20 cases of culture-confirmed tuberculous encephalitis. In most instances, TB was not initially considered to be a likely cause.

The Study

Referrals are received by the CEP statewide from clinicians seeking diagnostic testing for immunocompetent patients, including TB PCR testing when appropriate, who meet the CEP case definition of encephalitis (1). Mycobacterial testing was often also conducted by the referring hospital. Inclusion criteria for this report were a positive cerebrospinal fluid (CSF) culture for Mycobacterium tuberculosis complex or a positive CSF TB PCR result. Clinical data were compiled from case history forms and other medical records when available. To evaluate differences among causes of encephalitis, TB patients were compared with CEP patients with cases of enterovirus and herpes simplex virus 1 (HSV-1) encephalitis. Demographic, clinical, and laboratory data were compared by using the Fisher exact test, χ2 test, or Kruskal-Wallis test as appropriate (statistical significance was set at α = 0.05).

From June 1998 through October 2005, a total of 1,587 patients were enrolled in the CEP; 20 patients fulfilled criteria as TB cases. Demographic and clinical information for the study population are detailed in the Appendix Table [PDF - 22 KB - 2 pages]. Median age was 41 years (range 8 months to 77 years). The median time from symptom onset to first lumbar puncture was 5 days (range 0–62 days). Seventeen patients (85%) had a second lumber puncture.

In general, CSF values became more abnormal over time, with increasing leukocyte counts and protein levels and decreasing glucose levels (Appendix Table [PDF - 22 KB - 2 pages]). Most patients had a CSF mononuclear cell predominance, although 4 patients (21%) had a neutrophil predominance. All patients had cranial neuroimaging, magnetic resonance imaging (18 of 20), and computed tomography (20 of 20) (Appendix Table [PDF - 22 KB - 2 pages]; Table). Results of computed tomography scans were often normal (50%).

Of patients in whom the results of a recent tuberculin skin test (TST) were known, 59% (10 of 17) had a negative result (Appendix Table [PDF - 22 KB - 2 pages]). Many chest radiographs (9 of 18, 50%) showed no abnormalities. Concurrent culture positive pulmonary disease was found in 4 (50%) of 8 patients tested. A history of foreign birth (53%) or foreign travel (80%) was common. When these factors were reported, 5 patients (25%) had a history of treatment for TB and 5 patients (63%) had contact with a known case of TB. Only 2 patients did not have at least 1 of these risk factors.

Of the 20 cases identified, all had a positive CSF culture for M. tuberculosis complex. Only 4 (24%) of 17 were CSF TB PCR positive and none had a positive CSF acid-fast bacilli smear (Appendix Table [PDF - 22 KB - 2 pages]). All but 3 patients had pan-susceptible M. tuberculosis isolates; 2 patients had M. bovis isolates (resistant to pyrazinamide) and 1 patient had an isoniazid-resistant isolate.

When patients with TB were compared with patients with viral causes of encephalitis (Table), those with enterovirus encephalitis were significantly younger, were less likely to require intensive care, had shorter hospitalizations, had fewer abnormal results for CSF and neuroimaging, and were less likely to die (all p<0.05). Patients with HSV-1 encephalitis were more likely than those with CNS TB to be white and non-Hispanic and to have shorter hospital stays, lower CSF leukocyte and protein levels, and higher CSF glucose levels.

Conclusions

Although tuberculous meningitis is well described, prominent encephalitic features are less commonly reported. Illness and death associated with neurotuberculosis are highly dependent on the stage of disease at diagnosis; early diagnosis and treatment correlates with better outcomes (2). Although the TB cases reported here represent only a small percentage of CEP cases (<1%), CNS TB with an encephalitic picture warrants further discussion because of high morbidity and mortality rates and need for early diagnosis and appropriate treatment.

This study found atypical features of CNS disease that may have confounded early diagnosis. Tuberculous CNS disease is typically described as a chronic meningitis with insidious onset in children <5 years of age or in older adults with relatively few cases during school age years or adolescence (3). In contrast, CEP TB patients came to a hospital within 2 weeks of symptom onset and the greatest percentage of CEP TB patients was found in persons 10–19 years of age (22%).

Although typical CSF studies (mononuclear cell pleocytosis, low glucose levels, and elevated protein levels) (4) were often found in CEP CNS TB patients, atypical findings were noted. CSF glucose levels were often normal in patients with diabetes, although the ratio of CSF to serum glucose was invariably low. Additionally, a CSF neutrophil predominance was found in 4 patients, erroneously suggesting pyogenic meningitis. Although clinicians may be tempted to ascribe abnormal CSF values to viral meningitis or encephalitis based on abnormal CSF values, CEP patients with enterovirus and HSV-1 encephalitis rarely had glucose levels <40 mg/dL. Median protein levels were significantly higher in patients with CNS tuberculosis (174 mg/dL in TB) than in patients infected with HSV-1 (71 mg/dL) or enterovirus (60 mg/dL) (p<0.001).

Diagnostically, the low sensitivity of CSF TB PCR is problematic. Potential explanations for the lack of sensitivity in CSF specimens include low bacillary load in CSF, small sample volumes, and PCR inhibitors in the sample (5). Given that all of our patients had positive CSF cultures, we would have expected a higher PCR yield. Most concerning was the finding that many providers caring for these patients were dissuaded from pursuing TB as a diagnostic possibility when the PCR result was negative.

Given the difficulties in obtaining a rapid diagnosis, therapy must often be initiated empirically. Unfortunately, a history of TB and TST or chest radiograph results were not reliable indicators of active disease and might be difficult to obtain. Further complicating therapy, lengthy cultures, and isolate sensitivities are necessary to optimize choices of antimicrobial drugs. Ten percent (2) of our patients were infected with M. bovis, a relatively higher percentage than in other reports (68). Intrinsic pyrazinamide resistance (9) of M. bovis required modification of use of empiric antimicrobial drugs.

A limitation of this series is inclusion of only patients with a positive CSF culture. Because historical data suggest that only 25%–70% of patients with a diagnosis of CNS TB have a diagnosis confirmed by microbiologic testing (2), there were likely additional CEP patients with CNS tuberculous disease without a positive acid-fast bacilli culture who were not included in this series. Additionally, the series was limited by the referral bias inherent in the project; CEP patients are typically sicker and present greater diagnostic challenges. Thus, those with obvious or mild CNS tuberculous disease would be underrepresented. Despite this potential bias, outcomes were similar (mortality rate 30%) compared with reported mortality rates (18%–72%) and morbidity rates (16%–48%) in previous studies (10).

This report emphasizes some atypical features of CNS TB manifested as encephalitis. Encephalopathic changes, a relatively rapid course, nonclassic age distribution, and negative TB PCR and TST results should not dissuade a clinician from considering TB, particularly when CSF:serum glucose ratio (11) is <0.5 and CSF protein level is >100 mg/dL. The CEP TB patients reported here may represent a severe part of the continuum of TB meningitis or may represent a distinct encephalitic subset with atypical features.

Dr Christie is a hospital-based pediatric specialist at Kaiser Oakland Medical Center. Her research interests include M. tuberculosis, Epstein-Barr virus, Mycoplasma pneumoniae–associated encephalitis, and pediatric West Nile Virus infections.

Acknowledgments

We thank the clinicians for referring patients to the California Encephalitis Project and the laboratory staff in the Viral and Rickettsial Disease Laboratory (Richmond, CA) and Microbial Disease Laboratory (Richmond) as well as the Contra Costa County Public Health Laboratory (Martinez, CA) for performing diagnostic testing.

This study was supported by the Centers for Disease Control and Prevention Emerging Infections Program (grant no. U50/CCU915546-09).

References

  1. California Emerging Infections Program, California Encephalitis Project, Enhanced Diagnostic Testing and Epidemiology. Oakland (CA): The Program [cited 2007 Nov 28]. Available from http://www.ceip.us/encephalitis.htm
  2. Garg RK. Tuberculosis of the central nervous system. Postgrad Med J. 1999;75:13340.PubMed
  3. Thwaites G, Chau TTH, Mai NTH, Drobniewski F, McAdam K, Farrar J. Tuberculous meningitis. J Neurol Neurosurg Psychiatry. 2000;68:28999. DOIPubMed
  4. Klein NC, Damsker B, Hirshman SZ. Mycobacterial meningitis: retrospective analysis from 1970 to 1983. Am J Med. 1985;79:2934. DOIPubMed
  5. Pai M, Flores LL, Pai N, Hubbard A, Riley LW, Colford JM Jr. Diagnostic accuracy of nucleic acid amplification tests for tuberculous meningitis: a systematic review and meta-analysis. Lancet Infect Dis. 2003;3:63343. DOIPubMed
  6. Centers for Diseease Control and Prevention. Human tuberculosis caused by Mycobacterium bovis—-New York City, 2001–2004. MMWR Morb Mortal Wkly Rep. 2005;54:6058.PubMed
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  8. Dankner WM, Davis CE. Mycobacterium bovis as a significant cause of tuberculosis in children residing along the United States–Mexico border in the Baja California region. Pediatrics. 2000;105:E79. DOIPubMed
  9. de Jong BC, Onipede A, Pym AS, Gagneuz S, Aga RS, DeRiemer K, Does resistance to pyrazinamide accurately indicate the presence of Mycobacterium bovis? J Clin Microbiol. 2005;43:35302. DOIPubMed
  10. Girgis NI, Sultan Y, Farid Z, Mansour MM, Erian MW, Hanna LS, Tuberculosis meningitis, Abbassia Fever Hospital–Naval Medical Research Unit No. 3–Cairo, Egypt, from 1976 to 1996. Am J Trop Med Hyg. 1998;58:2834.PubMed
  11. Newton RW. Tuberculous meningitis. Arch Dis Child. 1994;70:3646.PubMed

Tables

Suggested citation for this article: Christie LJ, Loeffler AM, Honarmand S, Flood JM, Baxter R, Jacobson S, et al. Diagnostic challenges of central nervous system tuberculosis. Emerg Infect Dis [serial on the Internet]. 2008 Sep [date cited]. Available from http://wwwnc.cdc.gov/eid/article/14/9/07-0264

DOI: 10.3201/eid1409.070264

Table of Contents – Volume 14, Number 9—September 2008

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