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Neurology Research International
Volume 2017, Article ID 2854043, 4 pages
https://doi.org/10.1155/2017/2854043
Research Article

Increased Intracranial Pressure in the Setting of Enterovirus and Other Viral Meningitides

The Saul R. Korey Department of Neurology, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, USA

Correspondence should be addressed to Jules C. Beal; gro.eroifetnom@laebj

Received 1 August 2016; Accepted 14 December 2016; Published 12 April 2017

Academic Editor: Rod Scott

Copyright © 2017 Jules C. Beal. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Increased intracranial pressure due to viral meningitis has not been widely discussed in the literature, although associations with Varicella and rarely Enterovirus have been described. Patients with increased intracranial pressure and cerebrospinal fluid analysis suggestive of a viral process are sometimes classified as having atypical idiopathic intracranial hypertension (IIH). However, a diagnosis of IIH requires normal cerebrospinal fluid, and therefore in these cases an infection with secondary intracranial hypertension may be a more likely diagnosis. Here seven patients are presented with elevated intracranial pressure and cerebrospinal fluid suggestive of viral or aseptic meningitis. Of these, 1 had Enterovirus and the remainder were diagnosed with nonspecific viral meningitis. These data suggest that viral meningitis may be associated with elevated intracranial pressure more often than is commonly recognized. Enterovirus has previously been associated with increased intracranial pressure only in rare case reports.

1. Introduction

Infections involving the central nervous system have an established association with increased intracranial pressure (ICP). Bacterial meningitis and central nervous system involvement of tuberculosis, for example, are well-described to lead to elevations of ICP, as are fungal infections [13]. Less frequently, increased pressures have been reported in association with Lyme disease [4]. There is a general paucity of information in the literature regarding viral meningitis as a cause of increased ICP, although cases associated with Varicella [5] and very rarely Enterovirus infection [6, 7] have been described. Patients with elevated intracranial pressure and a cerebrospinal fluid (CSF) profile suggestive of an infectious process in the absence of any of these known infectious causes are sometimes characterized as having a nonspecific viral syndrome [8] or an atypical presentation of idiopathic intracranial hypertension (IIH, also known as pseudotumor cerebri). The clinical definition of IIH has been updated and revised multiple times, but all definitions have specified that in order to make a diagnosis of IIH there must be a normal CSF profile [911]. Therefore patients with CSF analysis suggestive of an infectious process cannot be given a diagnosis of idiopathic intracranial hypertension; more likely these patients have aseptic or viral meningitis. The purpose of this paper is to report a series of patients seen by the inpatient pediatric neurology service at a tertiary care children’s hospital who were found to have increased ICP and a CSF profile suggestive of viral meningitis. The frequency with which these patients were encountered suggests that viral meningitis may be associated with elevated intracranial pressure more often than is commonly recognized.

2. Methods

A retrospective chart review looking for cases of viral meningitis with associated elevation of intracranial pressure was performed. Cases with a diagnosis of viral meningitis, aseptic meningitis, idiopathic intracranial hypertension, or pseudotumor cerebri were identified from an existing database of all patients seen by the inpatient pediatric neurology consultation service over the five-year period from July 1, 2009, to June 30, 2014. These charts were then reviewed to identify patients who had an elevated opening pressure during lumbar puncture, defined for screening purposes as greater than 20 centimeters of water (cm H2O) [10], as well as an elevated white blood cell count on CSF analysis with lymphocytic predominance. Those with evidence of bacterial meningitis (including neutrophil predominance, low CSF glucose, and/or positive bacterial cultures) were excluded. Those with evidence of viral meningitis without documentation of elevated opening pressure during lumbar puncture were excluded. Patients with abnormal findings on brain imaging that could potentially contribute to elevations in intracranial pressure were excluded. Patients presenting with confusion or altered mental status were excluded as these findings may suggest meningoencephalitis, which is more commonly known to cause elevations in intracranial pressure [12].

3. Results

Overall, 44 patients with a diagnosis of aseptic meningitis and 81 patients with a diagnosis of intracranial hypertension were identified. Thirteen patients met both criteria. Four of these were excluded due to the presence of confusion or altered mental status. One was excluded due to evidence of Lyme disease and one was excluded due to evidence of Rocky Mountain Spotted Fever, as these are both bacterial infections. The remaining seven patients ranged in age from 10 to 19 years old. Five of the seven were male. Patient demographics and presenting symptoms are shown in Table 1. All patients complained of headache on presentation. Three of the seven had nausea and vomiting, three had neck pain or neck stiffness, three complained of blurred vision, and one had fever on presentation. Three of the seven patients had documented papilledema, and one was documented to not have papilledema. The remaining three patients did not have a documented fundoscopic exam. All patients had unremarkable brain imaging.

Table 1: Patient demographics and presenting symptoms.

Table 2 shows the opening pressures and results of CSF testing for each of the seven patients. All patients had pressures above 20 cm H2O, ranging from 21 cm H2O to greater than 55 cm H2O, which is the highest measurable pressure on the manometer. All patients had elevated white blood cell counts in the CSF, ranging from 13 to 270 cells/μL (normal defined as less than 13 cells/μL), each with 60% lymphocytes or greater. Four of the patients had clearly elevated protein levels in the CSF (normal range defined as 10–41 mg/dL).

Table 2: Results of lumbar puncture and cerebrospinal fluid testing.

All patients had negative bacterial cultures. Polymerase chain reaction (PCR) for Enterovirus was performed in six patients and was positive in one patient. Though Lyme titers were positive in one patient, this patient subsequently had a negative immunoblot for Lyme disease. Cryptococcal antigen testing was performed in two patients and was negative in both. Cultures for acid fast bacilli were negative in two patients. One patient had negative PCR for herpes simplex virus, one had negative fungal cultures, and one had negative testing for Bartonella.

All patients had resolution of their presenting symptoms at discharge. Five of the seven patients were subsequently lost to follow-up. The remaining two patients (patients numbers 2 and 4) who continued to be seen within the hospital system did not suffer from chronic headaches, vision loss, or other long term neurologic sequelae.

4. Discussion

The definition of elevated ICP in children has not been well established. Almost certainly, “normal” pressures exist on a spectrum in which the same pressure may be the normal baseline in some children but pathologically elevated in others. A measured pressure of 20 cm H2O, used here for screening purposes, has traditionally been considered the upper limit of normal [10]. Some authors have proposed that pressures of 25 cm H2O may be normal, especially in obese patients [13, 14], or that pressures between 20 and 25 cm H2O may be nondiagnostic [15]. It has been suggested that pressures as high as 28 cm H2O may be normal in pediatric patients, and revised diagnostic criteria for IIH using a pressure of 28 cm H2O as the upper limit of normal in children have been proposed [11]. According to these revised criteria, three of the patients described above would not be considered to have elevated ICP: patients 2, 6, and 7 all had opening pressure less than 28 cm H2O. Patients 6 and 7, however, both had papilledema which would suggest that their pressures were elevated relative to their normal baseline. Patient 2 was the only patient to have confirmed absence of papilledema, and therefore a diagnosis of increased ICP in this patient may be debatable.

The diagnostic criteria for Idiopathic Intracranial Hypertension have been revised multiple times. All definitions, though, specify that the diagnosis of IIH requires a normal CSF profile, normal brain parenchyma on imaging, and a normal neurologic exam with the exception of cranial nerve abnormalities referable to increased ICP, for example, a sixth cranial nerve palsy [911]. Patients who otherwise meet criteria for a diagnosis of IIH but are found to have a CSF leukocytosis, however, likely have a secondary intracranial hypertension due to an infectious process rather than true IIH. A similar series of patients has previously been published with presumed viral meningitis-induced intracranial hypertension [8], but in general this type of nonspecific infectious etiology often goes unreported. Other infections leading to intracranial hypertension, in contrast, are widely recognized, most notably with bacterial, fungal, and tuberculous meningitis or meningoencephalitis [13], as well as Lyme disease [4], and viral encephalitis [12]. Increased intracranial pressure due to viral meningitis is less commonly identified, although associations with Varicella and very rarely Enterovirus have been described [57]. The patients described here all had CSF profiles suggestive of an infectious process, including leukocytosis with a lymphocytic predominance and, in several cases, clearly elevated CSF protein. In the absence of symptoms of encephalitis, these findings suggest that these patients likely had viral meningitis with secondary elevations in intracranial pressure [16].

The infectious workup performed on these patients was widely variable, emphasizing the need to standardize the way in which these patients are assessed. Lyme disease titers were only tested in three of the seven patients and cultures for acid-fast bacilli were only performed in two and fungal culture in one. None of the patients were tested for Varicella. On the other hand, six of the seven patients were tested for Enterovirus. Enterovirus has been associated with elevated intracranial pressure, but only in very rare case reports [6, 7]. Thus patient 2 may represent a rarely reported entity, although this is also the patient in whom the diagnosis of intracranial hypertension may be debatable, as discussed above.

5. Conclusions

While certain infections of the central nervous system are known to lead to elevated intracranial pressure, viral meningitis as a cause of increased ICP is much less commonly described. The seven patients described here with elevated ICP and lymphocytic leukocytosis in the CSF do not meet diagnostic criteria for idiopathic intracranial hypertension but rather have secondary intracranial hypertension as a result of viral meningitis. This suggests that this entity may be more common than is typically recognized. Varicella and to a lesser extent Enterovirus have been associated with increases in ICP. Therefore, in patients with clinical signs of meningitis, elevated opening pressures on lumbar puncture and CSF lymphocytosis, testing for Varicella and Enterovirus in addition to Lyme disease and tuberculosis, may be useful. The utility of testing for other viral etiologies is unclear. Other specific viral causes of meningitis have not been clearly associated with elevated intracranial pressure in the literature. However the fact that this and other papers have reported associations between intracranial hypertension and a nonspecific, presumably viral, meningitis suggests that there are likely other causative organisms that may potentially be identified with more extensive testing.

Ethical Approval

This study was granted a status of “Exempt” by the Albert Einstein College of Medicine Internal Review Board.

Competing Interests

The author declares that there is no conflict of interests regarding the publication of this paper.

References

  1. P. Lepage and B. Dan, “Infantile and childhood bacterial meningitis,” Handbook of Clinical Neurology, vol. 112, pp. 1115–1125, 2013. View at Publisher · View at Google Scholar · View at Scopus
  2. R. Raman Sharma, “Fungal infections of the nervous system: current perspective and controversies in management,” International Journal of Surgery, vol. 8, no. 8, pp. 591–601, 2010. View at Publisher · View at Google Scholar · View at Scopus
  3. A. A. Figaji and A. G. Fieggen, “The neurosurgical and acute care management of tuberculous meningitis: evidence and current practice,” Tuberculosis, vol. 90, no. 6, pp. 393–400, 2010. View at Publisher · View at Google Scholar · View at Scopus
  4. L. Kan, S. K. Sood, and J. Maytal, “Pseudotumor cerebri in Lyme disease: a case report and literature review,” Pediatric Neurology, vol. 18, no. 5, pp. 439–441, 1998. View at Publisher · View at Google Scholar
  5. S. Ravid, Y. Shachor-Meyouhas, E. Shahar, Z. Kra-Oz, and I. Kassis, “Reactivation of varicella presenting as pseudotumor cerebri: three cases and a review of the literature,” Pediatric Neurology, vol. 46, no. 2, pp. 124–126, 2012. View at Publisher · View at Google Scholar · View at Scopus
  6. K. H. Kim, “Enterovirus 71 infection: an experience in Korea, 2009,” Korean Journal of Pediatrics, vol. 53, no. 5, pp. 616–622, 2010. View at Publisher · View at Google Scholar · View at Scopus
  7. P. McMinn, I. Stratov, L. Nagarajan, and S. Davis, “Neurological manifestations of enterovirus 71 infection in children during an outbreak of hand, foot, and mouth disease in Western Australia,” Clinical Infectious Diseases, vol. 32, no. 2, pp. 236–242, 2001. View at Publisher · View at Google Scholar · View at Scopus
  8. S. Ravid, Y. Shachor-Meyouhas, E. Shahar, Z. Kra-Oz, and I. Kassis, “Viral-induced intracranial hypertension mimicking pseudotumor cerebri,” Pediatric Neurology, vol. 49, no. 3, pp. 191–194, 2013. View at Publisher · View at Google Scholar · View at Scopus
  9. W. E. Dandy, “Intracranial pressure without brain tumor: diagnosis and treatment,” Annals of Surgery, vol. 106, no. 4, pp. 492–513, 1937. View at Publisher · View at Google Scholar
  10. A. K. Ball and C. E. Clarke, “Idiopathic intracranial hypertension,” Lancet Neurology, vol. 5, no. 5, pp. 433–442, 2006. View at Publisher · View at Google Scholar · View at Scopus
  11. D. I. Friedman, G. T. Liu, and K. B. Digre, “Revised diagnostic criteria for the pseudotumor cerebri syndrome in adults and children,” Neurology, vol. 81, no. 13, pp. 1159–1165, 2013. View at Publisher · View at Google Scholar · View at Scopus
  12. G. Kumar, J. Kalita, and U. K. Misra, “Raised intracranial pressure in acute viral encephalitis,” Clinical Neurology and Neurosurgery, vol. 111, no. 5, pp. 399–406, 2009. View at Publisher · View at Google Scholar · View at Scopus
  13. J. J. Corbett and M. P. Mehta, “Cerebrospinal fluid pressure in normal obese subjects and patients with pseudotumor cerebri,” Neurology, vol. 33, no. 10, pp. 1386–1388, 1983. View at Publisher · View at Google Scholar · View at Scopus
  14. J. Hannerz, D. Greitz, and K. Ericson, “Is there a relationship between obesity and intracranial hypertension?” International Journal of Obesity, vol. 19, no. 4, pp. 240–244, 1995. View at Google Scholar · View at Scopus
  15. D. I. Friedman and D. M. Jacobson, “Diagnostic criteria for idiopathic intracranial hypertension,” Neurology, vol. 59, no. 10, pp. 1492–1495, 2002. View at Publisher · View at Google Scholar · View at Scopus
  16. S. Pelc, E. De Maertelaere, and R. Denolin-Reubens, “CSF cytology of acute viral meningitis and meningoencephalitis,” European Neurology, vol. 20, no. 2, pp. 95–102, 1981. View at Google Scholar · View at Scopus