Abstract
Acute onset of diplopia associated with high-grade fever, sore throat and cough without features of raised intracranial tension in a young patient is an uncommon presentation. A diagnosis of abducent nerve palsy due to pontine tuberculoma associated with miliary tuberculosis was made based on sputum examination, chest x-ray and MRI. On diagnosis, monocular patching of the left eye was performed to avoid diplopia and primary antitubercular drugs with systemic steroids were given. An unfortunate 48 h delay in starting the antitubercular treatment likely decreased the probability of survival.
Case presentation
A 20-year-old man presented to the ophthalmology outpatient department of our rural hospital attached to our medical college with chief complaints of diplopia, high-grade fever (39°C) with sore throat and cough.
The patient appeared moderately built and poorly nourished, with no history of any premorbid illness. His best-corrected visual acuity recorded was 20/20 (Snellen chart) in both eyes. Ocular positioning tests revealed an esotropia (30∆ D) for distance and esotropia (60∆ D) for near in primary position. Esotropia increased with horizontal gaze to the left (gaze towards the affected eye). The ductions of the right eye were normal, whereas the left eye showed limited abduction with associated face turn towards the left. No vertical deviations were present. Diplopia charting confirmed horizontal diplopia in the primary position and levoversion. Maximum separation was present in levoversion. Gross observations of the anterior segments of both eyes were normal. His pupils were brisk equally to light and accommodation. Dilated funduscopy was unremarkable, with no evidence of papilloedema.
A medical consultation revealed a congested pharynx and an essentially normal respiratory system examination. A neurological examination of the other cranial nerves and peripheral nerves was unremarkable. In view of the short duration of illness and predominant upper respiratory involvement, a possible diagnosis of viral pharyngitis with postviral abducens palsy was considered. However, other causes such as tuberculosis, neoplasms and autoimmune diseases needed to be ruled out.
Investigations
Diagnostic tests including a complete blood count, erythrocyte sedimentation rate (ESR) and sputum tests were ordered. Results of a haemogram showed a markedly elevated ESR of 105 mm/h and a white cell count of 12 800 cells/mm3 with 56% lymphocytes. Other parameters such as blood glucose, liver function tests and renal function tests were normal. Results of a HIV monospot were negative.
A chest x-ray could not be performed on that day as the machine was being upgraded in the hospital and the facility was hence unavailable.
Our patient had to be transferred to a higher centre, about 30 km away, for a chest x-ray and MRI scan of the brain. The appointment for an MRI was given the next day. Our patient returned with a chest x-ray that showed bilateral miliary mottling.
The MRI of the brain, plain and with contrast, revealed an ill-defined hyperintense lesion on T2 (TR-5250, TE-112), fluid-attenuated inverse recovery (TR-13000, TE-112) sequences, measuring 11×12 mm involving the pons on the left side with perilesional oedema and mild effacement of the fourth ventricle. On postcontrast T1 (TR-465, TE-17) images, a ring-enhancing lesion was noted within this area of altered signal intensity. The rest of his brain parenchyma showed normal signal intensity with preserved grey/white matter differentiation. The orbits appeared normal. There were no signs of raised intracranial tension.
Sputum test results were positive for acid-fast bacilli. On the basis of these findings, a lateral rectus palsy due to left-sided pontine tuberculoma in a patient with miliary tuberculosis was diagnosed.1
Treatment
The patient was not willing to be admitted to our hospital for treatment, but preferred to go a regional government hospital where tuberculosis treatment would be given free of cost. The next day, he was started on four primary antitubercular drugs, along with systemic steroids and symptomatic treatment.
Outcome and follow-up
Unfortunately, our patient died on the seventh day after commencement of treatment.
Discussion
A young patient diagnosed as having abducent nerve palsy should have an urgent investigation of laboratory studies such complete blood cell count, glucose levels, glycosylated haemoglobin, ESR, C-reactive protein and anti-nuclear antibody test. A timely chest x-ray and neurological imaging studies are also needed. Lumbar puncture should also be considered if MRI results are negative.
Patients older than 40 years require a less aggressive investigation because of the greater likelihood of the aetiology being more benign in nature (eg, ischemic mononeuropathy, vasculopathy) due to conditions such as diabetes mellitus or hypertension.2
There has been one case report in the English literature of a 38-year-old man with an isolated ocular motility abnormality as presenting feature due to pontine tuberculoma, with the chest x-ray showing bilateral apical parenchymal infiltrates and consolidation and bilateral hilar lymphadenopathy where some reduction in the size of the tuberculoma after 1 month of treatment was noted.3 4
Learning points.
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In countries where tuberculosis is endemic, it should be suspected even in short duration illnesses.
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A simple investigation such as a chest x-ray, if performed immediately, can be very useful and life saving.
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Tuberculosis with neurological involvement, especially with short duration illness, can rapidly become fatal and treatment should be aggressive.
Footnotes
Competing interests None.
Patient consent Obtained.
References
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- 3.Saxena R, Menon V, Sinha A, et al. Pontine tuberculoma presenting with horizontal gaze palsy. J Neuroophthalmol 2006;26:276–8 [DOI] [PubMed] [Google Scholar]
- 4.Kent SJ, Crowe SM, Yung A, et al. Tuberculous meningitis: a 30-year review. Clin Infect Dis 1993;17:987–94 [DOI] [PubMed] [Google Scholar]
