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Neurology India
Medknow Publications on behalf of the Neurological Society of India
ISSN: 0028-3886 EISSN: 1998-4022
Vol. 52, Num. 3, 2004, pp. 402-402
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Neurology India, Vol. 52, No. 3, July-September, 2004, pp. 402
Letter To Editor
Recurrent oculomotor nerve palsy: A rare presentation of neurocysticercosis
Mokta JK, Mahajan Sanjay, Machhan Prem, Mokta KiranK, Patial RK, Prashar BS
Departments of Medicine, IGMC, Shimla
Correspondence Address:Departments of Medicine, Dr. Rajendra Prasad Medical College and Hospital, Tanda, H. P
Code Number: ni04139
Sir,
A non-diabetic, non-hypertensive, 34-year-old male presented with sudden
onset of complete ptosis of left eye and partial ptosis of right eye
of one day duration. He denied diplopia, headache, orbital pain, visual
impairment or any weakness of body. Three months ago, he had similar
symptoms, which recovered spontaneously by the fourth day. On examination,
there was complete ptosis on the left side and partial ptosis on the
right side. There was no nystagmus. The left pupil was larger (5.5mm)
than the right (3.5mm) and both pupils were non-reacting to light and
accommodation. No afferent pupillary defect was present. Fundoscopy revealed
no abnormality. Left eye movement was limited to abduction and intortion
on attempted down gaze. The right eye was moving fully except in the
direction of the superior rectus muscle. The rest of the neurological
examination was also normal. Magnetic resonance imaging (MRI) of the
brain revealed single ring enhancing lesion (11.6x9.7 x 11.11mm) with
perifocal edema and the central part of the lesion containing fluid (hypointense
on T1W1 and hyperintense on T2W2) at the tegmentum of the left midbrain
[Figure - 1]. The rest of the brain parenchyma, ventricular system and subarachnoid space was normal. The biochemical and cytological examination of CSF revealed protein of 50mg%, sugar of 40mg%, and 9 cells, all lymphocytes. Polymerase chain reaction (PCR) analysis of mycobacterium DNA was negative both in CSF and serum. Enzyme-linked immunosorbent assay (ELISA) for cysticercus was positive both in CSF and serum. X-Ray chest, thigh and arm were normal. The patient was treated only with edema-lowering agents and he recovered in his symptoms on the sixth day. Follow-up CT scan at four months revealed complete resolution of the granuloma. At one-year follow-up, the patient was completely asymptomatic.
The case demonstrates that midbrain cysticercosis may present with recurrent episodes of unilateral or bilateral third cranial nerve affection.
Copyright 2004 - Neurology India
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