Neurology India Medknow Publications on behalf of the Neurological Society of India ISSN: 0028-3886 EISSN: 1998-4022 Vol. 52, Num. 3, 2004, pp. 401-402

Neurology India, Vol. 52, No. 3, July-September, 2004, pp. 401-402

Letter To Editor

Delayed tension pneumocephalus: A rare complication of shunt surgery

Sankhla Suresh, Khan GM, Khan MA

Department of Neurosciences, Prince Aly Khan Hospital, Aga Hall, Nesbit Road, Mazgaon, Mumbai - 400 010

Correspondence Address:Department of Neurosciences, Prince Aly Khan Hospital, Aga Hall, Nesbit Road, Mazgaon, Mumbai - 400 010
ssankhla@vsnl.com

Code Number: ni04138

Sir,
We report an unusual case of congenital hydrocephalus that developed acute tension pneumocephalus six months after the ventriculo-peritoneal shunt surgery. Delayed and symptomatic pneumocephalus following shunt placement is rare and has been described in only 11 cases so far.[1],[2],[3],[4],[5],[6],[7],[8],[9],[10],[11]

A 19-year-old female had undergone ventriculo-peritoneal shunt surgery for obstructive hydrocephalus secondary to congenital aqueduct stenosis. Six months later, she presented with sudden onset of severe headache followed by altered sensorium. A computed tomographic (CT) scan of brain showed large pneumocephalus involving the right frontal lobe, basal cisterns, and the lateral and third ventricles [Figure - 1]. Further assessment with high-resolution coronal CT and MRI did not demonstrate any defect at the skull base but an area of gliosis and porencephalic cyst was discovered in the right frontal lobe adjacent to the suspected site of leakage in the right frontal air sinus [Figure - 2]. On exploration with a right frontal craniotomy, a fistulous opening was identified in the posterior wall of the right frontal air sinus and in the adjacent dura of the frontal region. A watertight dural repair was performed using a pericranial graft and the right frontal sinus was exenterated, packed with adipose tissue, and covered with the pericranium of the frontal base. Her postoperative recovery was uneventful, and she was asymptomatic at a follow-up after 24 months.

The mechanism of development of pneumocephalus is mainly based on two factors - a reduction in intracranial pressure (ICP), and the presence of a defect in the dura and skull.[10] A long-standing elevation in ICP due to hydrocephalus has been reported to cause erosion of the skull base.[9] It appears that patients can remain asymptomatic as long as the defect is completely plugged by meningeal scarring or gliosed brain tissue that acts as a ball-valve. Significant lowering of intracranial pressure following shunting, causes unplugging of the defect that results in the opening up of the fistula.

The clinical management is essentially based on the treatment of acute intracranial hypertension, therapy or prophylaxis of meningitis, shunt management, and repair of the fistula. Although, intracranial air often resolves spontaneously,[2] tension pneumocephalus causing acute elevation of ICP requires immediate measures to release the entrapped air by simple aspiration or continuous external drainage.[5],[7] There is general agreement that externalization of the shunt should be done if infection is present or a viscus is perforated. Shunt management in the presence of a sterile and well functioning shunt is controversial. Although, successful management of pneumocephalus has been reported with modifications in the shunt system alone,[6],[9],[11] most believe that the treatment should mainly be aimed at direct surgical closure of the site of air entry, and that any change in a normally functioning shunt is unnecessary.[1],[2],[7],[10] Smaller and multiple fistulous tracts at the skull base are difficult to diagnose and are frequently associated with recurrent pneumocephalus or meningitis.[2] When a porencephalic cyst is present, as in our case, the identification of a fistulous defect is relatively easier because of its close proximity with the cyst.[1],[3],[10] Recent techniques with three-dimensional CT scan are more accurate and useful to locate the skull base defects.[11]

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