Intracranial lipomas located in the cerebellopontine angle are extremely ra
re. These rumours are maldevelopmental lesions which can cause slowly proge
ssive neurological symptoms. The clinical management of these rumours diffe
rs significantly from other lesions in this region. A 27 year old woman pre
sented with a 2-month his tory of vertigo and a slowly progressive deterior
ation of hearing in the left ear. Computed tomography (CT) revealed a large
low-density mass in the left cerebellopontine angle without any contrast-e
nhancement. Ln T1-weighted magnetic resonance imaging (MRI) the lesion was
hyperintense and did not enhance after application of gadolinium. Areas of
lower signal intensity inside of the lesion were suggested as incorporated
cranial nerves. A left retrosigmoidal approach in a semi-sitting position w
as chosen to expose the tumour. After reducing the tumour mass, the tumour
was dissected from the cranial nerves which were incorporated into the tumo
ur. The residual tumour was adherent to the brain stem and the encased lowe
r cranial nerves, allowing only a near subtotal resection of the highly vas
cularized tumour in order to avoid neurological deficits. The histological
examination revealed a lipoma. Attempts at complete removal of cerebellopon
tine angle lipomas usually result in severe neurological deficits. Conserva
tive treatment should therefore be prefered. Limited surgery is indicated i
f the patients suffer from disabling neurological symptoms and signs e.g.,
vertigo, nausea, trigeminal neuralgia, facial weakness or facial spasm.