S. Kawamura et al., INTRAMEATAL TUMORS PRESENTING AS A HEARING DISTURBANCE - CASE-REPORTSOF MENINGIOMA AND LYMPHOMA, Acta neurochirurgica, 140(7), 1998, pp. 675-679
This paper presents two patients with chronic progressive hearing dist
urbance. Each patient had an intrameatal tumour, part of which extende
d to the cerebellopontine (CP) angle. In both cases, the patients were
initially diagnosed with an acoustic neurinoma. A 63-year-old male ex
perienced a hearing disturbance in the left ear for 1.5 years prior to
visiting our hospital. Magnetic resonance (MR) imaging revealed a mas
s which was surgically resected. The tumour originated from the intram
eatal dura mater. Histologically, the tumour was a meningioma. Similar
ly, a 53-year-old male presented with systemic lymphoma diagnosed 10 m
onths earlier, and a hearing disturbance in the right ear that began 3
months prior to visiting our hospital. MR imaging prior to chemothera
py revealed a mass which extended to the CP angle. Part of the tumour
in the CP angle disappeared after chemotherapy, suggesting a secondary
lymphoma. Another tumour appeared later in Meckel's cave on the left
side; however, it decreased in size following repeated chemotherapy. T
he present results indicate that differential diagnosis of intrameatal
tumours and acoustic neurinomas may be difficult due to the small tum
our size. Recent progress in neuroradiology may allow distinction of i
ntrameatal rumours as a separate tumour classification. Our second pat
ient is the sixth reported case of a CP angle lymphoma in the literatu
re.