Schwannoma, also known as neurilemmoma, is a typically benign tumour that originates from the Schwann cells, which form the sheath around peripheral nerves.
These tumours can develop anywhere in the body but are most commonly found in the head, neck, and extremities, including within the inner ear canal, where they are known as acoustic neuromas.
Schwannomas are relatively uncommon. Worldwide, these tumours represent about 5% of all soft tissue tumours. In Singapore, the exact incidence is not well-documented but follows global rarity trends.
The symptoms of schwannoma depend on the tumour's location and size. Common symptoms include:
The precise cause of schwannomas is not fully understood. However, some cases are associated with genetic disorders such as neurofibromatosis type 2 (NF2), which involves a mutation in the NF2 gene on chromosome 22. This mutation leads to the loss of function of merlin, a tumour suppressor protein, resulting in tumour formation.
While schwannomas are usually benign and slow-growing, they can cause significant complications as they enlarge, including:
Currently, there are no known measures to prevent schwannomas, particularly because the specific causes are not completely understood. In individuals with neurofibromatosis, regular monitoring and early intervention can help manage the condition and prevent complications.
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