At the age of 19, I underwent surgery for a unilateral vestibular schwannoma (4mm)?
As per the title, I had surgery three years ago, and during my one-year follow-up, there was no recurrence.
The doctor mentioned that I could follow up again in five years.
I should have felt relieved, but after researching some information online, I found that sporadic vestibular schwannomas typically occur in older age groups.
If they occur in younger individuals, it could potentially be Neurofibromatosis Type 2 (NF2).
However, I have never experienced the symptoms mentioned in the literature, and prior to the surgery, the MRI only revealed the vestibular schwannoma.
Since the surgery, I have not experienced any other symptoms.
The doctor previously stated that the surgery was very successful and that my recovery was good during follow-ups, but I am still quite worried.
I would like to ask: Can NF2 be determined from the postoperative tissue analysis report? Should I undergo any genetic testing? Or am I just overthinking this? Please clarify.
Thank you.
Winnie, 20~29 year old female. Ask Date: 2011/08/09
Dr. Ding Xianwei reply Neurosurgery
NF2 has specific criteria; if you do not meet these criteria, you should not be diagnosed with NF2.
I think you do not need to worry too much, just ensure proper monitoring.
Reply Date: 2011/08/09
More Info
Neurofibromatosis Type 2 (NF2) is a genetic disorder characterized by the development of bilateral vestibular schwannomas (also known as acoustic neuromas) and other tumors of the nervous system. It is important to understand that NF2 is typically inherited in an autosomal dominant manner, meaning that a person only needs one copy of the mutated gene from one parent to be affected. The average age of onset for symptoms related to NF2 is often in the late teens to early adulthood, but it can vary widely.
In your case, having undergone surgery for an acoustic neuroma three years ago, and with no recurrence noted during your follow-up, is a positive sign. The fact that your doctors have advised a five-year follow-up indicates that they are confident in your recovery. However, your concerns about NF2 are understandable, especially given the information you found online regarding the typical age of onset for sporadic acoustic neuromas.
Regarding your specific questions:
1. Can NF2 be detected in post-operative tissue analysis?
Yes, NF2 can sometimes be identified through genetic testing or histopathological examination of the tumor tissue. If the tumor shows specific characteristics or if there is a family history of NF2, further genetic testing may be warranted. However, if your tumor was a solitary acoustic neuroma without any other associated tumors or symptoms, it is less likely that NF2 is present.
2. Should you undergo genetic testing?
If you have concerns about NF2, particularly if you have a family history of the condition or if you develop new symptoms, discussing genetic counseling with your healthcare provider may be beneficial. Genetic testing can provide clarity regarding your risk for NF2 and help guide future monitoring and management.
3. Are you overthinking this?
It is natural to feel anxious after a significant medical event like surgery, especially when faced with the potential implications of a genetic disorder. However, it is essential to focus on the information provided by your healthcare team. If your doctors have not indicated any signs of NF2 and have reassured you about your recovery, it may be helpful to trust their expertise.
In summary, while NF2 is a valid concern for individuals with a history of acoustic neuromas, your current situation—having had a successful surgery with no recurrence—suggests that you may not be affected by NF2. Regular follow-ups as recommended by your physician are crucial for monitoring your health. If you have persistent concerns, consider discussing them with your healthcare provider, who can offer personalized advice based on your medical history and current health status.
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