Late onset side effect (benign mucus cyst)

  • 8 replies
  • 50 subscribers
  • 1950 views

Hi

As many of you know I’m past 3 years for tonsil cancer with several affected lymph nodes and happily living our lives. At my last scheduled appointment 8 September in i waltzed on my own hubby in car. We were going away a week later and I hadn’t had a face to face since the previous December.Consultant did her usual visual checks then scoped . She discovered a small mucus filled cyst sitting in the top of vocal cord folds ( who  knew our vocal cords had folds ) bit like our tonsils having crypts! We learn so much having had cancer. 
We had a chat she wasn’t unduly concerned the offending cyst was 5 mm I didn’t know it was there it wasn’t causing any issues.I offered to postpone our trip,no way was her reply she wouldn’t do anything for 3 month anyway. So  off we drove to Spain cycled over 1100 km walked over 450 k m. 
No issues in fact I am lucky nothing stresses  me apart from the day I was put on cancer pathway.

Today was appointment day my hospital has a brand new digital scope that videos as well all in glorious HD. The cysts still there it’s not changed so we’ve agreed to a review at my next appointment which is 6 month now I am past 3 years. With the caveat if I feel I need to see her get in touch I will get an appointment. 

Am posting  just to let people know that late side effects may occur but our nhs is always there for us. 
Whats  caused it ,good old dry mouth lack of saliva passing over the vocal cords,have caused friction ,hence the cyst. So keep drinking water I still do 2 litres most days. 

  • Hi Hazel. Thanks for posting this. Mucous cysts are made because minor salivary ducts get blocked and a cyst forms. We have mucous glands all over our mouths and throats. 
    I too have encountered one which is in my throat. I found it and my oncologist confirmed it. So we are mucous cyst sisters JoyJoy

    They seem quite common 

    We are told to report anything that worries us and we are not wasting our clinicians time. I think we are largely pretty well looked after. 

    Dani 

    Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019

    Macmillan Support Line -  0808 808 00 00 7 days a week between 8am-8pm

    Community Champion badge

  • Hi mucus cyst sister!

    The joys of cancer and  it’s side effects. But at least we are still around  to laugh and advise others. 
    Yes we are on the whole well looked after.
    Hazel x

    Hazel aka RadioactiveRaz 35 radiotherapy and 2 chemo  3 rd cancelled. HPV tonsil cancer 7 lymph nodes. 8 years post treatment living a great life. 
    No questions too daft to ask. 

    I’m also an ambassador for https://oraclehnc.org.uk/
    A leading head and neck cancer charity. 

    This is a link to a webinar i did with Oracle explaining the process of diagnosis. 

  • Try saying "mucous cyst sisters" ten times fast! Quality new tongue twister ladies.

    Community Champion Badge

    Metastatic SCC diagnosed 8th October 2013. Modified radical neck dissection November, thirty-five radiotherapy fractions with 2xCisplatin chemo Jan/Feb 2014. Recurrence on larynx diagnosed July 2020 so salvage laryngectomy in September 2020.

    http://mike-o.blogspot.co.uk/

  • Just tried it Mike if I wasn’t dry mouthed before I am now ! But good tongue exercises 
    Hugs Hazel 

    Hazel aka RadioactiveRaz 35 radiotherapy and 2 chemo  3 rd cancelled. HPV tonsil cancer 7 lymph nodes. 8 years post treatment living a great life. 
    No questions too daft to ask. 

    I’m also an ambassador for https://oraclehnc.org.uk/
    A leading head and neck cancer charity. 

    This is a link to a webinar i did with Oracle explaining the process of diagnosis. 

  • Those new scopes are amazing.  I always get a walk though after being scoped as I find it interesting to see bits I can't normally see.

    I have a blocked salivary gland which comes and goes.  Always in the same place - grows, not really sore then decides to disappear.  I raised it with my consultant and he is sure that is what it is, but has offered me a biopsy if I am still concerned.

    The after care I get is really good, especially if you work with your team and let them know of any concerns rather then hiding them and hoping.

    Peter
    See my profile for more details of my convoluted journey
  • Hi Peter. My consultant did a walk through of the video in slow motion with me. Then bless her she allowed  me to do a video and take stills . I did try to upload a photo but medical images aren’t allowed. I have to agree the HD images are fascinating. My cyst hadn’t altered in 3 months so we agreed to leave it 6 months if still the same in her words she will dive in and whip it it. Yes work with your team all the way. 
    Hazel 

    Hazel aka RadioactiveRaz 35 radiotherapy and 2 chemo  3 rd cancelled. HPV tonsil cancer 7 lymph nodes. 8 years post treatment living a great life. 
    No questions too daft to ask. 

    I’m also an ambassador for https://oraclehnc.org.uk/
    A leading head and neck cancer charity. 

    This is a link to a webinar i did with Oracle explaining the process of diagnosis. 

  • Former Member
    Former Member

    Thanks for posting this.  It's reassuring to know that your consultant is keeping a check on the cyst.  Also good to know that these things can occur some time after the initial treatment, so regular checks are very necessary.  Take care and keep us informed x

  • No problem it helps to share information between fellow sufferers. 
    Hazel x

    Hazel aka RadioactiveRaz 35 radiotherapy and 2 chemo  3 rd cancelled. HPV tonsil cancer 7 lymph nodes. 8 years post treatment living a great life. 
    No questions too daft to ask. 

    I’m also an ambassador for https://oraclehnc.org.uk/
    A leading head and neck cancer charity. 

    This is a link to a webinar i did with Oracle explaining the process of diagnosis.