• The teenager had surgery to remove the growth
  • Extensive facial reconstructive surgery has left 19-year-old with slight disfigurement to her nose

By Chris Parsons

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When Tasha Jilka began suffering from a watery left eye, she put the strange symptom down to her make-up or the seasonal weather.

But far from being an innocuous allergic reaction to cosmetics, the teenager's bizarre ailment was one which changed her life forever, as she was later diagnosed with cancer.

The 19-year-old's watery eye was caused by a rare cancer tumour called olfactory neuroblastoma at the back of her nose which left doctors eventually having to rebuild her whole face.

Rebuilding her life: Tasha Jilka has had extensive surgery to rebuild her face following the shock discovery of a cancer tumour behind her nose

Rebuilding her life: Tasha Jilka has had extensive surgery to rebuild her face following the shock discovery of a cancer tumour behind her nose

Tasha's rare diagnosis was eventually made a year after she first suffered the watery eye, having been missed by doctors and opticians.

Her ordeal began in May 2008, when, aged 16, her symptoms began.

WHAT IS OLFACTORY NEUROBLASTOMA?

Also known as esthesioneuroblastoma, it is a very rare, malignant tumour that develops in the nose.

The tumors are believed to start in the olfactory nerve, which transmits impulses related to smell from the nose to the brain. 

Tumours can be slow-growing or aggressive. The condition is not thought to be inherited and the cause is unknown.

Common symptoms include a nasal obstruction, changes in sesnse of smell, facial pain, watery eyes and changes in vision.

Around 1,200 cases have been diagnosed since the condition was first identified in 1924. It appears to affect both genders and all races equally.

Treatments include surgery, radiation therapy, and possibly chemotherapy.

Five year survival following treatment ranges from 40 to 80 per cent, depending on the stage and grade of the tumour.

Source: hopkinsmedicine.org

Tasha, from Leicester, said: 'My left eye was very watery but I just put it down to make-up. It kept getting worse and I decided to go to my GP.

'It was put down to a cold and the weather and I was told it would go by itself.

'I went back a few times when it didn't get better and was referred to an optician, but they couldn't find anything either.'

Four months later, her eye had got worse and she was referred to a Cambridgeshire hospital, as she was living near there at the time.

Tasha had an operation to clear a blocked tear duct - but it still did not solve her problems.

In 2009, when she and her family moved to Leicester, she again went to her doctor and was referred to specialists at Leicester Royal Infirmary.

Tasha said: 'I had a similar eye test but this time doctors also looked up my nose and could see a lump.'

A biopsy was taken and a short time later, Tasha's cancer was diagnosed.

She said: 'When I was told it was as if they were talking about someone else. I knew it was serious.

'I thought it was a little lump in my face but the news began to sink in.'

In May 2010 Tasha had surgery to remove the tumour.

It was so severe that surgeons had to reconstruct her nose and she is still having problems with the vision in one eye.

Rare: Olfactory neuroblastoma is a form of cancer which affects the superior recess of the nasal cavity (stock picture)

Rare: Olfactory neuroblastoma is a form of cancer which affects the superior recess of the nasal cavity (stock picture)

She has had two major operations, one to remove the tumour and a second to rebuild her nose.

It has also meant the shape of her face has changed.

Tasha said: 'I am very strong and I am pulling through, but it is very hard.

'I feel if I had been diagnosed earlier and known more about the symptoms, I might not have had to have two such major operations.

'I have lost a lot of feeling in my face and my sense of smell.'

Tasha is now backing a campaign by charity the Teenage Cancer Trust to raise awareness of cancer in young people.

Here's what other readers have said. Why not add your thoughts, or debate this issue live on our message boards.

The comments below have been moderated in advance.

It's scary that so many practitioners missed diagnosed the situation in the first place. It pays to be vigilant with your own health and if you feel something isn't right then be a pest if that's what it takes. I know from experience the problems when doctors misdiagnose. My situation resulted in a ruptured appendix and two weeks on a drip.

I also often wonder why so many people are misdiagnosed especially by GP's a lot of whom seem to fob people off by putting everything down to a minor ailment which will right itself. Most people have an inkling when something is really not right with their bodies & I've heard too many stories of GP's not taking people seriously. She's a beautiful girl & so very brave, well done for helping to raise awareness of this disease.

Still pretty. Wish her all the best.

Scary MRI, regretfully it took a while to get the scan done.There wouldn't have been any confusion about the diagnosis. Best wishes for her health and well being. Teenage Cancer Trust is a wonderful thing. Teens with cancer do not have the same needs as small children or older adults. We don't have this in USA yet. I think Roger Daltry is trying to get a Center at UCLA.

What a beautiful girl, take not all the towie crew, all slapped up in your make up, this girls looks amazing

All the ordeal and all the hospital had to do prior to the tear duct surgery was to do an MRI!!! Poor girl.

I'm glad it was caught in time and I wish her the best.

She is so beautiful...... After all this she still appears calm and relaxed.... She must be a beautiful person from within too....

Hope she's okay

I am sorry to say Chris from Herts, you are probably right. No profit for big pharma because they can't patent it. Vitamin C and B 17 are big players too. "let food be your medicine, and medicine be your food" Can't remember who said it!! I don't know what happened to "first do no harm! "

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