Acoustic neuroma -what are the signs symptoms and treatments of Acoustic neuroma?

Acoustic neuroma

Acoustic neuroma

An acoustic neuroma is a benign (non-cancerous) growth, or tumour, in the brain. It’s also known as a vestibular schwannoma.

An acoustic neuroma grows on the vestibulocochlear nerve, which helps control hearing and balance. This nerve runs alongside the facial nerve, which carries information from the brain to the face muscles.

The symptoms of an acoustic neuroma tend to develop gradually and can vary in severity. This can make the condition difficult to diagnose (see below).

A small acoustic neuroma can lead to problems with:

  • hearing – causing hearing loss or tinnitus (a noise perceived inside the ear but with no outside source)
  • balance – causing vertigo (the sensation that you’re spinning)

  • A large acoustic neuroma can cause a number of symptoms, including:

    • headaches with blurred vision
    • numbness or pain on one side of the face
    • problems with limb co-ordination on one side of the body

    Occasionally, large neuromas can also result in muscle weakness on one side of the face. In rare cases, it may also cause changes to the voice or difficulty swallowing (dysphagia).

    What causes an acoustic neuroma?

    The cause of most acoustic neuromas is unknown, but a small number of cases (about 5%) are caused by a rare, inherited condition called neurofibromatosis type 2.

    Acoustic neuromas grow from the cells that cover the vestibulocochlear nerve, called Schwann cells.

    Read more about the causes of an acoustic neuroma.

    Diagnosing an acoustic neuroma

    If your GP thinks you have an acoustic neuroma, you’ll be referred to hospital for tests.

    The three types of test you may have are:

    Read more about how an acoustic neuroma is diagnosed.

    Treating an acoustic neuroma

    Acoustic neuromas tend to grow slowly and don’t spread to other parts of the brain.

    They can be so small and grow so slowly that they may not cause any symptoms or problems. In such cases, the acoustic neuroma may just be monitored to avoid risks associated with surgery.

    In rare cases, the tumour can grow large enough to press on the brain. However, most acoustic neuromas can be treated before they reach this stage, either with surgery to remove the tumour or radiotherapy to destroy it.

    Read more about treating an acoustic neuroma.

    Complications of an acoustic neuroma

    Acoustic neuromas aren’t usually life-threatening but the symptoms can be disruptive. For example, the loss of hearing may affect your ability to communicate with others.

    Speak to your GP or specialist if you feel the symptoms are having an impact on your day-to-day life. There may be ways of easing your symptoms, such as using a hearing aid or taking painkilling medication.

    Read more about complications of an acoustic neuroma.

    [Original article on NHS Choices website]

Achalasia – what you need to know but were afraid to ask!

Achalasia is a disorder of the gullet (oesophagus) where it loses the ability to move food along. The valve at the end of the gullet also fails to open and allow food to pass into your stomach.

Achalasia

Achalasia

As a result, food gets stuck in your gullet and is often brought back up.

A ring of muscle called the lower oesophageal (cardiac) sphincter keeps the opening from the gullet to the stomach shut tight to prevent acid reflux (acidic stomach content moving back up into the gullet).

Normally, this muscle relaxes when you swallow to allow the food to pass into your stomach. In achalasia, this muscle does not relax properly and the end of your gullet becomes blocked with food.

Achalasia is an uncommon condition that affects about 6,000 people in Britain. It is sometimes known as cardiospasm.

What are the symptoms?

Symptoms of achalasia may start at any time of life and usually come on gradually.

Most people with achalasia have dysphagia, a condition where they find it difficult and sometimes painful to swallow food. This tends to get worse over a couple of years.


It may cause you to bring back up undigested food shortly after meals and some of the vomited food may have been held up in your gullet for some time.

Bringing up undigested food can lead to choking and coughing fits, chest pain and heartburn.

Occasionally, vomit may dribble out of your mouth and stain the pillow during the night. If it trickles down your windpipe, it can cause repeated chest infections and even pneumonia.

You may experience gradual but significant weight loss.

However, in some people achalasia causes no symptoms and is only discovered when a chest X-ray or other investigation is performed for another reason.

What is the cause?

Achalasia is caused by damage to and loss of the nerves in the gullet wall. The reason for this is unknown, although a viral infection earlier in life may be partly responsible.

Achalasia may also be associated with having an autoimmune condition, where the immune system attacks healthy cells, tissue and organs. One recent study found people with achalasia are significantly more likely to have an autoimmune condition such as Sjogren’s syndrome, lupus or uveitis.

Although achalasia can occur at any age, it is more common in middle-aged or older adults.

There is no evidence to suggest that achalasia is an inherited illness. Women with achalasia can have a normal pregnancy and there’s no reason why their children will not develop normally.

How is it diagnosed?

If your GP thinks you have achalasia, you will be referred to hospital to have some diagnostic tests performed.

Barium swallow

A barium swallow involves drinking a white liquid containing the chemical barium, which allows the gullet to be seen and videoed on an X-ray.

In achalasia, the exit at the lower end of your gullet never opens properly, which causes a delay in barium passing into your stomach.

An ordinary chest X-ray may show a wide gullet.

Endoscopy

A flexible instrument called an endoscope is passed down your throat to allow the doctor to look directly at the lining of your gullet and stomach. Trapped food will be visible.

The endoscope can be passed through the tight muscle at the bottom of your gullet and into your stomach to check there is no other disorder of the stomach.

Read more about having an endoscopy.

Manometry

Manometry measures pressure waves in your gullet. A small plastic tube is passed into your gullet through your mouth or nose and the pressure at different points in your gullet is measured.

In achalasia, there are usually weak or absent contractions of the gullet and sustained high pressure in the muscle at the lower end of the gullet. The high pressure means the muscle does not relax in response to swallowing, causing symptoms of achalasia.

How is it treated?

The aim of treatment is to open the lower oesophageal sphincter muscle so food can pass into the stomach easily. The underlying disease cannot be cured but there are various ways to relieve symptoms which can improve swallowing and eating.

Dilatation (stretching the muscle)

A balloon (about 3-4cm in diameter) is used to stretch and disrupt the muscle fibres of the sphincter muscle at the lower end of your gullet.

This usually improves swallowing but may need to be performed several times or repeated after one or more years. Balloon dilatation does carry the risk of oesophageal rupture which may require emergency surgery.

Surgery

Under general anaesthetic the gullet is accessed through the abdomen (tummy) or, rarely, the chest. The muscle fibres of the lower oesophageal sphincter that fail to relax are divided. This usually leads to a permanent improvement in swallowing.

The operation is now performed by keyhole surgery (laparoscopy) and only requires an overnight stay in hospital.

Recovering from treatment

There are a few things you can do after dilatation or surgery to reduce symptoms:

  • chew your food well
  • take your time eating
  • drink plenty of fluids with your meals
  • always eat food sitting upright
  • use several pillows or raise the head of your bed so that you sleep fairly upright, which prevents stomach acid rising into your gullet through the weakened valve and causing heartburn

If heartburn develops after treatment, consult your GP as medication may be needed to reduce the acid reflux. Sometimes your surgeon may suggest you take this routinely to prevent problems after surgery. Read about treatments for acid reflux.

You should also see your GP if you still have swallowing difficulties or are continuing to lose weight.

It’s normal for chest pain to persist for a while after treatment – drinking cold water often gives relief.

Cancer risk

If the gullet contains a large amount of food that does not pass into the stomach in the normal way, the risk of cancer of the oesophagus (gullet) is slightly increased.

The increased risk is likely to be most significant in long-term untreated achalasia. It’s therefore important to get appropriate treatment for achalasia straight away, even if your symptoms are not bothering you.

According to Cancer Research UK, compared with the general population:

  • men with achalasia have an eight to 16 times higher risk of oesophageal cancer
  • women with achalasia have a 20 times higher risk of one particular type of oesophageal cancer (adenocarcinoma)

However, cancer of the oesophagus is very uncommon and although your risk is slightly increased, it remains highly unlikely.

Myasthenia gravis – What is Myasthenia gravis? What are the signs and symptoms of Myasthenia gravis?

Myasthenia gravis

Myasthenia gravis

Welcome to the latest in our series of informational blog posts which look at various different autoimmune conditions.  Today we are exploring Myasthenia gravis – looking in more detail at the signs, symptoms and treatments of this condition.  To find out more about autoimmune conditions in general please have a look at our previous post on the subject https://patienttalk.org/?p=939.

As always if you are concerned that you have any of the symptoms of Myasthenia gravis  we would advise you to see a healthcare professional as soon as possible.

So what is Myasthenia gravis?

It is an autoimmune condition which affects 1 in 10,000 people in the UK; according to the NHS.  Interestingly it seems to, typically, effect women under 40 years of age and men over 60.

Simply put it is a condition which leads to muscle weakness.  In particular voluntary muscles which control the movement of things like chewing and swallowing as well as the eyelids.  In more serious cases it can affect those muscles used in breathing.

Typical symptoms include:-

Problems with the eyes are often the first noticeable symptom.  This could include double or blurred vision.  Droopy eye lids are also common.

Dysphagia or difficulty swallowing.  This often leads to slurred speech.  Again a common symptom.

Breathing difficulties in bed or when exercising.

A myasthenia crisis can occur because of swallowing or breathing issues and leads to hospitalisation

Movement issues such as difficulty walking or a drooping head.  This makes physical labour harder for the patient.

Myasthenia gravis occurs because  the body’s immune system creates proteins which attach the muscle receptors.

Treatments typically consist of immunosuppressants and if symptoms persist a steroid treatment may be employed.  In a few rare cases, where the patient is over 60, it may be considered necessary to remove the thymus gland in an operation called a Thymectomy.  This operation can help the immune system rebalance itself.  Where problems with swallowing have become very serious then intravenous immunoglobulin therapy could be applied in a hospital setting.

Do you have Myasthenia gravis?  If so we would love it if you could tell your story.  Please use the comments section below to share anything you think will be of interest.  In particular please could you think about the following questions:-

1)      What were your first symptoms of Myasthenia gravis?

2)      How were you diagnosed?  How long did it take and were any other conditions ruled out?

3)      What treatments have you received and who effective were they?

4)      What was the effect of Myasthenia gravis on your lifestyle?

5)      What one piece of advice would you give to somebody who has just been diagnosed with Myasthenia gravis?

Many thanks in advance for all your help!

 

LyneneLGros I was 2 1/2 yrs old when i was diagnosed. Im 41 and have never lived with this disease. My mother was told i would die at 15. Im a walking and seeing miracle! God has healed me. Ill always owe him my life for giving me life.
mamajanie In my hubs case eye issue was in 2010…drooping lid double vision…dr. visit yeilded a prism in lens….over the years weakness…started c-pap june 2013 with developing jaw issues, and throat, allergies…ent dr. Found nothing…heart lung Dr. Foynd nothing…fell 2-3 times…neuroligist diag. Mg sep. 2013…intensive care un oct….ivig caused severe kudney failure…now on dialysus…mestinon helped tempirarily..steroids cause bad side effects…high blood sugar

International Ataxia Awareness Day. Find out about the symptoms of Ataxia. Please share our Ataxia Awareness graphic!

Today is International Ataxia Awareness Day. It takes place annually on 25th September.

Ataxia is used to describe a number of neurological disorders which impact upon  co-ordination, balance and speech.  It is for example a very common symptom on Multiple Sclerosis.

It can be result from damage to a part of the brain called the cerebellum as well as other parts of the nervous system.

The symptoms of ataxia include:

  • Problems with walking.
  • Balancing difficulties.
  • Difficulty in speaking.
  • Harder to see properly.
  • It can be hard to swallow. Also called Dysphagia.

To find out more about International Ataxia Awareness Day please check out  the International Ataxia Awareness Day page at http://www.ataxia.org/events/international-ataxia-awareness-day.aspx

We have produced an International Ataxia Awareness Day graphic below.  It would be great if you could share this today to help us raise awareness of Ataxia.

International Ataxia Awareness Day

International Ataxia Awareness Day