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Transverse Myelitis Association
Volume 5 Issue 1
December 2002
Page 11
Gevallestudie: Transvers Miëlitis
Alet Uys’ Case Study as Published by Geneeskunde/The Medicine Journal, South
Africa
Alet Uys has TM and is a member of the TMA. She is a 13 year old living
in Pretoria South Africa. Alet has conducted research and wrote a case
study which has been published by MedPharm’s journal, The Medical Journal.
Douw Greeff, MD, the Managing Editor of Geneeskunde/The Medicine Journal,
has granted us permission to publish Alet’s paper about TM. According
to Dr. Greeff, Alet is the youngest person to ever publish in The Medical
Journal.
Alet’s research and paper were exhibited at the Gauteng Provincial Exposition.
She received a gold medal for her work and received an invitation to participate
in the National Science Exposition. She also received a certificate
of achievement from The Centre for Schools of Quality AFRICA for excellence
in Medical Research. The Centre has trustees in the United States,
Turkey, China and South Africa. Alet has received the AVENTIS First
Prize, for outstanding achievement in medical science.
No less than seven doctors in various branches of medicine visited her stand
during the Gauteng Provincial Exposition. The doctors asked her many
questions about her research and paper. She dealt with the learned
men in a very calm and confident manner, as she was so sure of her facts.
The National Exposition, held in October 2002, is a Youth Science Competition
and the most prestigious competition of its kind in Africa. No less
than 400 schools participated in the Provincial Exposition; whilst 450 schools
participated with 700 projects at the National Exposition. Alet received
the gold medal at the National Exposition for the best project in the category,
“primary school medical sciences.” Alet will have the opportunity to
exhibit her project in Moscow next year.
Alet’s ultimate goal is to go to medical school and to become a neurologist.
Alet Uys's article has been published in Afrikaans in the 2002 July issue
of Geneeskunde/The Medicine Journal: Uys A. Transverse Myelitis. Case Study.
(Afr) Geneeskunde 2002;43(July)(6):47-50 (ISSN 0016-643X) The article
is also available on the Geneeskunde/The Medicine Journal website www.medpharm.co.za.
The following article is a direct translation of the Afrikaans article as
published.
I am a 13 year old, grade seven pupil and currently headgirl at Lynnwood
Primary school (an Afrikaans school in Pretoria, South Africa). My experience
with Transverse myelitis at the age of 11 motivated me to do research on
this topic for our school’s grade 6 and 7 science expo.
My goal with this research is to improve awareness about Transverse myelitis,
especially among medical students and qualified doctors, as the disease is
very rare, information in medical literature does not always provide all
the answers and the disease can only be cured if it is diagnosed and treated
very early.
Two thirds of all Transverse myelitis sufferers do not recover completely;
I am very fortunate and grateful to be one of the patients in the world who
recovered completely from this disease because of early diagnosis.
My research is a way through which I also want to reflect my appreciation
for regaining my health.
My work is dedicated to dr Joe Terblanche (Neurologist at
Unitas hospital, Centurion, South Africa) who helped me and motivated me
to progress, step by step, to where I am today.
My experience with Transverse myelitis started on 2 October 2000. I felt
pain from deep within my upper legs and the sensation of a tight band around
my waist. The constant and terrible pain kept me awake at night and I felt
very sick.
Tuesday October 03: I went to see my family doctor. He drew some blood and
suggested that my condition was caused by growing pains. When we phoned him
the following day for the results, we were told that the blood got ‘lost’
and again the doctor said that my condition was only caused by growing pains.
Thursday October 05: My parents decided to take me to an orthopedic surgeon
who confirmed that my condition was probably due to ‘growing pains’ and he
prescribed Voltaren gel, which he believed would help to relieve the pain.
I was also told to go for an isotope scan the following day in order to confirm
the diagnosis.
Friday October 06: The Voltaren gel did not relieve my pain. I went for the
isotope scan and the results indicated that everything was fine.
My parents and I found it hard to believe that growing pains could be so
constant and bad, causing me to wake up time and again during the night.
Sunday evening October 08: I fell out of bed when I tried to get up
to go to the bathroom. My parents phoned the orthopedic surgeon at his home
and informed him about the weakening condition of my legs. We were
told to visit his rooms the following day; when he realized that my problem
was not of an orthopedic nature, but neurological, I was immediately referred
to a neurologist for a complete neurological examination.
Monday morning October 09: I was finally admitted to hospital with the diagnosis
of acute Transverse myelitis and accompanying minor bladder complaints.
Transverse myelitis is a very rare neurological disease that affects
one out of a million people each year. The patient’s autoimmune system mistakes
the myelin sheath of the spinal cord for intruders and attack the sheaths,
causing inflammation of the spinal cord.
Autoimmune diseases are the result of antibodies or T cells that attack molecules,
cells, or tissues of the organism that produce them; the following process
occurs:
When a germ enters a person’s bloodstream, white blood cells are activated
to arrest (via phagocytosis) and transport the germ to the closest lymph
node. The lymph node then produces T cells and antibodies to attack
and destroy the germ. The antibodies attack the person’s tissues by
mistake, because certain proteins of the person’s tissues resemble the protein
covers of the germ.
In the case of Transverse myelitis, the antibodies attack the nerve tissues
located in the person’s spinal cord. The person’s own antibodies become
a greater danger than the original germ itself, because the antibodies do
not only attack and destroy the original germ, but also the person’s own
tissues (spinal cord nerves). Messages between central and peripheral
nerves are interrupted because of myelin damage caused by the antibodies
and the person becomes sick. The condition may deteriorate and progress to
paralysis if the disease is not treated promptly, because the antibodies
will damage the nerve cells permanently and the person will lose complete
function of the bodily areas supplied by these nerves e.g., loss of function
of legs and bladder.
Speedy and timely administration of high intravenous doses of cortisone decrease
inflammation and swelling of the spinal cord by suppressing the patient’s
immune response, providing the possibility of less structural tissue damage
incurred to nerve cells and a greater chance for recovery.
Autoimmune disease in itself is not rare; Multiple sclerosis, rheumatoid
arthritis, SLE, rheumatic fever and nephritis in children are all examples
of autoimmune diseases. Transverse myelitis is however a rare way in which
autoimmune disease presents. In this instance the antibodies specifically
attack the spinal cord tissues.
The myelin sheaths of the nerves become damaged or destroyed at the point
of inflammation. This prevents communication between peripheral and central
nerves, causing various degrees of motoric and sensoric dysfunction.
Characteristically, the clinical picture presents on both sides of the body,
below the spinal cord area affected by the disease. This occurs because the
disease process involves the complete width of the spinal cord.
Transverse myelitis may be acute or sub-acute. During
an acute attack, the disease develops over a period of a few hours or days.
The clinical picture of a sub-acute attack may develop over a period of 1
to 2 weeks.
Early symptoms may include sudden low back pain, loss of muscle power, paresthesia
in the toes and feet (within the first few hours up to several weeks), pain
in the legs and sensoric loss with partial or total motoric paralysis. Loss
of sphincter function may also occur (loss of bladder control is common).
Other symptoms and signs include muscle spasms, poor appetite, headache,
fever, a general feeling of discomfort and hyperesthesia during changing
weather conditions. Some patients may also experience respiratory problems,
depending on the level of spinal cord damage.
Most people only experience one episode of Transverse myelitis in a lifetime.
Children and adults, both male and female, may present with Transverse
myelitis. At present, there is no proof of any hereditary predisposition.
All races and families are therefore vulnerable. The highest incidence is
found amongst age groups 10 to 19 and 30 to 39 years.
The four classic characteristics of Transverse myelitis are
- Varying degrees of motoric loss in arms and legs
- Pain (the most prominent symptom), especially in the lower
back, as well as sharp shooting pains in the leg
- Sensoric changes
- Loss of bladder control
Most patients experience various degrees of weakness in their legs. Patients
may stumble or drag one foot when they try to walk. They may also experience
a sensation where one or both legs feel heavier than normal. Total
motoric paralysis may follow as the disease progresses, confining the patient
to a wheelchair.
Although some patients recover completely, the majority suffer permanent
damage to their spinal cords, causing considerable morbidity in their daily
lives.
The extent of pathological dysfunction to areas of the body relates directly
to the level of the segment affected in the spinal cord.
The results of my tests indicated that I had an absolute motoric
level at T10 and a strength grading of 1/5 in my left leg and 2/5 in my right
leg. Other tests included a MRI scan and later that week a Lumbar puncture.
Both investigations were indicative of problems.
The diagnosis for Transverse myelitis is reached by obtaining a complete
medical history and performing a complete neurological examination.
Special investigations that are valuable in assisting to make the diagnosis
include, MRI (magnetic resonance imaging) scan of the spinal cord; Myelography
(contrast medium is injected into the subarachnoid space and X-rays are then
obtained); Hematological (blood) tests for HIV status and vitamin B12 levels;
CSF (cerebrospinal fluid) analysis to exclude high protein levels and a high
white cell count.
Spinal cord injuries caused by trauma, tumors or abscesses and shortages
of vitamin B12 need to be excluded as possible causes for the symptoms.
Idiopathic Transverse myelitis is diagnosed when no specific cause
can be identified.
I was started on treatment with Soli-Medrol, 500mg per day for 5 days, and
my condition improved dramatically.
The treatment focus is mainly geared towards providing the patient with symptomatic
relief (the degree of neurological dysfunction may have an effect on the
severity of symptoms experienced by the patient); Treatment includes
- Corticosteroid therapy, which is the primary form of treatment
during the first weeks of the disease. It decreases inflammation and swelling
of the spinal cord and it also suppresses the patient’s immune response,
but it does not alter the course of the disease
- Relief of pain, on an ‘as needed’ basis
- Bed rest during the initial phase of the disease
- The monitoring of vital signs, especially in patients with
respiratory problems
- Expectant observation
- A multi-disciplinary approach by a team consisting of a
neurologist, specialist physician, hematologist, microbiologist and nursing
staff
- Physiotherapy, which plays a very important role during
the recovery phase, should focus on strengthening of muscles and improvement
of coordination and general movement.
After my treatment, I received physiotherapy for about 2 months.
I had to learn to walk again and had to do exercises to develop and regain
my balance and strength. The sensation in my body and limbs also started
to return and I made very good progress.
Sunday, October 15: The cortisone treatment was stopped and that morning,
the same pain of the previous week returned. I was re-admitted to hospital
at about 7am and treated with a three-day course of cortisone.
At this stage the doctor decided to start treatment for Bilharzia (a chronic
condition that I was diagnosed with during all the special investigations
that occurred) for which I received Biltricide, 1200mg once that evening
and 600mg the following morning.
October 19: I felt healthy in general and was discharged from hospital. I
continued treatment with Prednisone 60mg per day for four days, which was
reduced by 5mg every day thereafter, Slow K 1 to 2 times per day, Calcium
Sandoz 1 per day and Losec.
The neurologist explained that my autoimmune system over-reacted against
another type of infection or virus, and attacked my own spinal cord. No other
causes could be found. Because of all this I could not attend the last quarter
of school or write my exams.
At present there is little known about the possible etiological factors that
may cause Transverse myelitits to occur. The condition mostly results after
viral infections, followed by an abnormal immune reaction or it may also
occur as a result of insufficient blood supply to certain segments of the
spinal cord. Infective agents that may play a role include chicken-pox (Varicella),
shingles (Herpes simplex), flu virus, rubella (German measles) Hepatitis
A and rubeola (Measles). Other causes may include bacterial infections of
the skin, middle ear and respiratory tract.
It may also occur as a complication of vaccination against e.g., rabies or
chicken-pox.
When Transverse myelitis follows an infection, the secondary immune
response causes more damage to the spinal cord than the primary viral or
bacterial infection. The secondary immune response (autoimmune reaction)
is considered to be the main cause of the symptoms, resulting in the clinical
picture of Transverse myelitis.
Recovery from Transverse myelitis starts within 2 to 12 weeks after
the onset of the disease. It may however prevail for up to two years. It
is very unlikely that a patient will recover if there is no improvement within
the first 3 to 6 months. One third of patients with Transverse myelitis
recover completely or partially i.e., they can walk again and are able to
maintain bladder control. Another third show moderate recovery with permanent
areas of sensoric deficit on the skin, have problems with bladder control
and present with spastic movements. The last third do not recover and remain
paralyzed and confined to a wheelchair.
Early diagnosis and treatment with corticosteroids mean less damage to the
myelin, an improved prognosis and a better chance of recovery.
It is my wish that more people in the medical profession (especially family
doctors) will in future be able to recognize Transverse myelitis in its early
stages so that the patient can be referred to a neurologist as soon as possible
for immediate treatment.
I would like to thank
Dr Joe Terblanche (Neurologist)
Dr Izelle Smuts (Pediatric Neurologist)
Dr Andre Nel (Prometheus Healthcare)
Prof. Suzanne Delport (Pediatrician)
Dr Douw Greeff (Editor : Medical Science)
Mr At Meyer (Menlopark Science Academy)
Me Saartjie Roos (Science teacher, Lynnwood Primary School)
Alet Uys (13)
Headgirl 2002, Lynnwood Primary School
Web links :
Google.com TRANSVERSE MYELITIS FACT SHEET
www.paralysis.org
www.spinalvictory.org
www.themiamiproject.org
www.myelitis.org
www.naric.com
Areas of research include :
- To determine the role of the immune system in the destruction
of myelin
- The development of strategies to facilitate the regeneration
and repair of damaged myelin
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