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Treatment of Syringomyelia (Myelosyringosis or Spinal gliosis) abroad

Syringomyelia is a medical term meaning presence of a single or multiple cavities in the spinal cord. Slow, but steady progression is peculiar for the disease. The process of the disease can significantly reduce the quality of a patient’s life and sometimes lead to death. Syringomyelia is difficult to treat and most of the existing therapeutic techniques are aimed at easing the symptoms of the illness. 

 

Syringomyelia treatment abroad

 

Causes of syringomyelia

Syringomyelia can be primary or secondary. Secondary form of the illness has a clear relationship between the appearance of the cavities in the spinal cord and an event or pathological process.

 

Syringomyelia can be caused by:

  • Injury
  • Infectious disease of the central nervous system
  • Tumour
  • Spinal hernia
  • Vascular diseases

 

Primary form of the illness doesn’t have any connection between the formation of cavities in the spinal cord and other pathological processes or events.

 

Basic causes of the primary disease are:

  • Defect of nervous tissue in embryonic development
  • Congenital anomalies in the structure of the spine

 

A number of cases have an unclear cause. Then an idiopathic form of syringomyelia is diagnosed.

 

Risk factorsare:

  • Age between 20-40
  • Female sex
  • Physical work
  • Dysgraphic status (short height, non-growth of vertebral arches, disproportionate limbs, asymmetric chest)

 

Syringomyelia symptoms

 

Symptoms of syringomyelia

Syringomyelia is peculiar with sensitive, motor disorders, vegetative and trophic disorders.

 

Sensitive disorder syndrome is the most frequent clinical sign. It develops in all patients suffering with the disease. Usually, the illness starts with the sensory disorder.

 

Possible symptoms are: 

  • Pain in the chest, upper limbs, cervico-brachial region (location corresponds to the areas of innervation of individual spinal nerves)
  • Loss of pain and temperature sensitivity in certain parts of the body
  • Preservation of tactile (pressure) and vibration sensitivity

 

Often, patients are observed to have burns or post-burn scars on their upper-limbs during the objective exam. The reason is due to the absence of temperature sensitivity. 

 

Syndrome of motor disorders appears later, as syringomyelia progresses and this is characteristic for 75% of patients.

 

Main manifestations are: 

  • Decreased muscle volume
  • Decreased muscular strength and endurance
  • Twitching of the muscles
  • Decrease or loss of reflexes
  • Impaired urinary bladder function, up to incontinence

 

Upper-limbs are damaged while lower extremities are rarely affected. In that case, syringomyelia is manifested by the weakness of the legs and their atrophy. The central lower paraparesis may develop (strengthening of muscle tone). A person can simultaneously have signs of central (muscle spasm) and peripheral (lethargic) paralysis.

 

65-70% of patients experience vegetative-trophic disorders that are associated with the damage of the spinal cord lateral horns.

 

Basic symptoms are:

  • Muscles, skin, joints atrophy and reduction of their volume
  • Restricted mobility of the joints
  • Gray hair in the zone of impaired autonomic innervation
  • Hairloss
  • Brittlenails
  • Cracks in the skin, purulent wounds, blue shade of hands, non-healing ulcers

 

30% of patients have their bones damaged as they become weaker. Thus, the risk of a fracture also increases. There may also be an issue of enlarged fingers. 

 

Every third patient has some sort of heart disorder. They experience cardiac pains, signs of arrhythmia (interruptions in the work of the heart, cardiac resignation). Other organs are  rarely affected. There may be a malfunction of the liver, and gastrointestinal tract.

 

Syringomyelia diagnostics

 

Diagnostics of syringomyelia

An illness can be suspected on the basis of:

  • Patient’scomplaints
  • The nature of the clinical course (gradual onset, slow progression)
  • Data from the neurological examination
  • X-raysurveys

 

Diagnostics is based on the methods of neuroimaging. A doctor prescribes the following procedures to confirm a diagnosis:

  • Spondylography (radiologic examination of the vertebrae)
  • Computedtomography
  • MRI
  • Myelography (examination of the cerebrospinal pathways, used when it is impossible to perform CT or MRI for technical reasons)

 

Treatment of syringomyelia abroad

Majority of patients receives conservative treatment only. The goal of treatment is to eliminate the disease symptoms and prevent possible complications. Vascular drugs, cholinesterase inhibitors like Proserin, anesthetics, vitamins are prescribed.

 

Syringomyelia treatment abroad

 

Radiation or radionuclide therapy may be effective at the initial stage of the disease. They are aimed to slow down the progression of syringomyelia. The irradiation of the spinal cord or the introduction of radioactive elements (iodine and phosphorus) into the patient’s body is also used. Courses are held at intervals of six months to several years.

 

Surgical methods cannot cure syringomyelia, but many patients can achieve sustained clinical improvement. Symptoms decrease in most patients. Different surgical approaches are indicated, which depends on the level of damage, the clinical course of the disease and the technical capabilities of the medical institution.

 

Surgeries indicated are aimed at: 

  • Drainage of cavities in the spinal cord
  • Restoration of cerebrospinal fluid
  • Proper circulation
  • Dismemberment of adhesions
  • Decompression of the spinal cord
  • Dissection of the spinal cord end thread

 

The disease is extremely difficult to treat. Therefore, it is better to treat syringomyelia in a reputable European hospital, like the ones found in Germany. Here the latest techniques of syringomyelia treatment are available along with best healthcare and developed health tourism.

 

Syringomyelia prognosis

 

Prognosis for syringomyelia

Life prognosis is favourable for those who suffer form syringomyelia as life expectancy isn’t necessarily reduced. Lethal outcomes are rare and mainly associated to:

  • The transition of the disease to the medulla oblongata and respiratory depression
  • The formation of bedsores with the development of infectious complications, including sepsis
  • Damage of an X-pair of cranial nerves and violation of cardiac activity

 

Work capacity prognosis is not favourable though. Most of the patients become disabled. Life quality considerably decreases because of the chronic pain, motor and vegetative disorders. 

 

 


 

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2312.00
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2833.00
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11903.00
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832.00
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