What Is Tumefactive Multiple Sclerosis?
Source: Genetic and Rare Diseases (GARD) Information Center
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Tumefactive Multiple Sclerosis
Diffuse cerebral sclerosis of Schilder; Concentric demyelination; Balo's concentric sclerosis; Marburg variant; Balo disease; Baló concentric sclerosis; Balo's disease
Tumefactive multiple sclerosis is characterized by a tumor-like lesion larger than two centimeters and signs and symptoms similar to those of a brain tumor. It is a rare form of multiple sclerosis (MS).
Meninges - Protective Layer of Brain and Spinal Cord
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Source: Genetic and Rare Diseases (GARD) Information Center
Muscle, Bone and Nervous System
Image by TheVisualMD
Multiple sclerosis (MS) is a nervous system disease that affects your brain and spinal cord. It damages the myelin sheath, the material that surrounds and protects your nerve cells. This damage slows down or blocks messages between your brain and your body, leading to the symptoms of MS. They can include
No one knows what causes MS. It may be an autoimmune disease, which happens when your immune system attacks healthy cells in your body by mistake. Multiple sclerosis affects women more than men. It often begins between the ages of 20 and 40. Usually, the disease is mild, but some people lose the ability to write, speak, or walk.
There is no single test for MS. Doctors use a medical history, physical exam, neurological exam, MRI, and other tests to diagnose it. There is no cure for MS, but medicines may slow it down and help control symptoms. Physical and occupational therapy may also help.
Source: NIH: National Institute of Neurological Disorders and Stroke
Studies suggest that there are many factors that influence whether a person will develop multiplesclerosis (MS). The factors that contribute to its onset are multiple and may vary from person to person. The signs and symptoms of MS occur as a result of inflammation, loss of the protective nerve covering (myelin), and the breakdown of nerve cells.
The most widely accepted theory is that MSbegins as an autoimmune disorder, where white blood cells (lymphocytes) attack healthy tissues. Later, signs and symptoms occur as a result ofabnormal activity of specific cells in the brain and spinal cord(microglial cells) and progressive injury and loss of brain and spinalcord cells.
Additional theories regarding the cause of MS include chronic viral infections and genetic disease. Although many viruses, and particularly the Epstein-Barr virus, have been associated with MS, there is no specific evidence linking viruses directly to the development of MS. Still, Epstein-Barr virus infection is considered a risk factor for the disease. Certain gene changes, including onesin HLA-DRB1 are associated with an increased risk for developingmultiple sclerosis. However, it is unclear exactly what role thesegene changes play in the development of MS. Having a first-degree relative with MS, like a parent or sibling, does increase a persons risk for the condition (to around 2%). Learn more about gene changes and MS.
Vitamin D is another area ofinterest. Those who are exposed to more sunlight tend to have higherlevels of naturally-produced vitamin D, which is thought to support theimmune function and may help protect against immune-mediated diseaseslike MS.
Source: Genetic and Rare Diseases (GARD) Information Center
Symptoms of multiple sclerosis (MS) may be similar to those of many other nervous system disorders. The disease is made based on the person's signs and symptoms and is typically diagnosed by ruling out other conditions.
"Dissemination in time and space" are commonly-used criteria for diagnosing the relapsing-remitting form of MS (RR-MS). "Dissemination in time means" that there are at least two clinical attacks, each lasting at least 24 hours, separated by at least one month, or a slow, step-wise progressive course for at least six months. "Dissemination in space" means that there are lesions in more than one area of the brain or spinal cord. For primary progressive MS (PP-MS), there are currently no diagnostic criteria that are universally accepted.
Physicians may do many tests to evaluate an individual suspected of having MS.
The Revised McDonald Criteria, published In 2010 by the International Panel on the Diagnosis of Multiple Sclerosis, include specific guidelines for using MRI, visual evoked potentials (VEP) and cerebrospinal fluid analysis to speed the diagnostic process.
Source: Genetic and Rare Diseases (GARD) Information Center
Source: Genetic and Rare Diseases (GARD) Information Center
Source: Genetic and Rare Diseases (GARD) Information Center
Axon and Myelin Sheath
Image by TheVisualMD
Schilder's disease is a rare progressive demyelinating disorder which usually begins in childhood. Schilder's disease is not the same as Addison-Schilder disease (adrenoleukodystrophy). Symptoms may include dementia, aphasia, seizures, personality changes, poor attention, tremors, balance instability, incontinence, muscle weakness, headache, vomiting, and vision and speech impairment. The disorder is a variant of multiple sclerosis.
Treatment for the disorder follows the established standards in multiple sclerosis and includes corticosteroids, beta-interferon or immunosuppressive therapy, and symptomatic treatment.
As with multiple sclerosis, the course and prognosis of Schilder's disease are unpredictable. For some individuals the disorder is progressive with a steady, unremitting course. Others may experience significant improvement and even remission. In some cases, Schilder's disease is fatal.
Source: National Institute of Neurological Disorders and Stroke (NINDS)
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