Tumefactive multiple sclerosis (MS), also known as Balo’s concentric sclerosis or Balo’s disease, is a rare form of MS with symptoms resembling those of a brain tumor. According to an article in the Journal of Chiropractic Medicine, less than 1 percent of all MS cases are diagnosed as tumefactive MS.
Tumefactive MS typically appears as one or more large brain masses, or lesions, in imaging studies. Such symptoms are not associated with other forms of MS. For this reason, tumefactive MS is frequently misdiagnosed. As with many rare diseases, the direct cause of tumefactive MS is not known or understood.
Tumefactive MS symptoms are very different from the most common forms of MS. Typical MS symptoms include:
Additional physical symptoms of tumefactive MS can include:
Moreover, people with tumefactive MS may experience cognitive impairments including:
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Tumefactive MS is diagnosed in several ways. A doctor will first order a medical history and a neurological exam. Additional tests may then be performed to detect unusual growths; damage to the brain, nerve, spinal cord, or brain stem; or the presence of inflammatory diseases or infections. These tests can also rule out other conditions.
These tests may include:
Because people with tumefactive MS present with atypical symptoms, it’s often misdiagnosed as other conditions including:
For this reason, people with tumefactive MS may be repeatedly misdiagnosed, leading to a delay in treatment.
There are several key differences between tumefactive MS and other forms of MS:
Unlike other forms of MS, tumefactive MS generally progresses rapidly. Disease progression can occur in several ways:
Most cases of tumefactive MS develop into relapsing-remitting MS (RRMS). RRMS is the most common form of MS, affecting about 80 percent to 85 percent of people with the disease.
According to the National Multiple Sclerosis Society, tumefactive MS can worsen over time and lead to severe disability, both physical and cognitive. Not every case of tumefactive MS results in severe disabilities. Some people have reported spontaneous remission of tumefactive MS without the presence of any symptoms.
The cause of tumefactive MS is not known. However, the disease has attributes that may point to other contributing factors.
Case reports show that tumefactive MS brain masses sometimes cause what’s called mass effect, which occurs when the masses affect multiple surrounding brain regions simultaneously. Mass effect is likely responsible for many tumefactive MS symptoms.
Because tumefactive MS is considered an inflammatory demyelinating disease, some scientists theorize that its cause may be rooted in autoimmune disorders.
As with other forms of MS, there’s no single progression path. A variety of treatments can help people with tumefactive MS manage symptoms and slow the progression of the illness. Medications can be taken orally, via injections, or administered intravenously.
Corticosteroids are commonly used in tumefactive MS to decrease the severity of inflammation in affected regions of the brain or spinal cord. This form of MS responds particularly well to corticosteroids.
Therapeutic plasma exchange is commonly used to alleviate certain blood, neurological, or autoimmune disorders. Some diseases can result in an abnormal substance in the blood. Therapeutic plasma exchange replaces damaged plasma with plasma free of abnormalities, which can help slow the disease’s progression and relieve symptoms.
Intravenous immunoglobulin is used as a third-line treatment for different forms of MS. This therapy entails injecting a mixture of antibodies into a muscle, a vein, or under the skin, which helps people with immunodeficiencies fight off a large variety of infections.
Rehabilitation can help those with physical ailments from tumefactive MS to manage weakness or imbalance. Physical, speech, or occupational therapy may be especially helpful.
Lifestyle changes, such as daily exercise, movement routines, or relaxation techniques such as yoga and meditation may help reduce symptom severity.
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I was diagnosed with Tumefactive MS in July 2024. I lost my peripheral vision due to a lesion on my brain. My neuro treated it with Mavenclad. I’m fatigued most days as the drug killed most of my… read more
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