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The Prayers from Maria Foundation is actively funding research into specific forms of childhood cancer known as gliomas.

What is a Glioma?
A glioma is a cancer of the brain, or brain tumor, which forms in the glial cells of the central nervous system. Glial cells are those that surround and support nerve cells. While some brain cancers originate elsewhere in the body, gliomas originate in the central nervous system, and are often called “primary” brain tumors.

Beyond the location of their origin, gliomas have a number of characteristics. One important characteristic of malignant gliomas is that they do not have clearly discernable boundaries, or are “diffuse.” 1 Even if removed, portions of a glioma often remain and lead to relapse. While gliomas do not spread outside of the central nervous system, it is common to find multiple gliomas throughout the brain stem during relapse phases of the disease.

Gliomas are disproportionately common among children, and they are the second highest cause of cancer death among young people. Different forms of gliomas, however, have different prognoses and treatments. Over 97% of children with the worst of the gliomas, diffuse pontine gliomas, die within three years. 2

Different Types of Gliomas
There are many different forms of gliomas, which are categorized by their location in the brain stem as well as a number of other criteria. It is often difficult, however, to obtain an accurate diagnosis, as many gliomas appear similar yet act differently.

In the future, accurate diagnosis of specific gliomas will likely become more important. Currently, however, the location of the glioma generally dictates the treatment. Gliomas occurring in the midbrain, the dorsum of the medulla, or elsewhere in the brain stem can often be treated through surgical removal (in combination with radiation and chemotherapy), which dramatically increases the chances of survival. Some forms of gliomas, in particular many that arise in the pons or supratentorial hemisphere, cannot be removed surgically, and therefore are treated primarily with radiation and chemotherapy.

According to St. Jude, in such cases “the patients' symptoms often improve dramatically during or after six weeks of irradiation. Unfortunately, problems usually recur after six to nine months, and progress rapidly. Survival past 12 to 14 months is uncommon, and new approaches to treating these tumors are urgently needed.” 3


1 Fisher, P.G. & Buffler, P.A. (2005) “Malignant Gliomas in 2005: Where to GO From Here?” Journal of the American Medical Association, 2005; Vol. 293, No.5.
2 Wagner, S., et al (2006) “Treatment options in childhood pontine gliomas,” Journal of Neuro-Oncology (2006) 79: 281–287.
3 http://www.stjude.org/stjude/v/index.jsp?vgnextoid=b86c061585f70110VgnVCM1000
001e0215acRCRD&vgnextchannel=bc4fbfe82e118010VgnVCM1000000e2015acRCRD


The Symptoms of Gliomas

Symptoms common across multiple forms of gliomas include headaches, seizures, speech or reasoning difficulties, diminished vision, loss of balance, nausea, and physical weakness or paralysis. However, other symptoms arise in line with the location of the glioma. For example, a pontine glioma may involve difficulty swallowing whereas a glioma in the medulla can be associated with weakness in the legs and arms.

For More Information
St. Jude Children’s Hospital
Children’s Memorial Hospital
The Mayo Clinic
The National Cancer Institute

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