Hemifacial Spasm
Evaluation and treatment planning for hemifacial spasm, a facial nerve disorder causing involuntary twitching or contractions on one side of the face.

Glioblastoma, also called GBM or glioblastoma multiforme, is an aggressive malignant brain tumor and high-grade glioma. It can grow into nearby brain tissue and may affect areas that control speech, movement, vision, memory, balance, behavior, and personality.
In current medical classification, adult glioblastoma is usually described as glioblastoma, IDH-wildtype, CNS WHO grade 4. This means the diagnosis is based not only on how the tumor looks under the microscope, but also on molecular testing. Important markers may include IDH status, MGMT promoter methylation, EGFR amplification, TERT promoter mutation, and chromosome 7 gain/chromosome 10 loss.
De Novo Brain & Spine evaluates patients with suspected or confirmed glioblastoma using neurological examination, brain MRI, and tissue diagnosis when appropriate. Treatment may involve biopsy, image-guided craniotomy, maximal safe brain tumor resection, radiation therapy, temozolomide chemotherapy, tumor treating fields, clinical trials, and coordinated neuro-oncology care.
Glioblastoma symptoms depend on the tumor’s size, location, growth pattern, and swelling around the tumor. Symptoms may develop gradually or appear suddenly.
Common signs and symptoms may include:
Seek emergency medical care or call 911 for a first-time seizure, sudden weakness, sudden speech difficulty, severe confusion, loss of consciousness, or a rapidly worsening headache with vomiting or neurological changes.
Most glioblastomas are sporadic, meaning they develop without a clear inherited cause. In many patients, there is no known preventable reason why the tumor formed.
Possible risk factors may include:
Doctors may also review molecular and genetic tumor features to better classify the glioblastoma and guide treatment planning. These may include IDH-wildtype status, MGMT promoter methylation, EGFR amplification, TERT promoter mutation, and chromosome 7 gain/chromosome 10 loss.
Glioblastoma is not usually caused by a head injury, routine daily activity, or a single lifestyle factor. Diagnosis and treatment decisions depend on imaging, pathology, molecular testing, neurological function, and the patient’s overall health.
Glioblastoma cannot be diagnosed by symptoms alone. Diagnosis usually requires a combination of medical history, neurological examination, brain imaging, and tissue testing.
Common diagnostic steps may include:
These results help the care team understand the tumor type, confirm the diagnosis, plan treatment, and determine whether surgery, radiation, chemotherapy, clinical trials, or other therapies may be appropriate.
Molecular testing examines certain biological features of tumor tissue. These findings provide information beyond what can be seen on a brain scan or under a microscope alone.
Healthcare professionals may consider molecular results together with pathology, imaging, neurological findings, and medical history to develop a more complete understanding of the tumor. The specific tests performed can vary depending on the individual case and available tissue.
Glioblastoma treatment is individualized. The right plan depends on the tumor’s size, location, molecular profile, symptoms, neurological examination, surgical risk, age, overall health, and goals of care.
Treatment options may include:
Surgery is not appropriate for every patient with glioblastoma. When surgery is considered, the goal is usually to obtain a diagnosis, reduce tumor burden, relieve pressure on the brain, and preserve neurological function as safely as possible.
Glioblastoma is one specific type of primary brain tumor, meaning it starts in the brain itself rather than spreading there from another part of the body. Not every brain tumor is glioblastoma. Tumors that spread to the brain from cancer elsewhere in the body are called metastatic brain tumors, and they are evaluated and treated differently even though some symptoms can look similar.
Not always. Some patients undergo image-guided surgery to remove as much of the tumor as safely possible, while others have a biopsy first if the tumor’s location makes full removal higher risk. The right approach depends on the tumor’s size, location, and the patient’s neurological exam and overall health, which is why evaluation comes before any treatment decision.
After diagnosis, care usually involves a coordinated team that may include neurosurgery, radiation oncology, and neuro-oncology, working together on a treatment plan specific to the tumor’s molecular features and the patient’s health. This is typically when decisions about surgery, radiation, chemotherapy, or clinical trial options are discussed.
Yes. A second opinion can help confirm a diagnosis, review imaging and pathology findings, or discuss treatment options before moving forward. Many patients and families find this a helpful step when facing a new brain tumor diagnosis.

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Evaluation and treatment planning for hemifacial spasm, a facial nerve disorder causing involuntary twitching or contractions on one side of the face.
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