Diseases and Conditions
Epilepsy from any cause, is likely an excellent reason for epilepsy surgery. We care for all patients with the following:
Tuberous sclerosis complex is a genetic condition that causes the development of small non-cancerous growths (tubers) in the brain. Most children with this condition will begin experiencing spasms or seizures during their first year. For at least half of these children, medications alone will not be enough to control the seizures. Ketogenic diets and vagal nerve stimulation may also help.
Surgery may be an option if the seizures can be traced to one or more of the tubers. Removing the tubers, along with some surrounding tissue, can be an effective way to permanently stop the seizures. Fortunately, imaging advances are increasing our ability to identify and pinpoint the troublesome tubers.
Focal cortical dysplasia affects the outermost layer (known as the cerebral cortex) of your child’s brain. This is the area of the brain that controls movement, thoughts, speech, memory, intelligence and personality. The genetic condition causes abnormal groups of cells, or lesions, to form. The resulting seizures often do not respond to medications, making them the most common reason for epilepsy surgery.
Effective surgical treatment requires the most advanced imaging techniques available to accurately map the area of the brain affected by the dysplasia. Younger children and infants are more likely to require more extensive surgeries because their abnormalities (cortical dysplasia type II) tend to be more extensive. Surgery provides a permanent fix for seizures in at least 60 percent of children. Your child may also experience improvements in behavior, attention, development and cognitive skills.
Hemimegalencephaly is a rare genetic condition that causes half of your child’s brain to be abnormally large. It can cause malformations in parts of the brain, which can lead to seizures. These seizures are rarely able to be controlled through medication and can create significant developmental delays if not treated.
For many children, surgery is the best option. This highly specialized treatment disconnects the affected brain hemisphere. The disconnected hemisphere may be left in the skull or removed, depending on the severity of the condition.
Rasmussen’s encephalitis is a very rare brain condition that causes inflammation (encephalitis) in half of your child’s brain. This inflammation grows worse over time, causing frequent seizures that can leave permanent brain damage. It can lead to paralysis, loss of sensation, weakness on one side of the body and mental decline. It most often shows up in children between the ages of 4 and 12 years.
These seizures do not typically respond to medication. Instead, controlling the seizures often requires surgery to disconnect or remove the inflamed brain hemisphere.
Lennox Gustom Syndrome (LGS) is a rare and severe form of epilepsy that typically develops in early childhood and is characterized by multiple types of seizures that can be difficult to control. Children with LGS may also experience developmental delays, learning difficulties and challenges with behavior. Although seizures can be challenging to manage, treatment options such as medications, dietary therapies and epilepsy surgery may help reduce seizure frequency and improve quality of life.
Post traumatic epilepsy is a type of epilepsy that can develop after a child experiences a traumatic brain injury. Seizures may occur weeks, months or even years after the injury and can vary in type and severity. Treatment may include anti-seizure medications, dietary therapies or epilepsy surgery, depending on the child’s seizures and individual needs.
Sturge-Weber syndrome (SWS) is a rare genetic vascular disorder that causes blood vessels to grow abnormally in your child’s brain, skin and eyes. The most visible characteristic is a port wine stain birthmark on the upper portion of one side of your child’s face. This skin lesion is usually there at birth but can change in size and appearance as your child grows.
Birthmarks are far more common than Sturge-Weber. So having a similar birthmark does not mean your child will experience any additional symptoms. But for some children, the vascular disorder can cause malformations in blood vessels in the brain, which can lead to seizures and vision issues. Seizures are often controlled through medication, but surgery may be suggested for children whose seizures do not respond well to medication.
Epilepsy Surgery FAQs
Epilepsy is a fairly common disorder that sparks abnormal electrical surges in your child’s brain, creating seizures. Not all seizures indicate epilepsy. A diagnosis usually follows two or more seizures that were not provoked by other events.
Epileptic seizures can be controlled with medication. Epilepsy is considered “drug resistant” if seizures continue even after your child has tried at least two different anti-seizure medications.
Yes. If seizures aren’t controlled, they can impact your child’s development, including learning and emotional well-being. A seizing brain isn’t a developing brain.
Epilepsy surgery comes in several forms, but they have the same goal: To eliminate or reduce seizures by modifying, disconnecting or removing the part of the brain that is causing them.
At Orlando Health Children’s Neurosurgery Institute, we perform every type of pediatric epileptic surgery available, some of which include:
- Resection or laser ablation is used to target abnormal brain tissue responsible for the seizures.
- Hemispherotomy is a procedure that disconnects the troublesome brain hemisphere from the rest of the brain.
- Corpus callosotomy is used to partially disconnect the brain’s hemispheres. This can help with seizures (drop attacks) that cause your child to fall to the ground.
- Implanted neuromodulation devices can help regulate electrical activity in your child’s brain. These include responsive neurostimulation (RNS), deep brain stimulation (DBS) and vagus nerve stimulation (VNS).
A careful evaluation by our epileptologist and neurosurgeons, using the most advanced imaging and diagnosing available, we will assess your child’s surgery prospects. After mapping your child’s brain and unique epilepsy pinpointing the source of seizures, our team will discuss the options that offer your child the best possible outcomes.
No, our goal is to keep your child safe. A seizing brain isn’t a developing brain, and we strive to optimize your child’s developmental potential. Surgery should never be a last resort, rather a necessary part of the treatment plan.
