Chapters 18-25 Flashcards
How are gliomas classified?
Location of Glioma
Grade: 1 & 2 are low grade, slow growing, tend to be benign (better prognosis)
3 & 4 are high grade, fast growing, spreads to norm. brain tissue, tends to be malignant
What are two types of Tumors?
Giloma
Neuroblastoma
What is the survival rate for someone with a high grade glioma?
1-3 years
What is the survival rate of grade 1 and 2 (low grade) gliomas?
11-16 years
What are some signs and symptoms of glioma?
Located in Brain: Headache, Seizure, Nausea, Vomiting
Located in Spine: Pain, Weakness, Numbness, Tingling
What is the definition of a Glioma?
Tumor of the glial tissue of the nervous system.
Define Neuroblastoma.
Tumor composed of neuroblasts (Most commonly found in the adrenal gland).
What are some signs and symptoms of Neuroblastoma?
Some of the 1st signs are: Fever, Malaise, Pain, Loss of Appetite, Weight Loss and Diarrhea.
As the disease progresses (Depending on where the tumor is located): Bone Pain, Diff. Breathing/ Chronic Cough, Enlarged Abdomen, Flushed/ Red Skin, Pale Skin with Blue Coloring Around the Eyes, Profuse Sweating and Tachycardia.
When is a neuroblastoma found?
It is found through an ultrasound while the baby is still in the womb. If it is not found before birth then the child is anywhere from 1-3 yrs. old before it is found.
What is Amyotrophic Lateral Sclerosis (ALS)?
A progressive degeneration of the motor neurons of the central nervous system, leading to wasting of the muscles and paralysis.
What age does ALS usually occur and who is apt to get it?
Usual age of onset is 35 yrs old. Men are 2-3x more likely to get it than women.
What are some signs and symptoms of ALS?
Muscle weakness in one or more of the following: hands, arms, legs or the muscles of speech, swallowing or breathing
Twitching (fasciculation) and cramping of muscles, especially those in the hands and feet
Impairment of the use of the arms and legs
“Thick speech” and difficulty in projecting the voice
In more advanced stages, shortness of breath, difficulty in breathing and swallowing
How is ALS diagnosed?
A neurologist will administer an electromyogram (EMG), which is used to detect nerve damage. Additional tests can rule out muscular dystrophy, multiple sclerosis, spinal cord tumors, or other diseases.
*Also the doctor may order a biopsy of a wasted away muscle.
What is Amyotrophic Lateral Sclerosis (ALS) also referred to as?
Lou Gehrig’s Disease
What therapy is involved in caring for someone with ALS?
Therapy provided Equipment Needs
Provides Caregiver and Patient Education about the disease and how to care for themselves/ patient.
Define Alzheimer’s Disease.
A progressive mental deterioration that can occur in middle or old age, due to generalized degeneration of the brain. It is the most common form of Dementia.
What are some signs and symptoms of Alzheimer’s?
Short Term Memory Loss, Confusion, Irritability
As the disease progresses: Aggressive, Mood Swings, Forget Words, Long Term Memory Loss
What is the common age range of onset of Alzheimer’s and who is more apt to get it?
Onset usually occurs after the age of 65 yrs. old. Affects men just as much as women.
What is the life expectancy of a patient with Alzheimer’s?
7-14 years
What is the definition of Huntington’s Disease?
A hereditary disease marked by degeneration of the brain cells and causing chorea (jerky involuntary movements affecting especially the shoulders, hips, and face) and progressive dementia.
In what age range does Huntington’s usually appear?
35-44 years of age
Who is more apt to have Huntington’s Disease?
Men are more apt to have this than women. Those of European decent are also more apt to have this.
What is the average life expectancy of someone who is diagnosed with Huntington’s Disease?
20 years
What are some signs and symptoms of Huntington’s Disease?
Slight uncontrollable movements. Clumsiness. Stumbling. Some slight signs of lack of emotion. Lack of focus, slight concentration problems. Lapses in short-term memory. Depression. Mood changes - this may include antisocial behavior and aggression.
How is Huntington’s Treated?
(NO CURE)
Medication is used to relieve symptoms.
Define Parkinson’s Disease.
A disorder of the brain that leads to shaking (tremors) and difficulty with walking, movement, and coordination.
What age range does the onset of Parkinson’s occur?
55-60 years old
What are the Cardinal Signs of Parkinson’s Disease?
Tremors (Most Common), Rigidity (resistance to limb movements), and Movement Slowness (the person has difficulty planning and initiating their movements)
What kind of Medical Management is offered for one with Parkinson’s?
Medicines that mimic dopamine that the body is missing.
Deep Brain Stimulator (Last resort when meds no longer work)
Physical Therapy that addresses ROM, Gait, Balance etc as well as education for the patient and pt. family.
Define Multiple Sclerosis (MS).
A chronic, typically progressive disease involving damage to the sheaths of nerve cells in the brain and spinal cord.
What are some common signs and symptoms of MS?
Symptoms may include numbness, impairment of speech and of muscular coordination, blurred vision, and severe fatigue.
What is the common age range of onset for MS?
30-60 yrs old but has been know to show up in people as young as 10.