Seizures: Pathology review

22,059views

Seizures: Pathology review

Watch later

Watch later

Nervous system anatomy and physiology
Sympathetic nervous system
Parasympathetic nervous system
Central nervous system histology
Peripheral nervous system histology
Cardiac muscle histology
Respiratory system anatomy and physiology
Introduction to the immune system
Innate immune system
Seizures and epilepsy
Migraine
Alzheimer disease
Vascular dementia
Frontotemporal dementia
Dementia with Lewy bodies
Kluver-Bucy syndrome
Multiple sclerosis
Neurogenic bladder
Brown-Sequard Syndrome
Parkinson disease
Acoustic neuroma (schwannoma)
Spinal muscular atrophy
Myasthenia gravis
Sciatica
Carpal tunnel syndrome
Horner syndrome
Pediatric brain tumors
Eustachian tube dysfunction
Cardiovascular system anatomy and physiology
Glaucoma
Anatomy and physiology of the ear
Anatomy and physiology of the eye
Adrenergic receptors
Cholinergic receptors
Pyramidal and extrapyramidal tracts
Basal ganglia: Direct and indirect pathway of movement
Muscle spindles and golgi tendon organs
Cerebellum
Somatosensory receptors
Optic pathways and visual fields
Vestibular transduction
Olfactory transduction and pathways
Somatosensory pathways
Photoreception
Auditory transduction and pathways
Vestibulo-ocular reflex and nystagmus
Taste and the tongue
Cranial nerves
Body temperature regulation (thermoregulation)
Breathing cycle and regulation
Action potentials in myocytes
Action potentials in pacemaker cells
Cardiac excitation-contraction coupling
Excitability and refractory periods
Cardiac conduction system
Cardiac conduction velocity
ECG basics
ECG intervals
ECG axis
ECG rate and rhythm
ECG QRS transition
ECG normal sinus rhythm
ECG cardiac hypertrophy and enlargement
ECG cardiac infarction and ischemia
Adrenocorticotropic hormone
Oxytocin and prolactin
Growth hormone and somatostatin
Antidiuretic hormone
Insulin
Glucagon
Testosterone
Estrogen and progesterone
Gastrointestinal system anatomy and physiology
Anatomy and physiology of the teeth
Liver anatomy and physiology
Enteric nervous system
Gastric motility
Esophageal motility
Chewing and swallowing
Fats and lipids
Carbohydrates and sugars
Proteins
Pancreatic secretion
Prebiotics and probiotics
Bile secretion and enterohepatic circulation
Blood components
Blood groups and transfusions
Platelet plug formation (primary hemostasis)
Role of Vitamin K in coagulation
Coagulation (secondary hemostasis)
Clot retraction and fibrinolysis
Cytokines
Complement system
T-cell development
MHC class I and MHC class II molecules
T-cell activation
B-cell development
B-cell activation, differentiation, and contraction
Cell-mediated immunity of CD4 cells
Cell-mediated immunity of natural killer and CD8 cells
Somatic hypermutation and affinity maturation
Antibody classes
VDJ rearrangement
Contracting the immune response and peripheral tolerance
B- and T-cell memory
Skin anatomy and physiology
Wound healing
Hair, skin and nails
Skeletal system anatomy and physiology
Cartilage structure and growth
Bone remodeling and repair
Fibrous, cartilage, and synovial joints
Muscular system anatomy and physiology
Neuromuscular junction and motor unit
Slow twitch and fast twitch muscle fibers
Muscle contraction
Sliding filament model of muscle contraction
Brachial plexus
Neuron action potential
Cerebral circulation
Ascending and descending spinal tracts
Renal system anatomy and physiology
Hydration
Movement of water between body compartments
Body fluid compartments
Renal clearance
Regulation of renal blood flow
Glomerular filtration
Measuring renal plasma flow and renal blood flow
Tubular reabsorption of glucose
Tubular secretion of PAH
Urea recycling
Proximal convoluted tubule
Distal convoluted tubule
Loop of Henle
Renin-angiotensin-aldosterone system
Sodium homeostasis
Phosphate, calcium and magnesium homeostasis
Potassium homeostasis
Osmoregulation
Kidney countercurrent multiplication
Erythropoietin
Physiologic pH and buffers
The role of the kidney in acid-base balance
Buffering and Henderson-Hasselbalch equation
Acid-base map and compensatory mechanisms
Respiratory acidosis
Plasma anion gap
Metabolic acidosis
Respiratory alkalosis
Metabolic alkalosis
Anatomy and physiology of the male reproductive system
Puberty and Tanner staging
Anatomy and physiology of the female reproductive system
Menopause
Pregnancy
Stages of labor
Breastfeeding
Lung volumes and capacities
Anatomic and physiologic dead space
Alveolar surface tension and surfactant
Ventilation
Regulation of pulmonary blood flow
Ventilation-perfusion ratios and V/Q mismatch
Pulmonary shunts
Zones of pulmonary blood flow
Diffusion-limited and perfusion-limited gas exchange
Airflow, pressure, and resistance
Gas exchange in the lungs, blood and tissues
Alveolar gas equation
Oxygen binding capacity and oxygen content
Oxygen-hemoglobin dissociation curve
Carbon dioxide transport in blood
Muscle weakness: Clinical
Bone histology
Skeletal muscle histology
Cartilage histology
Gout and pseudogout: Pathology review
Glucocorticoids
Non-steroidal anti-inflammatory drugs
Opioid agonists, mixed agonist-antagonists and partial agonists
Antigout medications
Prostate gland histology
Penis histology
Testis, ductus deferens, and seminal vesicle histology
Mammary gland histology
Fallopian tube and uterus histology
Cervix and vagina histology
Ovary histology
Menstrual cycle
Prostate cancer
Benign prostatic hyperplasia
Erectile dysfunction
Amenorrhea
Androgens and antiandrogens
Adrenergic antagonists: Alpha blockers
PDE5 inhibitors
Estrogens and antiestrogens
Progestins and antiprogestins
Aromatase inhibitors
Uterine stimulants and relaxants
Thyroid and parathyroid gland histology
Adrenal gland histology
Pituitary gland histology
Pancreas histology
Hyperthyroidism medications
Hypothyroidism medications
Insulins
Miscellaneous hypoglycemics
Hypoglycemics: Insulin secretagogues
Adrenal hormone synthesis inhibitors
Mineralocorticoids and mineralocorticoid antagonists
Blood histology
Spleen histology
Lymph node histology
Thymus histology
Skin histology
Ureter, bladder and urethra histology
Kidney histology
Nasal cavity and larynx histology
Bronchioles and alveoli histology
Trachea and bronchi histology
Introduction to biostatistics
Probability
Types of data
Mean, median, and mode
Standard error of the mean (Central limit theorem)
Range, variance, and standard deviation
Normal distribution and z-scores
Paired t-test
Hypothesis testing: One-tailed and two-tailed tests
Two-way ANOVA
Correlation
Linear regression
Two-sample t-test
One-way ANOVA
Repeated measures ANOVA
Methods of regression analysis
Logistic regression
Type I and type II errors
Sensitivity and specificity
Test precision and accuracy
Positive and negative predictive value
Incidence and prevalence
Odds ratio
Mortality rates and case-fatality
Direct standardization
Relative and absolute risk
DALY and QALY
Indirect standardization
Study designs
Ecologic study
Case-control study
Clinical trials
Cross sectional study
Cohort study
Sample size
Disease causality
Information bias
Interaction
Selection bias
Confounding
Prevention
Control of blood flow circulation
Cardiac and vascular function curves
Altering cardiac and vascular function curves
Baroreceptors
Laminar flow and Reynolds number
Resistance to blood flow
Pressures in the cardiovascular system
Blood pressure, blood flow, and resistance
Compliance of blood vessels
Microcirculation and Starling forces
Measuring cardiac output (Fick principle)
Cardiac contractility
Cardiac preload
Law of Laplace
Stroke volume, ejection fraction, and cardiac output
Frank-Starling relationship
Cardiac afterload
Cardiac cycle
Pressure-volume loops
Physiological changes during exercise
Cardiac work
Changes in pressure-volume loops
Chemoreceptors
Endocrine system anatomy and physiology
Synthesis of adrenocortical hormones
Cortisol
Vitamin D
Adrenal insufficiency: Pathology review
Adrenal masses: Pathology review
Hyperthyroidism: Pathology review
Hypothyroidism: Pathology review
Thyroid nodules and thyroid cancer: Pathology review
Parathyroid disorders and calcium imbalance: Pathology review
Diabetes mellitus: Pathology review
Cushing syndrome and Cushing disease: Pathology review
Pituitary tumors: Pathology review
Hypopituitarism: Pathology review
Diabetes insipidus and SIADH: Pathology review
Multiple endocrine neoplasia: Pathology review
Congenital gastrointestinal disorders: Pathology review
Esophageal disorders: Pathology review
GERD, peptic ulcers, gastritis, and stomach cancer: Pathology review
Inflammatory bowel disease: Pathology review
Malabsorption syndromes: Pathology review
Diverticular disease: Pathology review
Appendicitis: Pathology review
Gastrointestinal bleeding: Pathology review
Colorectal polyps and cancer: Pathology review
Pancreatitis: Pathology review
Jaundice: Pathology review
Viral hepatitis: Pathology review
Cirrhosis: Pathology review
Microcytic anemia: Pathology review
Non-hemolytic normocytic anemia: Pathology review
Intrinsic hemolytic normocytic anemia: Pathology review
Extrinsic hemolytic normocytic anemia: Pathology review
Macrocytic anemia: Pathology review
Coagulation disorders: Pathology review
Platelet disorders: Pathology review
Mixed platelet and coagulation disorders: Pathology review
Thrombosis syndromes (hypercoagulability): Pathology review
Lymphomas: Pathology review
Leukemias: Pathology review
Plasma cell disorders: Pathology review
Myeloproliferative disorders: Pathology review
Immunodeficiencies: Combined T-cell and B-cell disorders: Pathology review
Immunodeficiencies: Phagocyte and complement dysfunction: Pathology review
Pigmentation skin disorders: Pathology review
Acneiform skin disorders: Pathology review
Papulosquamous and inflammatory skin disorders: Pathology review
Vesiculobullous and desquamating skin disorders: Pathology review
Skin cancer: Pathology review
Back pain: Pathology review
Rheumatoid arthritis and osteoarthritis: Pathology review
Seronegative and septic arthritis: Pathology review
Systemic lupus erythematosus (SLE): Pathology review
Scleroderma: Pathology review
Sjogren syndrome: Pathology review
Bone disorders: Pathology review
Bone tumors: Pathology review
Myalgias and myositis: Pathology review
Neuromuscular junction disorders: Pathology review
Muscular dystrophies and mitochondrial myopathies: Pathology review
Vitamin B12 deficiency
Friedreich ataxia
Syringomyelia
Charcot-Marie-Tooth disease
Guillain-Barre syndrome
Lambert-Eaton myasthenic syndrome
Congenital neurological disorders: Pathology review
Headaches: Pathology review
Seizures: Pathology review
Cerebral vascular disease: Pathology review
Traumatic brain injury: Pathology review
Spinal cord disorders: Pathology review
Dementia: Pathology review
Central nervous system infections: Pathology review
Movement disorders: Pathology review
Demyelinating disorders: Pathology review
Adult brain tumors: Pathology review
Pediatric brain tumors: Pathology review
Neurocutaneous disorders: Pathology review

Transcript

Watch video only

On the neurology ward, a 7-year old male, called Stefan, is brought by his mother. His mother is worried because he has several episodes every day where he loses consciousness for a few seconds. His teacher also complains that she often catches him daydreaming during the lesson. Next to Stefan, there’s a 17-year old male, called Jacob, who seems sluggish and tired. His friends brought him because he suddenly started “shaking and jerking” and he lost consciousness for about two minutes. His medical history is otherwise insignificant. Now, there’s also an 11-year old female, called Megan, who also seems lethargic. Her father is very upset because he witnessed an episode of twitching of her left foot that lasted a few minutes. Megan was unconscious and has no memory of the event. Finally, there’s a 19-year old female, called Joanna, that has had repetitive episodes of sudden and rapid jerking movements with loss of consciousness for the past few months. They usually occur when she wakes up in the morning and especially during periods of sleep deprivation.

Okay, so all of them had a seizure episode. A seizure is a paroxysmal motor, sensory or autonomic event that occurs due to abnormal, excessive and synchronous electrical discharges from neurons in the brain. Seizures usually last less than 5 minutes. If it lasts more than 5 minutes, it’s called status epilepticus. Epilepsy is a chronic disease of the brain that predisposes an individual to having recurrent unprovoked seizures; that is seizures without a clear triggering cause. Epilepsy is typically diagnosed when an individual has two or more unprovoked seizures separated by at least twenty-four hours.

Okay, now seizures are broadly classified into two types, generalized and focal seizures. Generalized seizures arise from both cerebral hemispheres at the same time, while focal seizures arise from specific areas in one cerebral hemisphere. However, focal seizures can spread to both cerebral hemispheres, causing a generalized seizure. When this happens, it’s appropriately called secondary generalization of a focal seizure.

Okay, now let’s take a closer look at the different subtypes of generalized seizures. Generalized seizures are subclassified into motor and non-motor seizures. Regardless of the subtype, generalized seizures almost always cause a sudden impairment of consciousness. Generalized motor seizures include tonic, clonic, tonic-clonic, atonic, and myoclonic seizures. Tonic seizures involve sudden stiffening of the muscles, while clonic seizures involve rhythmic twitching of the muscles. However, these clinical features are usually combined, so individuals commonly have a tonic-clonic seizure. In a generalized tonic-clonic seizure, a person may have a sudden contraction of their vocal cord muscles, causing them to involuntarily scream or cry during a seizure. Contraction of the ocular muscles can cause uprolling of the eyes. Contraction of the oropharyngeal muscles can impair swallowing, causing respiratory secretions to pool in the oropharynx. Contraction of the jaw muscles may cause the individual to bite on their tongue. Individuals with tonic-clonic seizures may also develop urinary or fecal incontinence. After the tonic-clonic seizure ends, individuals enter a period called the post-ictal phase, during which the individual’s consciousness is still impaired for minutes to hours, so they seem sluggish and tired or hard to wake up. So on the exam, look for these subtle clues that indicate a post-ictal phase. Next are myoclonic seizures. For the test, remember that myoclonic seizures involve sudden, rapid, muscle contractions. This sounds a lot like clonic seizures, but the key difference is that in myoclonic seizures, the contractions are much faster, occurring at a rate of 0.1 seconds, whereas in clonic seizures, the contractions occur at a rate of about 1 to 2 seconds. Myoclonic seizures typically occur in the morning and are usually triggered by stress or sleep deprivation, and that’s something you also have to know for the exams! Alright, now atonic seizures translates to “no muscle tone”. Therefore they are characterized by sudden loss of postural muscle tone lasting 1 to 2 seconds, causing the individual to collapse to the ground out of the blue. Alright, moving on to the other arm of generalized seizures, there are the generalized non-motor seizures. These are called absence seizures and they are very high yield. They are commonly found in children and adolescents. Episodes are characterized by sudden, brief loss of consciousness for seconds to minutes without any change in the individual’s muscle tone. So, they could be sitting in class listening to a lecture and suddenly lose consciousness without falling down. Unfortunately, episodes can occur dozens or even hundreds of times per day, and are classically described by parents and teachers as “staring into space”, or “daydreaming”, or being “inattentive”. In fact, many children with absence seizures are actually misdiagnosed with attention-deficit hyperactivity disorder, because teachers often presume that a child is just not paying attention.

Okay, now another high yield topic is focal seizures, previously called partial seizures. Focal seizures are classified into those that do not impair consciousness,, and those that impair consciousness. Focal seizures that impair consciousness are also followed by a post-ictal phase, whereas focal seizures that didn’t affect consciousness do not have a postictal phase. Now, focal seizures can be motor, sensory, or autonomic, depending on the area of the cerebral cortex involved. For example, a focal seizure involving the primary motor cortex may cause tonic or clonic movements of the contralateral extremity, whereas a focal seizure involving the occipital cortex may cause someone to see flashing lights. Sometimes, focal seizures may begin as subtle neurological symptoms called auras. During an aura, individuals may exhibit subtle muscle movements called automatisms, such as chewing, lip smacking, or rapid blinking of the eyes. Other interesting forms of aura include smelling unusual odors like kerosene, a rising sensation in abdomen, or even feelings of fear or deja vu. Also, an interesting phenomenon that occurs after focal motor seizures is Todd’s paralysis, which describes a temporary paralysis of the affected extremity. Alright, now it might be difficult to know if a seizure was a generalized tonic-clonic right from the beginning, or if it was a focal seizure that secondarily generalized. However, a history of an aura, unilateral shaking, turning of the head to one side or Todd’s paralysis is a clue it may have been a focal seizure that secondarily generalized. Take that with a grain of salt though, because the absence of these historical features does not adequately exclude a focal seizure.

Okay, now a special subtype of seizures that occurs in young children between the ages of 6 months and 5 years are febrile seizures. These only happen when the child develops a fever, and they can be generalized or focal. Because of this, febrile seizures are classified differently, and include simple and complex febrile seizures. Simple febrile seizures are usually generalized, last less than 15 minutes, and do not happen again within 24 hours. Complex febrile seizures are usually focal in onset, last more than 15 minutes, and often happen more than once in the span of 24 hours. For your exam, remember that infection with human herpes virus 6 or HHV-6 has a particularly high association with febrile seizures. This virus also causes roseola infantum, a disease characterized by the development a high grade fever for about 3 to 5 days, then the fever goes away and a maculopapular rash appears on the trunk and spreads to the extremities. So remember, fever first, rash later. Diagnostic investigations focus on looking for the cause of fever and excluding serious pathology. For example, a lumbar puncture may be performed to exclude meningitis.

Key Takeaways

A seizure is a paroxysmal event due to abnormal electrical activity in the brain that can cause changes in behavior, consciousness, or movement. A seizure shouldn't be confused with epilepsy, which is said when two or more unprovoked seizures occur. Epilepsy is a chronic disorder that predisposes the individual to have recurrent seizures, and can't be diagnosed based on a single episode of seizures alone.

Seizures can be classified into generalized and focal seizures. Generalized seizures arise from both cerebral hemispheres at the same time, and almost always cause a sudden impairment of consciousness; whereas focal seizures arise from specific areas in one cerebral hemisphere, and present as a dysfunction of the part of the body controlled by the affected part of the brain.

When evaluating an individual with seizures, it's first important to identify the possible trigger. Diagnostic tests such as a CBC (complete blood count), electrolytes, liver function tests, and glucose levels, must be done to reveal potential causes. An EEG (electroencephalography) can also be done to assess the type of seizure. Treatment for seizures may involve supportive therapy, treating the underlying causes when possible, and antiseizure medications to manage convulsions.

Sources

  1. "Robbins Basic Pathology" Elsevier (2017)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
  4. "DeGowin's Diagnostic Examination, Tenth Edition" McGraw-Hill Education / Medical (2014)
  5. "Epilepsy" Lippincott Williams & Wilkins (2007)
  6. "Cochrane Database of Systematic Reviews"
  7. "Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy" Neuroscience Bulletin (2017)
  8. "The Blood?Brain Barrier and Epilepsy" Epilepsia (2006)