Seizures: Pathology review

Last updated: September 12, 2024

Seizures: Pathology review

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Anatomical terminology
Joints of the ankle and foot
Anatomy of the tibiofibular joints
DNA structure
DNA replication
Hair, skin and nails
Wound healing
Estrogens and antiestrogens
Skin cancer
Chronic granulomatous disease
Plasmodium species (Malaria)
VDJ rearrangement
Bile secretion and enterohepatic circulation
Normal heart sounds
Ascending and descending spinal tracts
Somatosensory pathways
Anatomy of the diencephalon
Independent assortment of genes and linkage
Anatomy of the cerebral cortex
Anatomy of the ventricular system
Basal ganglia: Direct and indirect pathway of movement
Anatomy of the basal ganglia
Anatomy of the descending spinal cord pathways
Anatomy of the ascending spinal cord pathways
Movement disorders: Pathology review
Eye conditions: Refractive errors, lens disorders and glaucoma: Pathology review
Anatomy of the eye
Anatomy of the oculomotor (CN III), trochlear (CN IV) and abducens (CN VI) nerves
Anatomy and physiology of the ear
Auditory transduction and pathways
Anatomy of the inner ear
Ischemic stroke
Stroke: Clinical
Anatomy of the brainstem
Anatomy of the limbic system
Pediatric ophthalmological conditions: Clinical
Anatomy of the nose and paranasal sinuses
Schizophrenia spectrum disorders: Clinical
Spinocerebellar ataxia (NORD)
Anatomy clinical correlates: Cerebellum and brainstem
Anatomy of the pharynx and esophagus
Somatic symptom disorders: Clinical
Malingering, factitious disorders and somatoform disorders: Pathology review
Factitious disorder
Major depressive disorder
Suicide
Major depressive disorder with seasonal pattern
Insomnia
Developmental and learning disorders: Pathology review
Childhood and early-onset psychological disorders: Pathology review
Disorders of consciousness: Clinical
Brain herniation
Epidural hematoma
Subdural hematoma
Subarachnoid hemorrhage
Hernias: Clinical
Hypothyroidism
ADHD: Information for patients and families (The Primary School)
Attention deficit hyperactivity disorder
Neurodevelopmental disorders: Clinical
Autism spectrum disorder
Bipolar and related disorders
Mood disorders: Clinical
Pediatric upper airway conditions: Clinical
Upper respiratory tract infection
Superficial structures of the neck: Anterior triangle
Superficial structures of the neck: Posterior triangle
Anxiety disorders: Clinical
Anxiety disorders, phobias and stress-related disorders: Pathology Review
Generalized anxiety disorder
Anatomy of the facial nerve (CN VII)
Bell palsy
Cranial nerves rap
Anatomy of the infratemporal fossa
Anatomy of the trigeminal nerve (CN V)
Temporomandibular joint dysfunction
Anatomy of the temporomandibular joint and muscles of mastication
Allergic rhinitis
Nasal polyps
Sinusitis
Rhinovirus
Nasal, oral and pharyngeal diseases: Pathology review
Pancoast tumor
Laryngitis
Laryngomalacia
Trauma- and stress-related disorders: Pathology review
Trauma- and stressor-related disorders: Clinical
Traumatic brain injury: Clinical
Dementia: Pathology review
Meningitis
Meningitis, encephalitis and brain abscesses: Clinical
Abscesses
Seizures: Pathology review
Seizures: Clinical
Febrile seizure
Sleep disorders: Clinical
Narcolepsy (NORD)
Sleep apnea
Syncope: Clinical
Anatomy clinical correlates: Oculomotor (CN III), trochlear (CN IV) and abducens (CN VI) nerves
Kidney histology
Hypertension
Movement of water between body compartments
Body fluid compartments
Glucocorticoids
Mineralocorticoids and mineralocorticoid antagonists
Adrenocorticotropic hormone
Regulation of renal blood flow
Hydration
Synthesis of adrenocortical hormones
Cortisol
Vitamin D
Renal system anatomy and physiology
Renal clearance
Complement system
Hyponatremia
Hyponatremia: Clinical
Hypernatremia
Hypernatremia: Clinical
Electrolyte disturbances: Pathology review
Hypokalemia
Hypokalemia: Clinical
Hyperkalemia
Hyperkalemia: Clinical
Action potentials in myocytes
Cardiac conduction system
Hyperparathyroidism
ECG cardiac infarction and ischemia
Myocardial infarction
Pericarditis and pericardial effusion
Pleural effusion
Long QT syndrome and Torsade de pointes
Cardiovascular: Pulse (for nursing assistant training)
Atherosclerosis and arteriosclerosis: Pathology review
Arterial disease
Aneurysms
Ischemia
Deep vein thrombosis
Familial hypercholesterolemia
Hypercholesterolemia: Clinical
Dyslipidemias: Pathology review
Kidney countercurrent multiplication
Insulins
Diabetes mellitus
Diabetes mellitus: Pathology review
Pulmonary embolism
Deep vein thrombosis and pulmonary embolism: Pathology review
Wolff-Parkinson-White syndrome
Thyroid and parathyroid gland histology
Thyroid hormones
Hypothyroidism: Pathology review
Hyperthyroidism: Pathology review
Hyperthyroidism: Clinical
Toxic multinodular goiter
Thyroid nodules and thyroid cancer: Clinical
Coagulation (secondary hemostasis)
Platelet plug formation (primary hemostasis)
Helping a patient with a rare disease
Diabetes mellitus: Clinical
Pancreas histology
Pancreatic secretion
Endocrine system anatomy and physiology
Miscellaneous hypoglycemics
Hypopituitarism
Hypopituitarism: Pathology review
Hypopituitarism: Clinical
Pituitary adenoma
Acromegaly
Gigantism
Diabetes insipidus and SIADH: Pathology review
Hypoglycemics: Insulin secretagogues
Liver histology
Liver anatomy and physiology
Cirrhosis
Cirrhosis: Pathology review
Cirrhosis: Clinical
Alcohol-associated liver disease
Primary biliary cholangitis
Parathyroid disorders and calcium imbalance: Pathology review
Phosphate, calcium and magnesium homeostasis
Parathyroid conditions and calcium imbalance: Clinical
Parathyroid hormone
Hypocalcemia
Hypercalcemia
Jaundice
Jaundice: Pathology review
Jaundice: Clinical
Hepatitis A and Hepatitis E virus
Hepatitis B and Hepatitis D virus
Hepatitis C virus
Adrenal gland histology
Primary adrenal insufficiency
Adrenal insufficiency: Pathology review
Adrenal insufficiency: Clinical
Cushing syndrome and Cushing disease: Pathology review
Cushing syndrome
Pheochromocytoma
Hyperaldosteronism
Gallstone ileus
Gallstones
Gallbladder disorders: Pathology review
Biliary colic
Ascending cholangitis
Gastrointestinal system anatomy and physiology
Clinical Skills: Abdominal Assessment
GERD, peptic ulcers, gastritis, and stomach cancer: Pathology review
Peptic ulcers and stomach cancer: Clinical
Gastric cancer
Gastrointestinal bleeding: Pathology review
Gastrointestinal bleeding: Clinical
Hashimoto thyroiditis
Chronic pancreatitis
Pancreatitis: Pathology review
Pancreatitis: Clinical
Acute pancreatitis
Pancreatic cancer
Malabsorption syndromes: Pathology review
Malabsorption: Clinical
Celiac disease
Short bowel syndrome (NORD)
Esophageal disorders: Clinical
Esophageal disorders: Pathology review
Gastroesophageal reflux disease (GERD)
Gastroesophageal reflux disease (GERD): Clinical
Eosinophilic esophagitis (NORD)
Diverticular disease: Pathology review
Anatomy of the gastrointestinal organs of the pelvis and perineum
Lesch-Nyhan syndrome
Sjogren syndrome
Non-steroidal anti-inflammatory drugs
Antihistamines for allergies
Eczematous rashes: Clinical
Atopic dermatitis
Urinary tract infections: Pathology review
Urinary tract infections: Clinical
Lower urinary tract infection
Papulosquamous and inflammatory skin disorders: Pathology review
Mechanisms of antibiotic resistance
Erythema multiforme
Congenital TORCH infections: Pathology review
Severe chronic neutropenia (NORD)
Lung cancer
Immunodeficiencies: Combined T-cell and B-cell disorders: Pathology review
Immunodeficiencies: Clinical
Anaphylaxis
Epigenetics
Cell signaling pathways
Cell cycle
Necrosis and apoptosis
Human papillomavirus
Atrophy, aplasia, and hypoplasia
Estrogen and progesterone
Testosterone
Androgens and antiandrogens
Anatomy of the female urogenital triangle
Anatomy of the female reproductive organs of the pelvis
Anatomy and physiology of the female reproductive system
Cellulitis and erysipelas: Clinical sciences
Mesoderm
Development of the axial skeleton
Spinal cord disorders: Pathology review
Chest trauma: Clinical
Shock: Pathology review
Shock
Hypovolemic shock: Clinical sciences
Portal hypertension
Metabolic acidosis
Pulmonary embolism: Clinical sciences
Marfan syndrome
Anticoagulants: Heparin
Anticoagulants: Warfarin
Abdominal aortic aneurysm: Clinical sciences
Reading a chest X-ray
Chest X-ray interpretation: Clinical sciences
Approach to dyspnea: Clinical sciences
Bulimia nervosa
Anorexia nervosa
Lung volumes and capacities
Deep vein thrombosis: Clinical sciences
ECG basics
Multiple organ dysfunction syndrome (MODS): Clinical sciences
Sepsis: Clinical sciences
Stomach histology
Approach to non-healing wounds: Clinical sciences
Assessment of Thorax and Lungs
Bacterial and viral skin infections: Pathology review
Cellulitis
Necrotizing soft tissue infections: Clinical sciences
Necrotizing fasciitis
Clostridium perfringens
General anesthetics
Local anesthetics
Nitrogen and urea cycle
Surgical site infection: Clinical sciences
Disseminated intravascular coagulation
Congenital neurological disorders: Pathology review
Puberty and Tanner staging
Precocious puberty
Turner syndrome
Turner syndrome: Year of the Zebra
Disorders of sexual development and sex hormones: Pathology review
Congenital adrenal hyperplasia
5-alpha-reductase deficiency
Klinefelter syndrome
Disorders of sex chromosomes: Pathology review
Brachial plexus
Neonatal meningitis
Development of the fetal membranes
cGMP mediated smooth muscle vasodilators
Down syndrome (Trisomy 21)
Autosomal trisomies: Pathology review
Taking a good patient history
Chlamydia trachomatis infection: Clinical sciences
Sexually transmitted infections: Vaginitis and cervicitis: Pathology review
Neisseria gonorrhoeae infection: Clinical sciences
Testis, ductus deferens, and seminal vesicle histology
Anatomy and physiology of the male reproductive system
Hypoparathyroidism
Protein-calorie malnutrition: Clinical sciences
Zinc deficiency and protein-energy malnutrition: Pathology review
Water-soluble vitamin deficiency and toxicity: B1-B7: Pathology review
Water-soluble vitamin deficiency and toxicity: B9, B12 and vitamin C: Pathology review
Fat-soluble vitamin deficiency and toxicity: Pathology review
Disorders of carbohydrate metabolism: Pathology review
Galactosemia
Cholestatic liver disease
Infectious gastroenteritis: Clinical sciences
Cyclic vomiting syndrome (NORD)
Viral hepatitis
Hepatitis medications
Hepatitis C: Clinical sciences
Uremic encephalopathy: Clinical sciences
Alagille syndrome (NORD)
Alagille syndrome (NORD): Year of the Zebra
Adrenal insufficiency: Clinical sciences
Achondroplasia
Anatomy of the lymphatics of the neck
Anatomy of the inguinal region
Lymphatic system anatomy and physiology
Introduction to the lymphatic system
Kawasaki disease
Bordetella pertussis (Whooping cough)
Cystic fibrosis: Pathology review
Miscellaneous genetic disorders: Pathology review
Fragile X syndrome
Measles virus
Epstein-Barr virus (Infectious mononucleosis)
Disruptive, impulse control, and conduct disorders
Approach to syncope: Clinical sciences
Glycogen storage disease type I
Glycogen storage disease type II (NORD)
Disorders of fatty acid metabolism: Pathology review
Spinal muscular atrophy
Approach to urinary incontinence (GYN): Clinical sciences
Approach to hypothyroidism: Clinical sciences
Hypothyroidism medications
Approach to hyperthyroidism and thyrotoxicosis: Clinical sciences
Thyroid carcinoma: Clinical sciences
Anatomy clinical correlates: Anterior and posterior abdominal wall
Approach to abdominal wall and groin masses: Clinical sciences
Inguinal hernias: Clinical sciences
Approach to a postoperative fever: Clinical sciences
Chronic venous insufficiency
Venous insufficiency and ulcers: Clinical sciences

Transcript

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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)