Seizures: Pathology review

22,056views

Seizures: Pathology review

Ting å sjå

Ting å sjå

Physical and sexual abuse
Schizoaffective disorder
Schizophreniform disorder
Delirium
Cluster A personality disorders
Cluster C personality disorders
Cluster B personality disorders
Somatic symptom disorder
Insomnia
Vitamin D deficiency
Folate (Vitamin B9) deficiency
Vitamin B12 deficiency
Wernicke-Korsakoff syndrome
Normal heart sounds
Abnormal heart sounds
ECG cardiac infarction and ischemia
ECG cardiac hypertrophy and enlargement
Brugada syndrome
Endocarditis
Hypothyroidism
Hyperparathyroidism
Diabetes mellitus
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Hyperthyroidism: Pathology review
Introduction to the cranial nerves
Glaucoma
Otitis media
Otitis externa
Vertigo
Labyrinthitis
Acoustic neuroma (schwannoma)
Gastroesophageal reflux disease (GERD)
Vertigo: Pathology review
Nasal, oral and pharyngeal diseases: Pathology review
Parathyroid disorders and calcium imbalance: Pathology review
Eye conditions: Inflammation, infections and trauma: Pathology review
Acid reducing medications
Anatomy of the abdominal viscera: Liver, biliary ducts and gallbladder
Anatomy of the inguinal region
Barrett esophagus
Zenker diverticulum
Peptic ulcer
Gastric cancer
Crohn disease
Ulcerative colitis
Bowel obstruction
Abdominal hernias
Irritable bowel syndrome
Diverticulosis and diverticulitis
Appendicitis
Gastroenteritis
Hemorrhoid
Gallstones
Acute cholecystitis
Chronic cholecystitis
Acute pancreatitis
Congenital gastrointestinal disorders: Pathology review
Esophageal disorders: Pathology review
Inflammatory bowel disease: Pathology review
Diverticular disease: Pathology review
Gastrointestinal bleeding: Pathology review
Pancreatitis: Pathology review
Jaundice: Pathology review
Gallbladder disorders: Pathology review
Appendicitis: Pathology review
GERD, peptic ulcers, gastritis, and stomach cancer: Pathology review
Laxatives and cathartics
Antidiarrheals
Platelet plug formation (primary hemostasis)
Coagulation (secondary hemostasis)
Role of Vitamin K in coagulation
Clot retraction and fibrinolysis
Coagulation disorders: Pathology review
Iron deficiency anemia
Anemia of chronic disease
Hemophilia
Hemolytic-uremic syndrome
Immune thrombocytopenia
Thrombotic thrombocytopenic purpura
Disseminated intravascular coagulation
Acute leukemia
Microcytic anemia: Pathology review
Macrocytic anemia: Pathology review
Abscesses
Asthma
Pemphigus vulgaris
Graves disease
Systemic lupus erythematosus
Contact dermatitis
Acne vulgaris
Lichen planus
Atopic dermatitis
Psoriasis
Urticaria
Seborrhoeic dermatitis
Actinic keratosis
Bullous pemphigoid
Cellulitis
Erysipelas
Necrotizing fasciitis
Impetigo
Candida
Skin cancer
Acneiform skin disorders: Pathology review
Rotator cuff tear
Dislocated shoulder
Carpal tunnel syndrome
Ulnar claw
Unhappy triad
Patellar tendon rupture
Achilles tendon rupture
Patellofemoral pain syndrome
Sprained ankle
Meniscus tear
Anterior cruciate ligament injury
Iliotibial band syndrome
Compartment syndrome
Rhabdomyolysis
Osteoarthritis
Rheumatoid arthritis
Gout
Ankylosing spondylitis
Septic arthritis
Bursitis
Baker cyst
Polymyalgia rheumatica
Fibromyalgia
Dermatomyositis
Raynaud phenomenon
Back pain: Pathology review
Non-steroidal anti-inflammatory drugs
Osteoporosis medications
Anatomy of the cerebral cortex
Anatomy of the cerebellum
Anatomy of the brainstem
Cerebral circulation
Sleep
Intracerebral hemorrhage
Epidural hematoma
Subdural hematoma
Subarachnoid hemorrhage
Concussion and traumatic brain injury
Migraine
Tension headache
Alzheimer disease
Frontotemporal dementia
Parkinson disease
Multiple sclerosis
Adult brain tumors
Cauda equina syndrome
von Hippel-Lindau disease
Guillain-Barre syndrome
Horner syndrome
Dementia: Pathology review
Headaches: Pathology review
Cerebral vascular disease: Pathology review
Traumatic brain injury: Pathology review
Seizures: Pathology review
General anesthetics
Local anesthetics
Anatomy clinical correlates: Other abdominal organs
Anatomy of the abdominal viscera: Kidneys, ureters and suprarenal glands
Anatomy of the urinary organs of the pelvis
Renin-angiotensin-aldosterone system
Acid-base map and compensatory mechanisms
Kidney stones
Hydronephrosis
Acute pyelonephritis
Renal artery stenosis
Urinary incontinence
Lower urinary tract infection
Electrolyte disturbances: Pathology review
Urinary incontinence: Pathology review
Kidney stones: Pathology review
Loop diuretics
ACE inhibitors, ARBs and direct renin inhibitors
Potassium sparing diuretics
Osmotic diuretics
Carbonic anhydrase inhibitors
Thiazide and thiazide-like diuretics
Endometriosis
Cervical cancer
Prostate disorders and cancer: Pathology review
Reading a chest X-ray
Upper respiratory tract infection
Sarcoidosis
Pneumonia
Lung cancer
Pneumothorax
Pulmonary embolism
Pulmonary edema
Pulmonary hypertension
Pneumonia: Pathology review
Deep vein thrombosis and pulmonary embolism: Pathology review
Pleural effusion, pneumothorax, hemothorax and atelectasis: Pathology review
Eczematous rashes: Clinical
Syncope: Clinical
Leg ulcers: Clinical
Aortic aneurysms and dissections: Clinical
Heart failure: Clinical
Abdominal pain: Clinical
Appendicitis: Clinical
Peptic ulcers and stomach cancer: Clinical
Diverticular disease: Clinical
Pancreatitis: Clinical
Hernias: Clinical
Abdominal trauma: Clinical
Gallbladder disorders: Clinical
Gastrointestinal bleeding: Clinical
Bowel obstruction: Clinical
Fever of unknown origin: Clinical
Kidney stones: Clinical
Headaches: Clinical
Lower back pain: Clinical
Pneumothorax: Clinical
Joint pain: Clinical
Pediatric ear, nose, and throat conditions: Clinical
Pediatric constipation: Clinical
Pediatric vomiting: Clinical
Pediatric infectious rashes: Clinical
Pediatric bone and joint infections: Clinical
Medication overdoses and toxicities: Pathology review
Dizziness and vertigo: Clinical
Substance misuse and addiction: Clinical
Esophageal surgical conditions: Clinical
Preoperative evaluation: Clinical
Postoperative evaluation: Clinical
Pregnancy
Routine prenatal care: Clinical
Hypertensive disorders of pregnancy: Clinical
Antepartum hemorrhage: Clinical
Premature rupture of membranes: Clinical
Stages of labor
Abnormal labor: Clinical
Vaginal versus cesarean delivery: Clinical
Postpartum hemorrhage: Clinical
Gestational trophoblastic disease: Clinical
Breastfeeding

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)