Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
74 Cards in this Set
- Front
- Back
Hypoxia/ischemic injury to the brain is characterized by what?
|
Characterized by loss of ribonucleoproteins and denaturation of cytoskeletal proteins, resulting in cytoplasmic eosinophilia (red neurons), observed in hematoxylin and eosin stained sections
|
|
How do astrocytes react to brain injury?
|
React by producing a dense network of cytoplasmic processes surrounding the area of injury. This is somewhat analogous to a fibrous scar occurring elsewhere in the body, and is known as reactive gliosis
|
|
These are major supporting cells of the brain
|
Astrocytes
|
|
Demyelinating disorders, such as MS, are caused by damage to what cells?
|
Oligodendrocytes
|
|
These are cuboidal cells that line the ventricles
|
Ependymal
|
|
Microglia
|
- Derived from circulating monocytes
- Serve as APC in inflammatory conditions - Act as scavengers during tissue necrosis |
|
Cells with large, foamy cytoplasm are called what?
|
Glitter cells
|
|
T/F Brain herniations are caused by intracranial pressure from low to high pressure compartments
|
False, high to low
|
|
These disorders cause increased intracranial imbalances (3)
|
1) Cerebral edema
2) Brain herniations 3) Hydrocephalus |
|
Cerebral edema and its 2 types
|
- Increase in water content within the brain parenchyma
- Types (vasogenic, cytotoxic) |
|
Herniation and 3 types
|
- Brain swelling results in displacement of brain tissue from one intracranial compartment into another
- Types (transtentorial or uncal, cingulate and cerebellar tonsillar) |
|
Hydrocephalus
|
Refers to accumulation of excess cerebrospinal fluid within the ventricular system of the brain. This can be caused by (i) decreased resorption of CSF (obstruction by a tumor or an inflammatory process) or rarely by (ii) by overproduction of CSF (tumors of the choroids plexus)
|
|
Defined as rapidly evolving, non-epileptic, neurologic deficit that lasts > 24 hrs
|
Stroke
|
|
Circumscribed destructive lesions caused by local interruption of blood flow; account for about 70-80% of all cerebrovascular accidents. Atherosclerosis is the most common cause (predisposes thrombosis or embolism). 3rd most common cause of death in US.
|
Infarct
|
|
Risk factors for infarcts
|
- Hypertension
- Smoking - Diabetes - Oral contraceptives |
|
These arteries are most commonly involved in infarcts
|
Middle cerebral arteries
|
|
Histology of infarct
|
- Eosinophilic neurons and neutrophilic infiltration appear in 24-36 hours
- Macrophages begin to infiltrate by third day - One month, softening and liquefaction result in an irregular cavity - 6 months, a smooth walled cystic cavity |
|
Hypertension is the most common underling cause of this
|
Intraparenchymal hemorrhage
|
|
Intraparenchymal hemorrhage
|
Accelerated atherosclerosis in larger and hyaline arteriolosclerosis in smaller vessels weaken the vessel walls with subsequent wall rupture and hemorrhage
|
|
Most common regions of intraparenchymal hemorrhage
|
Basal ganglia> pons> thalamus> cerebellum
|
|
Subarachnoid hemorrhage
|
Acute extravasation of blood in space between arachnoid and pia mater due to rupture of vessels in subarachnoid space. Often spontaneous (although traumatic injury may precipitate) and patients complain of “worst headache of my life”
|
|
Ruptured berry (saccular) aneurysm (of major brain arteries) is most common cause of non-traumatic what?
|
Subarachnoid hemorrhage
|
|
Subarachnoid hemorrhage come from what vessels?
|
From the branches of middle cerebral, internal carotid and the junction between the anterior cerebral and anterior communicating arteries
|
|
T/F Intraparenchymal and subarachnoid hemorrhages cannot be seen together?
|
False, they can
|
|
Four major types of vascular malformations and how they result
|
1) Arteriovenous
malformation (AVM) 2) Cavernous angioma 3) Capillary telangiectasias 4) Venous angioma * Result from abnormal angiogenesis |
|
Vascular malformations
|
They are composed of irregular collections of blood vessels of varying caliber that include arteries, veins and transitional forms. They can be associated with intraparenchymal as well as subarachnoid hemorrhage. Malformations can be an incidental finding, can cause focal neurologic deficits or can lead to fatal brain hemorrhage.
|
|
__ are the most common vascular malformations and are most likely to give rise to brain hemorrhages
|
Arteriovenous malformation (AVM)
|
|
Leading cause of death and disability, accounting for over 25% of all accidental deaths
|
Trauma
- blunt - penetrating (gun shot) |
|
Traumatic injury involving blunt force include ____, ___ and ___
|
Epidural hematoma, subdural hematoma and parenchymal injury.
|
|
Epidural hematoma
|
Arterial bleeding, frequently caused by rupture of a meningeal artery, usually as a result of skull fracture. Middle meningeal aretery is most commonly involved.
|
|
Hematoma forms in between skull bone and dura matter, with compression of the underlying brain. Patients commonly experience a ‘lucid interval’, followed by progressive loss of consciousness.
|
Epidural hematoma
|
|
T/F Menigneal arteries are intimately attached w/ skull bones and are easily torn at fracture sites
|
True
|
|
Subdural hematoma
|
Venous in origin. Caused by disruption of the bridging veins that extend from the surface of the brain to the dural sinuses. Blows to the head, vigorous shaking of head and whiplash injury may produce acute subdural hematoma
|
|
Blood collects between dura matter and arachnoid membrane
|
Subdural hematoma
|
|
Chronic subdural hematomas are associated with what and how are they caused?
|
Assoc. w/ atrophic brains (elderly) and may be caused by trivial trauma since atrophic brains have greater mobility w/i the cranium
|
|
Traumatic parenchymal injuries include (3)
|
1) Concussion
2) Contusion 3) Laceration |
|
Loss of consciousness with full recovery and no sequelae
|
Concussion
|
|
Contusion
|
A hemorrhage in the superficial brain parenchyma caused by blunt trauma. Certain regions of the brain that come in contact with the skull are prone to develop contusioinal injury, including the frontal, temporal and occipital poles
|
|
Coup lesion
|
Contusion immediately underneath the point of contact
|
|
Contrecoup lesion
|
Contusion that develops in an area away from the site of impact
|
|
Traumatic tearing of the superficial layers of brain
|
Laceration
|
|
Infectious routes
|
Different routes of entry that include hematogenous spread, direct implantation (trauma), local extension of infections (sinusitis, middle ear or dental infections) and via peripheral nerves (rabies).
|
|
___spread is the most common infectious route
|
Hematogenous
|
|
Acute Bacterial Meningitis
|
Infections resulting in inflammation of the leptomeninges and subarachnoid space
- CSF involvement is a helpful diagnosis |
|
T/F Acute purulent meningitis is cause by pyogenic bacteria while chronic leptomeningitis is caused by both bacterial and fungal organisms
|
True
|
|
Extremes of age, crowded living conditions, poor hygiene, and debilitation are risk factors
|
Acute bacterial meningitis
|
|
Clinical features of bacterial meningitis
|
Clinical features include fever, headache, stiff neck (due to meningeal irritation). Brain becomes swollen and congested. Purulence, necrotic debris and bacteria usually observed within meninges.
|
|
Usually caused by bacteria including streptococci, staphylococci and anaerobic organisms. 50% are spread from adjacent infections (dental, ear or sinus infections). Streptococcus milleri is most commonly identified microorganism.
|
Brain abscess
|
|
Clinical manifestations of brain abscess and prognosis
|
Usually solitary, can be multiple. Presents with headache, fever, neck rigidity, increased intracranial pressure and focal neurologic deficits. Extremes of age is a poor prognostic factor. Mortality is approximately 20%.
|
|
Patient presents with headache, neck stiffness, pyrexia (fever) and focal seizures. Common morphological features include perivascular lymphocytosis, microglial nodules and neuronophagia. Sometimes, viral inclusions (eg. Cowdry A and Negri bodies) can be identified.
|
Encephalitis
|
|
Encephalitis
|
Diffuse inflammation of brain parenchyma caused by a number of viral agents (HSV, HIV, cytomegalovirus and many arthropod-borne encephalitis viruses)
|
|
Tumors of the brain arise from what?
|
Cells of the brain or spinal cord and their coverings
|
|
T/F Brain tumors present clinically by their site of origin rather than their pathologic type
|
True
|
|
T/F Tumor location has nothing to do w/ its behavior?
|
False. Brain tumors have varying degrees of histological malignancy (for example the astrocytomas) but because of their critical location even benign tumors may behave in a “clinically malignant” fashion (i.e. result in fatality due to compression of vital structures)
|
|
Second most common form of brain neoplasm
|
Metastatic tumors (often from lung or breast)
|
|
Most common adult brain tumor
|
Astrocytoma
- WHO grade II, III, and IV |
|
Oligodendroglioma
|
Cells with round nuclei and perinuclear halos. Slow growing (grade II)
|
|
Ependymoma
|
Intraventricular, slow growing (grade II). Cells make perivascular pseudorosettes.
|
|
Meningioma
|
Derived from the arachnoid matter. Forms cellular whorls and psammoma bodies. 2nd most common neoplasm.
|
|
Usually cystic and occurs in the cerebellum, brain stem and optic nerve. Hairlike (piloid) processes, Rosenthal fibers and eosinophilic granular bodies are present.
|
Pilocytic astrocytoma (grade 1)
|
|
Located in the cerebellum. Cells form Homer-Wright rosettes. Usually disseminates through the CSF.
|
Medulloblastoma (grade IV)
|
|
T/F MS is more frequent in equatorial regions
|
False, temperate
|
|
Typically present in young adults, with waxing and waning of signs and symptoms, depending on the regions of brain involvement. Common manifestations include visual disturbances, speech and gait abnormalities, paresthesias and emotional disturbances
|
MS
|
|
Common site of MS plaques
|
Perivascular white matter, optic nerve, etc., but can occur anywhere in the brain or SC
|
|
Histology of MS plaques
|
Microscopically, plaques are characterized by areas of demyelination, accompanied by variable presence of perivascular lymphocytosis and infiltration by foamy macrophages
|
|
Neurodegenerative diseases can be ___ or ___, can have variable signs and symptoms including ___, movement disorders, ___, and ___
|
Sporadic, familial, dementia, tremor, rigidity
|
|
Alzheimer's Disease
|
- Most common cause of elderly dementia
- Mostly sporadic, 10% familial - Atrophic brain (loss of vol. & weight) and dilation of ventricular system - Patients present w/ progressive loss of memory and other cognitive functions that are non-reversible |
|
Diagnostic features of of Alzheimers
|
1) Senile or neuritic plaques
- aggregates of thickened, tortuous processes with a central amyloid core 2) Neurofibrillary tangles - coarse, filamentous aggregates within the cytoplasm of the neurons |
|
The hallmark of Parkinson's disease
|
Intracytoplasmic inclusion bodies known as Lewy bodies, within the pigmented neurons of the substantia nigra and locus ceruleus
|
|
The substantial nigra and locus ceruleus are involved in what disease?
|
Parkinson's
|
|
Parkinson's Disease
|
- This is caused by degeneration of the dopamine secreting pigmented neurons of the substantia nigra in the midbrain
- Unknown etiology - Most are sporadic cases in 6th decade - Mildly atrophic brain |
|
Hereditary and progressive disorder characterized by spontaneous involuntary movements called chorea and also dementia.
|
Huntington's Disease
|
|
Hallmark of Huntington's disease
|
The atrophy of the basal ganglia (caudate, putamen and sometimes globus pallidus)
|
|
Huntington's Disease
|
The onset is usually in the 4th or 5th decade. The disease is caused by mutations in the huntingtin gene, located in the short arm of chromosome 4. Microscopically, there is severe neuronal loss in the basal ganglia, accompanied by fibrillary gliosis.
|