Exam 2 material Flashcards

(70 cards)

0
Q

Hypersensitivity Type II

A

Tissue specific/antibody mediated, B-cells. Prod. of IgG & IgM, typically in blood transfusions. Antibody finds antigen and forms complex in the tissue. Common in post-strep infection
Outcomes: inflammation, auto-antibody production (Myasenthia Gravis, Graves Disease)

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1
Q

Hypersensitivity Type I

A

IgE-meditated, B-cells. Normal allergic response, IgE normally low (except in Atopic indiv.)
Symptoms: most due to vasoactive amines, itching, edema, runny nose, red eyes
Examples: anaphylaxis, food/environ. allergy, wasp/bee venom, drugs

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2
Q

Hypersensitivity Type III

A

Immune-complex mediated, B-cells. Prod. of IgG & IgM. Antibody-antigen complex circulates, get stuck in organ that filters
Often found in organs that filter (kidney->glomerulonephritis, joints->reactive arthritis)

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3
Q

Hypersensitivity Type IV

A

Cell mediated, T-cells (CD4 or CD8). CD4 results in slower death than CD8. Chronic conditions, reaction takes more time
Ex: Crohn’s, dermatitis, MS, DM Type I, Hashimoto disease, RA, Celiac disease, Transplant rejection

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4
Q

Transplant Rejection

A

Type IV hypersensitivity
Can be direct (CD8) or indirect (CD4) recognition
Use immunosuppressant drugs

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5
Q

Autoimmune diseases

A
Systemic Lupus erythermatosus: type III (cutaneous, drug, fetal)
Rheumatoid Arthritis (RA): Type IV, might be antigen in collagen II
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6
Q

B-Cell Immune deficiencies

A

X-linked agammaglobulinemia (Bruton disease): B-cells cannot differentiate to make functional antibodies, sex-linked
IgA deficiency: most common primary deficiency, trouble making IgA, so infections where IgA normally found

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7
Q

T-cell deficiencies

A

DiGeorge Syndrome: partial/complete lack of thymus, so no mature T-cells/low levels or T-cells. Difficulty fighting infections. Peds-thymus transplant

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8
Q

Severe Combined immune deficiency disease

A

SCIDS, ADA deficiency
no B or T cells
highly susceptible to infectious agents
Bubble boy disease

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9
Q

Glial cells in both systems

A

CNS: Microglial, astrocytes, ependymal, oligodendrocytes
PNS: Satellite, Schwann

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10
Q

Broca’s area

A

ability to form speech (motor)

know what they want to say, cannot find right word

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11
Q

Wernicke’s area

A

posterior
ability to understand speech (sensory)
speaks “normal”, but doesn’t know what they’re saying

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12
Q

Cerebral edema causes

A

Cytotoxic: usually insult from toxin, acute cerebral ischemia, glial cells enlarge
Vasogenic: endothelial cells too leaky, fluid leaks out, high altitude cerebral edema

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13
Q

Hydrocephalus

A

Not draining CSF fast enough, or making too much

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14
Q

Brain herniation

A

increase in intracranial pressure
possible from edema, hydrocephalus, trauma
lead to infarct b/c no blood to pressurized cavity
Types: subfalcine (relocates midline), Uncinate (pushes into stem), Tonsilar (at back of throat on brain stem)

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15
Q

Cerebrovascular disease (stroke)

A

abnormality, blood vessel problem
3 processes can cause:
Thrombotic occlusion (vessel inner lining simulates a clot, localized)
Embolic occlusion (disease in vessel decreases opening, clot stick here, localized)
Vessel rupture (leads to hemorrhage)

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16
Q

Cerebral ischemia (global)

A

blood flow compromized, widespread ischemia and hypoxic injury
brain cells die in 4-6 minutes
unconscious in under 10 seconds
Mild: confusion, recover
Severe: neuronal death, death, vegetative state

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17
Q

Cerebral ischemia (focal/local)

A

usually arterial occlusion
leads to infarction
may not lose fxn if focal, because other parts of the brain can profuse
permanent compromise
TIA (transient ischemic attacks): temporary blood loss, reversible

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18
Q

Acute brain trauma

A

insult to brain
Blunt (common) or open
Coup: brain strikes anterior side
Contrecoup: strikes anterior side, then recoils to posterior
DAI (diffuse aconal injury): shaken baby syndrome
Focal: concussion, contusion, hematoma

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19
Q

Meningitis

A

infection of dura and arachnoid mater
viral, bacterial, fungal
Symptoms: photophobia, neck stiffness, irritability

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20
Q

Creutzfeldt-Jakob disease (CJD)

A

mutation or prion

rapid dementia

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21
Q

Multiple Sclerosis

A

Type IV hypersensitivity

demyelinating autoimmune disease

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22
Q

Alzheimers

A

common form of dementia
beta-amyloid plaques and neurofibrillary tangles (plaque/scar tissue in brain)
first appears as disorder of higher brain functions (forgetfulness)

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23
Q

Parkinson’s disease

A

depigmentation of substantia nigra (loss of dopamine production, which normally stops unwanted tremors)
don’t understand what causes
sometimes in people with lots of brain injuries

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24
Uncinate vasciculous
connection between Broca's and Wernicke's areas, important for speech
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Neurobiotaxis
movement of neuron to make connections | brain wiring determines type of person
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Organizations of brain function
Caudal to rostral (head to tail): higher up=higher order, lower=more basal fxn Sensory-motor dichotomy (back to front) Laterality of function (right to left): which hemisphere mediates which functions
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Important brain regions
posterior: sensory, anterior: motor temporal lobe: linguistic. cerebellum: everything Frontal lobes: programming, personality, behavior, reasoning, attention, concentration Hippocampus: long term memory, easily injured Amygdala: tells hippocampus what to learn/memorize
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Amnesia
Wernickes-Korsakoff syndrome: severe alcohol intake Neoplasms: tumors on hippocampus Herpes encephalitis: attack hippocampus
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Neoplasm
new growth
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Dysplasia
malformation
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-oma
tumor
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-sarcoma
connective tissue from mesoderm
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-emia
blood
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-carcinoma
superficial, epithelial cells
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Carcinoma in situ (CIS)
pre-cancer before it's metastasized, noninvasive
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Adenocarcinoma
epithelium of glandular tissue (prostrate)
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Leukemia
cancer of blood or bone marrow
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Lymphoma
cancer within lymphatics
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Rhabdomyosarcoma
benign tumor in skeletal muscle, has anaplastic and pleomorphic cells
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Anaplasia
loss of organization, nucleus size increase
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Pleomorphic
abnormal size and shape
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Carcinogen
anything that can cause DNA mutation
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Characteristics of a benign neoplasm
``` slow growth/low mitosis well-defined border noninvasive cells well-differentiated no metastasis not called cancer, could be pre-cancer ```
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Characteristics of a malignant neoplasm
``` rapid growth/high motosis undefined border invade local tissues poor differentiation, looks different from surrounding tissue possibility of metastasis called cancer ```
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Telomerase
lengthens telomeres that naturally shorten as DNA is replicated, loses efficiency with age cancer cells can hijak function and divide limitlessly
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Characteristics of a cancer cell
``` self-sufficient in growth signals insensitive to anti-growth signals tissue invasion/metastasis limitless reproductive potential sustained angiogenesis evading apoptosis ```
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p53
tumor-suppressing gene upregulated with DNA damage to repair or signal apoptosis if mutated, cells can become cancerous with DNA mutation
48
Retinoblastoma (Rb)
allows for/blocks transcription based on phosphorylated (w/ P=allowed, w/out=prevent
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Tumor markers
Her2, PSA
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Causes for carcinogens
``` chronic inflammation (ulcerative colitis->colon cancer) infection (HPV->cervical cancer) Environmental factors (UV radiation, air pollution) ```
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Endocrine system
secretes hormones directly into bloodstread
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Exocrine
secretes proteins/hormones into ducts that open to outside environment
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Paracrine
local signaling
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Autocrine
"self" signaling
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Classes of hormones
Peptides: fragments of proteins Steroids: derived from cholesterol Monoamines: derived from tyrosine Eicosanoids: derived from arachadonic acis
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Synergistic hormone interaction
combined effects of two hormones greater than either individually or sum
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Antagonistic hormone interaction
two hormones with opposing actions (insulin and glucagon)
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Permissive hormone interaction
one hormone enhances tissue's response to second hormone (estrogen & progesterone)
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Hypothalamus hormones
located beneath thalamus | TRH, GnRH, CRH, GHRH/GHIG, PRF/PIF
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Anterior pituitary hormones
one of the major organs in endocrine system | TSH, LH, FSH, ACTH, GH
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Posterior pitutary hormones
ADH, oxytocin
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Types of adenomas
Functional: tumor producing hormone, but not correct amounts Silent: hormone manufactured, but non-functional Hormone negative: no hormone produced or detected
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Hyperpituitarism
could be caused by prolactinoma (most common functional adenoma) high levels of prolactin Women: galactorrhea (spont. milk), amenorrhea (no period) Men: oligospermia, reduced libido, ED Other effects: optic chiasm or cranial nerve impingement, gigantism (childhood), acromegaly (adulthood)
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Hypopitutarism
caused by: infarction, TBI, infection, surgical damace Signs/symptoms depend on hormone Sheehan syndrome: pituitary normally increases in size during pregnancy, but can have postpartum hemorrhage during childbirth
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Hyperthyroidism
over-active thyroid, thyrotoxicosis Primary: commonly caused by Graves disease, could be toxic goiter or functional adenoma Secondary: hypersecretion of TSH from anterior pituitary
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Hypothyroidism
under-active thyroid congenital hypothyroidism: cretinism Primary: autoimmunity, thyroiditis, endemic goiter, antithyroid drugs. Hashimoto disease. Diagnose by levels of TSH (normal=thyroid, low, then AP) Secondary: congential abnormality, loss of tissue after hyper treatment, cretinism
67
Diabetes insipidus
"syphen without taste" loss of fluid into urine Symptoms: polydipsea (thirst), polyurea (excessive urine), hypernutremia (excessive sodium in blood) Types: neurogenic (common, PP neurons not enough ADH), nephrohenic (kidney unresponsive to levels of ADH, end-stage renal failure
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Diabetes Mellitus
"siphoning sweet like honey" Type I: inability to produce appropriate amounts of insulin Type II: inability to respond to insulin, beta cell dysfunction Symptoms: polydipsia, polyuria, polyphagia, hyperglycemia, weight loos (I), weight gain (II), ketoacidosis (ketones for fuel, pH dec.), hyperinsulinema (II), hyper tension, fatigue, parasthesias (tingling), infections
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DM treatments
I: insulin injection II: various drugs