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pernicious/megaloblastic anemia + treatment
megaloblasts
vitamin B12 deficiency
oral supplements and b12 injections
what is the most common cause of vitamin b12
etiology
autoimmune reaction, chronic gastritis, inflammatory
sickle cell anemia
recessive inherited characteristic
abnormal hemoglobin formation (deoxygenated)
disk→crescent/sickle shape when O2 levels are low = less life span
cell membrane is damaged leading to hemolysis
problem w/ sickel cell anemia
obstruction of small blood vessels by RBC’s. causing thrombus formation (blood clots), causing infarction → necrosis
treatment for sickle cell
hydroxyurea (oral chemo)
b9/folic acid
bone marrow transplant
leukemia
leukocyte are undifferentiated = immature
multiply uncontrollably in bone marrow which causes infiltration in organs
acute leukemia
high proportion of immature non-functional cells in bone marrow
sudden
primarily in children & young adults
chronic leukemia
higher proportion of mature cells but may have lower functionality
mild signs, better prognosis
older people
multiple myeloma
neoplastic disease that causes increased production of malignant plasma cells that replace and erode bone marrow
tumours, loss of bone, bone pain
hodgkin lymphoma vs non-hodgkin lymphoma
hodgkin - single lymph node then spreads, defective t lymphocytes with less lymphocytes
non - widespread with multiple nodes, b-lymphocytes
UTI
urinary tract infection
most ascending
e-coli
cystitis
inflammation of the bladder
capacity reduced
pain , pain while peeing, peeing at night, clodu w odour
pyelonephritis
inflammation of the renal pelvis and medulla
may involve 1 or both kidneys
recurrency can cause failure and necrosis
dull aching pain, fever
antibiotics, cranberry juice
glomeulonephirtis / acute post streptococcal
beta hemolytic streptococcal (GAS) infection
acute/chronic renal failure
scarring of kidneys
urolithiasis
concentrated urine (salt)
accumulates causing infection
and immobility, causing nephrosis
nephrosis
swelling of one or both kidneys caused by a buildup of urine that cannot properly drain into the bladder
hydronephrosis
secondary problem
urine filled dilatation of renal pelvis
atrophy of kidney due to urinary outflow obstruction → infection —> necrosis → failure
renal cell carcinoma
hypernephroma
PRIMARY tumour
painless, metastasized
wilms tumour (nephroblastoma)
very common in children 3-5 years
Adult Polycystic Kidney Disease
genetic
fluid filled cysts
bilateral, causing chronic renal failure
acute vs chronic failure
acute - sudden, reversible
chronic - gradual loss, irreversible
no pee (auria), less urine (oliguria), nitrogenous waste
hiatus hernia
part of the stomach is elevated and protrudes through opening in diaphragm into thoracic cavity
shorter esophagus, pressure in abdomen, weakness of diaphragm
sliding vs rolling hernia
sliding - stomach & GE junction protrudes
rolling - fundus of stomach moves up
peptic ulcer
exposed to acid due to pepsin secretion
hemmorhage
gallstones
masses of solid or calculi in bile, cholestrol, or bilirubin (pigment)
jaundice
yellowing skin resulting from high levels of bilirubin in blood
pre vs intra vs post heptatuc jaundice (type of bilirubin?)
pre - unconjugated bilirubin
intra - bilirubin of both types
post - conjugated bilirubin
hepatitis
inflation of liver
hepatitis B
untreated can lead to long-term mild infection, cirrhosis, or hepatic cancer
cirrhosis
alcohol, cronic hepatitis
diverticular disease
sigmoid colon
herniation
cryptorchidism
undescended testes
m/c in premature & low birth weight infants’
inferitility and malignancy
hydrocele
accumulation of excessive fluid
cystic mass in scrotum
varicocele
dilation of veins in the pampiniform plexus of veins (veins draining the testes) on left side
BPH benign prostatic hypertrophy/hyperplasia
age related common diseasw, non malignant enlargement of prostate gland
compression of urethra which can cause dribbling and uti’s
testicular carcinoma
germ cell tumours, rare
enlargement of testicles, hard masses
diabetes mellitus
deficit of insulin secretion by islets of langerhans or insulin esistance
abnormal metabolism of macronolecules
high glucose levels
3 p’s of diabetes
polyuria, polydipsia, polyphagia
diabetes insipidus
deficit of ADPH/vasopressin
unable to concentrate the urine
diabetes insipidus 2 types
neurogenic/central - synthesis or release of ADH
nephrogenic - do not respond to ADH
goiter
enlargement of thyroid gland
hypo/hyper
low iodine excessive stim of TSH
hypothyroidism - hashimoto’s thyroiditis
destructuve autoimmune disorder
hypothyroidism - myxedema
severe hypothydoism in adulys
hypothyroidism - cretinism
in children
adrenal - pheochromocytoma
benign tumour of the medulla
secretes epinephrine and norepinephrine
adrenal - cushing’s syndrome
hypercortisolism
adrenal - addison’s disease
deficit of glucocorticoids, mineralocorticoids, androgens
hypoglycemia
endometriosis
endometrial tissue outside uterus
endometrioma
cyst filled with old blood in ovary - chocolate cyst
leiomyoma (fibroids)
begnign tumours of smooth muscle, common, asymptomic if small
ovarian cysts
fluid filled sacs in ovaries, benign, pain
Polycystic Ovarian Disease
large ovaries with multiple cystsm causing abnormalities in hormones, ovulation doesnt occur
cervical carcinoma
STD’s, early sx, asymptomatic
Transient Ischemic Attack
mini stroke
temporary localized reduction of blood flow in brain
recovery within 24 hours
warn of potential stroke/CVA
CVA/stroke
infarction (ncerosis by lack of o2) of brain tissue resulting from lack of blood
total occlusion of cerebral blood vessels
3 types of cva/stroke
atheroma - gradual
embolus - sudden (due to tumour, air, infection)
hemmorhage - sudden
Cerebral Aneurysm
dilation in artery, multiple (weak→bulge→compression of structures)
mostlt iccur at circle of willis
what does cerebral aneurysm rupture into
the subarachnoid space & csf → high pressure in skull
loss of vision, consciousness
meningitis
inflammation of meninges of brain and spinal cord
microbes (e. coli) reach brain via blood, inflammatory response
encephalitis
infection of the parenchymal or connective tissue in the brain or spinal cord
west nile
herpes
ticks
inflammation→necrosis→loss of function
contusion
bruising of brain tissue with rupture of small blood vessels
compound fractures
brain tissue exposed to environment, risk of infection
depressed skull fractures
displacement of piece of bone below skull
pressing into brain tissue
increases ICP
basilar fracture
leaking of CSF through ears and nose
countrecoup injury
injury occurring on the side opposite the initial head impact by bouncing off skull
hematoma
collection of blood in tissue from ruptured blood vessels
hydrocephalus
water on the brain
CSF accumulating compressing brain tissue and blood vessels
enlarged brain
noncimmunicating hydrocephalus
flow of CSF blocked
communicating hydrocephalus
absorption of CSF impaired
spina bifida
neural tube defects
multifactorial
spina bifida occulta
spinal process does not fuse
spina bifida - meningocele
herniation of the meninges & CSF
spina bifida - myelomeningocele
most serious,
herniation of spinal cord, meninges, csf
neuro impairment
multiple sclerosis
progressive demyelination of neyrons of the brain, spinal cord, and cranial nerves
forms plaques
parkinsons disease
degenerative disease
affects motor loss due to loss of neurons in basal nuclei
low dipamine secretion