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hematopoiesis
process of blood formation
where does hematopoiesis occur?
primarily in bone marrow
what stimulates rbc production
hypoxemia
blood loss
what is necessary for development of rbcs? (4)
cytokines
iron
vitamin B12
folate
what occurs with hemoglobin production when iron is low
low iron = less hemoglobin = less oxygen carrying potential
anemia causes
blood loss
impaired rbc production
increased destruction of rbc
what is mean corpuscular volume
indicates the average size of a person’s rbc
what is mean corpuscular hemoglobin
measures the average amount of hemoglobin within a rbc
normal size
normocytic
normal color
normochromic
large size
macrocytic
small size
microcytic
pale color
hypochromic
normocytic, normochromic anemia
caused by:
acute blood loss
hemolysis
chronic renal disease
cancer
diabetes
aplastic anemia
macrocytic, normochromic anemia
normal hgb as rbcs are not pale, become big as there is a lack of vit B12 (no dna synthesis, cells not dividing)
caused by:
B12 deficiency
folate deficiency
liver disease
microcytic, hypochromic anemia
caused by:
iron deficiency anemia
thalassemia
lead poisoning
aplastic anemia
a condition where bone marrow stops making enough new blood cells
thalassemia
genetic blood disorder where the body makes abnormal hemoglobin
iron deficiency anemia
results when there is inadequate iron supply for hemoglobin production
characterized by small, pale rbcs
what populations are iron deficiency anemia most common in?
young children (<2)
women in reproductive years
diets that are not nutritionally adequate
signs and symptoms of iron deficiency anemia
pale skin + mucous membranes
fatigue / lethargy
depression, muscle aches
dyspnea, tachycardia
brittle, spoon-shaped nails (koilonychia)
decreased appetite, pica
sickle cell disease
an inherited blood disorder where the body produces abnormal hemoglobin called “HbS”
under low oxygen conditions (cold exposure, dehydration, infection, etc) rbcs change to a rigid, sickle shape that obstruct capillaries and become sticky
this causes a vasocclusive crisis
sickle cell crisis
tissue ischemia and pain
with reoxygenation cells return to normal
lifespan of sickled cells
10-20 days
inheritence of sickle cell disease
both parents must be a carrier
most carriers are asymptomatic
preventon of sickle cell crisis
avoid hypoxia
encourage hydration
avoid cold exposure, infection, stress
vaccination
prophylactic penicillin in children until age 5
disease modifying therapies for sickle cell anemia
hydroxyurea: increases fetal hemoglobin, reduces sickling and pain crisis
bone marrow transplant
triggers for sickle cell crisis
infection
dehydration
stress
cold exposure
leukemia
cancer of the blood cells that usually starts in the bone marrow and travels through the blood stream
overproduction of blast cells. immature blood cells are not differentiating into rbcs, platelets, neutrophils, etc.
types of leukemia
acute lymphoblastic leukemia (ALL)
acute myelogenous leukemia (AML)
chronic (CLL and CML)
difference = whether its the lymphoid or the myeloid stem cells becoming malignant
signs and symptoms of leukemia
fever
bleeding
lethargy
anorexia
petechia
diagnosis of leukemia
bone marrow aspiration is the only way to fully diagnose leukemia
expected abnormal labs for leukemia
low platelets
low hemoglobin
elevated wbcs
presence of blast cells
risk levels for ALL (5)
standard risk:
child between ages of 1 and 10
when dx, had less than 50,000 wbc
no blast cells in csf
high risk:
age of less than 1 or older than 10 at time of dx (rapid times of growth)
when dx, more than 50,000 wbcs
leukemic cells in csf
testicular involvement
if steroids were given before dx
how long is treatment for ALL?
2-3 years
febrile neutropenia
abnormally low number of neutrophils
fever greater than 38.3 c or greater than 38 for more than 1 hour
medical emergency
lymphoma
the uncontrolled growth of abnormal lymphocytes
can oringate in any part of the lymphatic system (lymph nodes, spleen, etc)
cancerous lymphocytes can travel through the blood and spread to many parts of the body
hodgkin’s lymphoma
B lymphocytes only
more localized
B symptoms common
confined mostly to lymph nodes
characterized by reed-sternberg cells
causes of lymphoma
epstein-barr virus
genetic predisposition
exposure to toxins
HIV
non-hodgkin’s lymphoma
B lymphocytes and T or natural killer lymphocytes
more widespread
B symptoms uncommon
extranodal involvement common (tumors outside lymph nodes)
B symptoms lymphoma
fever
night sweats
weight loss
lymphoma symptoms
enlarged lymph node
weight loss
fatigue
weakness
fever and chills
tachycardia
night sweats
alcohol intolerance
diagnosis of lymphoma
microcytic anemia
neutrophil leukocytosis
increased platelets
lymph node biopsy
bone marrow biopsy
CT or MRI for staging
lymphoma staging
stage I: involvement of single lymph node
stage II: involvement of 2 or more lymph nodes above diaphragm
stage III: lymph node involvement above and below diaphragm
stage IV: involvement outside the lymph nodes
treatment for lymphoma
ABVD regimen - doxirubicin (adriamycin), bleomycin, vinblastine, dacarbazine
stem cell transplant
tumor lysis syndrome
oncological emergency
rapid destruction of tumor cells and tumor contents get released into bloodstream
can cause hyperkalemia, hyperuricemia, hyperphosphatemia, and hypocalcemia
symptoms of tumor lysis syndrome
nausea
vomiting
diarrhea
muscle cramps + twitches
confusion
seizures