Hem Onc Flashcards

1
Q

where are blood cells formed?

A

bone marrow

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2
Q

what is plasma made of?

A

water
ions
proteins
nutrients
waste
gasses

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3
Q

what is the lifespan of a platelet?

A

8-10 days

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4
Q

what is the lifespan of a RBC?

A

90 days

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5
Q

what percent of blood is made up of platelets and WBCs?

A

1%

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6
Q

what percent of the blood is RBCs?

A

about 44%

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7
Q

where are blood cells made in children?

A

mostly long bones

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8
Q

where are blood cells made in adults?

A

flat bones
pelvis, sternum, spine, skull

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9
Q

what is a CBC?

A

evaluation of blood cell types present
WBC count, hemoglobin, hematocrit, platelets

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10
Q

what is a CBC with differential?

A

includes types of WBCs present
neutrophils, lymphocytes, monocytes, eosinophils, basophils

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11
Q

what does it mean if eosinophils are elevated?

A

allergic reaction

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12
Q

what does it mean if lymphocytes are elevated?

A

viral infection

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13
Q

what do eosinophils fight?

A

parasitic infection

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14
Q

what do neutrophils do?

A

help with phagocytosis

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15
Q

what do basophils do?

A

inflammatory and allergic reactions

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16
Q

what do lymphocytes do?

A

produce specific immune response
B, T, NK cells

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17
Q

what do monocytes do?

A

fight bacteria, viruses, fungi

18
Q

what is hematocrit?

A

% of circulating RBCs

19
Q

fetal hemoglobin

A

has higher binding affinity than adult hemoglobin

20
Q

what is anemia?

A

inadequate number of RBCs for body requirements

21
Q

symptoms of anemia

A

weakness
pallor
fatigue
poor concentration
cool skin
tachycardia
hypotension

22
Q

what occurs in sickle cell disease?

A

healthy RBCs are destroyed, have sickle shape that can cause obstruction of blood flow

23
Q

cause of sickle cell disease

A

autosomal recessive
8% of african americans have recessive trait

24
Q

what is a sickle cell pain crisis?

A

tangled sickle cells cause obstruction and inflammation

microvascular occlusion causes local hypoxia, ischemia, and infarct

25
when does sickle cell disease manifest, and why?
late in infancy because fetal hemoglobin prevents sickling of RBCs
26
treating sickle cell disease
hydroxyurea rest hydration electrolyte replacement pain control
27
what is beta thalassemia?
causes microcytic anemia
28
manifestations of untreated beta thalassemia
poor growth skeletal abnormalities jaundice
29
what is iron overload?
iron deposited in heart, liver, endocrine glands can cause hypogonadism and DM from endocrinopathies
30
splenomegaly
occurs in symptomatic thalassemia can worsen anemia can cause neutropenia and thrombocytopenia
31
why are thromboembolic events common with beta thalassemia?
they may develop hypercoagulable state, common to develop after splenectomy
32
what is MCV?
mean corpuscular volume measures average size of RBCs
33
lab values to differentiate between thalassemia and IDA
ferritin is normal in thalassemia and low in IDA
34
petechiae and purpura vs rash
rash will blanch bleeding under skin will not blanch
35
what is IgA vasculitis?
inflammation causes capillaries to be porous and present with purpura
36
what is the leading cause of death by disease in children?
cancer
37
what is the overall survival rate of childhood cancer?
about 90%
38
most common types of cancer in children
leukemia CNS tumors lymphomas neuroblastoma
39
pathophysiology of leukemia
abnormal regulation and maturation of blood cells pancytopenia = immature cells in bone marrow compete with normal cells for nutrients and space to grow
40
signs and symptoms of leukemia
bleeding, bruising hepatosplenomegaly, lymphadenomegaly fatigue, pallor, fever bone pain weight loss
41
what is considered standard risk for ALL?
age 1-9 WBC<50,000