Heme First Aid Flashcards

1
Q

WBC Differential

A

N L M E B

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2
Q

increased immature neutrophils/band cells

A

increased myeloid production

  • bacterial infection
  • CML
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3
Q

Causes of Eosinophilia

A
neoplastic
asthma
allergic processes
CVD
parasites
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4
Q

B lymphocyte

A

humoral immune

bone marrow

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5
Q

T lymphocyte

A

stem cells in bone marrow, matures in thymus

cellular immune response

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6
Q

cytotoxic T cells

A

Cd8

recognized MHC I

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7
Q

Helper T cells

A

express CD4

recognize MHC II

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8
Q

Acanthocyte/spur cell

A

liver disease

abetalipoproteinemia

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9
Q

Basophilic stippling

A

thalassemias
anemia of chronic disease
lead poisoning

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10
Q

bite cell

A

G6PD def

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11
Q

elliptocyte

A

hereditary elliptocytosis

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12
Q

Macro-ovalocyte

A

megoblastic anemia

marrow failure

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13
Q

ringed sideroblasts

A

sideroblastic anemia

excess iron in mitochondria

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14
Q

schistocyte/helmet cell

A

DIC
TTP
HUS
traumatic hemolysis

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15
Q

spherocyte

A

hereditary spherocytosis

autoimmune hemolysis

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16
Q

tear drop cell

A

bone marrow infiltration (myelofibrosis)

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17
Q

target cell

A

HbC disease
Asplenia
Liver disease
thalassemia

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18
Q

Heinz body

A

G6PD def

heinz-body like inclusions with alpha thalassemia

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19
Q

Howell-Jolly bodies

A

functional hyposplenia or asplenia

mothball ingestion/napthalene

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20
Q

microcytic, hypochromic anemias

A

iron def
alpha thalassemia, beta thal
lead poisoning
sideroblastic

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21
Q

macrocytic anemia

A

foltae, b12 def

nonmegaloblastic macrocytic anemias

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22
Q

normocytic, normochromic anemias

A

intravascular, extravascular hemolysis
ACD
aplastic anemia
CKD

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23
Q

intravascular hemolysis

A

increased LDH

hemoglobin in urine

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24
Q

extravascular hemolysis

A

increase LDH plus increased UCB (jaundice!)

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25
Paroxysmal Nocturnal Hemoglobinuria symptoms
hemolytic anemia, pancytopenia, venous thrombosis
26
PN Hemoglobinuria cause
increased complement mediated RBC lysis | loss of GPI linked proteins (CD 55/59)
27
Labs for PN Hemoglobinuria
CD 55/ 59
28
Treatment for PN Hemoglobinuria
eculizumab
29
Hereditary Spherocytosis treatment
splenectomy
30
Hereditary Spherocytosis Cause
red cell membrane instability | defect in ankyrin or spectrin
31
G6PD exacerbated by
sulfa drugs infections fava beans
32
G6PD genetics
X linked decreased glutathione Heinze bodies + bite cells
33
Pyruvate kinase definency
hemolytic anemia in new born
34
autosplenectomy
Howell-Jolly bodies | sickle cell
35
Sickle Cell treatment
hydroxyurea (increases HbF) | BMT
36
Warm agglutinin
IgG | often seen with SLE, CLL, alpha-methyldopa
37
Cold Agglutinin
IgM | seen in CLL, mono, mycoplasma pneuomnia
38
Microangiopathic anemia
schistocytes
39
weird causes of microangiopathic anemia
malignant htn | sle
40
Iron Def Labs
decreasd Iron increased TIBC/transferrin decreased ferritin decreased transferrin saturation (serum iron/TIBC)
41
transferrin saturation
iron/TIBC
42
Chronic disease labs
decreased iron decreased transferrin/TIBC increased ferritin
43
Hemochromatosis labs
increased iron decreased transferrin increased ferritin increased transferrin saturation
44
Pregnancy/OCP lab values
increased transferrin/TIBC | decreased transferrin saturation
45
transferrin
transport iron in blood
46
ferritin
primary iron storage protein
47
Hemophilia A
``` def of VIII increase PTT ```
48
Hemophilia B
``` def of IX increase PTT ```
49
Vit K def
decrease synthesis of 2,7,9,10, protein C and S
50
Hodgkin's Lymphoma
associated with EBV Reed-Sternberg Cells B signs/symptoms localized nodes
51
Non-Hodgkin's Lymphoma
multiple, non contiguous nodes mostly involving B cells associations with HIV and immunnosuppresion
52
Reed-Sternberg Cells
CD 30+, CD 15+ B cells
53
plasma cells with clock face
Multiple Myeloma
54
ALL
<15 years often mediastinal mass increased lymphoblasts
55
Hair Cell Leukemia
B cell tumor in elderly | TRAP positive
56
Hairy Cell Leukemia treatment
cladribine | adenosine analog
57
AML
Auer rods older onset DIC common
58
t(9:22)
CML philadelphia chromosome bcr-abl
59
t(8:14)
Burkitt's lymphoma | c-myc activation
60
t(11:14)
cyclin D1 activation | mantle cell lymphoma
61
T(14:18)
follicular lymphomas | bcl-2 activation
62
Polycytehmia vera
Jak2 mutation | increased, RBC, WBC, platelets
63
JAK 2 mutation
polycytehmia vera
64
deficient alpha-aminolevulinic acid
lead posioning
65
symptoms of lead poisoning
mental deterioation, sideroblastic anemia
66
anti-GpIIB/IIIa antibodies
ITP
67
increased megakarocytes
ITP
68
ADAMTS 13
vWF metalloprotease | TTP
69
ITP, TPP lab values
increased BT | normal PT, PTT
70
polycythemia symptoms
itching after shower (increased histamine) ruddy skin palpable spleen
71
conseuqence of HIT
deep vein and arterial thrombosis
72
Hereditary Angioedema
swelling of eyelids and lips | decrease C1 esterase inhibitor
73
Heparin
anti-coagulant | cofactor for activation of anti-thrombin
74
Warfarin
chronic anti-coag | interferes with synthesis and carboxylation of vit K dependent clotting factors
75
Heparin monitoring
PTT (intrinsic)
76
Warfarin monitoring
PT/INR (extrinsic)
77
Warfarin overdose treatment
IV vitamin K and fresh frozen plasma
78
ribavirin SE
hemolytic anemia
79
Hodgkin's lymphoma treatment
Bleomycin
80
Pacitaxel use
ovarian and breast carcinomas
81
A blood Group
A antigen on RBC | anti-B antibody
82
B blood Group
B antigen | anti-A antibody
83
AB blood group
A, B antigens no antibodies universal recipient of RBC universal donor of plasma
84
O blood group
Anti-A and Anti-B antibodies universial donor of RBCs universal recipient of plasma
85
HbH
deletion of three alpha genes | excess Beta globulin forms Beta-4 (HbH)
86
Plummer-Vinson syndrome
iron def anemia esophageal webs atrophci glossitis