Heme First Aid Flashcards
WBC Differential
N L M E B
increased immature neutrophils/band cells
increased myeloid production
- bacterial infection
- CML
Causes of Eosinophilia
neoplastic asthma allergic processes CVD parasites
B lymphocyte
humoral immune
bone marrow
T lymphocyte
stem cells in bone marrow, matures in thymus
cellular immune response
cytotoxic T cells
Cd8
recognized MHC I
Helper T cells
express CD4
recognize MHC II
Acanthocyte/spur cell
liver disease
abetalipoproteinemia
Basophilic stippling
thalassemias
anemia of chronic disease
lead poisoning
bite cell
G6PD def
elliptocyte
hereditary elliptocytosis
Macro-ovalocyte
megoblastic anemia
marrow failure
ringed sideroblasts
sideroblastic anemia
excess iron in mitochondria
schistocyte/helmet cell
DIC
TTP
HUS
traumatic hemolysis
spherocyte
hereditary spherocytosis
autoimmune hemolysis
tear drop cell
bone marrow infiltration (myelofibrosis)
target cell
HbC disease
Asplenia
Liver disease
thalassemia
Heinz body
G6PD def
heinz-body like inclusions with alpha thalassemia
Howell-Jolly bodies
functional hyposplenia or asplenia
mothball ingestion/napthalene
microcytic, hypochromic anemias
iron def
alpha thalassemia, beta thal
lead poisoning
sideroblastic
macrocytic anemia
foltae, b12 def
nonmegaloblastic macrocytic anemias
normocytic, normochromic anemias
intravascular, extravascular hemolysis
ACD
aplastic anemia
CKD
intravascular hemolysis
increased LDH
hemoglobin in urine
extravascular hemolysis
increase LDH plus increased UCB (jaundice!)
Paroxysmal Nocturnal Hemoglobinuria symptoms
hemolytic anemia, pancytopenia, venous thrombosis
PN Hemoglobinuria cause
increased complement mediated RBC lysis
loss of GPI linked proteins (CD 55/59)
Labs for PN Hemoglobinuria
CD 55/ 59
Treatment for PN Hemoglobinuria
eculizumab
Hereditary Spherocytosis treatment
splenectomy
Hereditary Spherocytosis Cause
red cell membrane instability
defect in ankyrin or spectrin
G6PD exacerbated by
sulfa drugs
infections
fava beans
G6PD genetics
X linked
decreased glutathione
Heinze bodies + bite cells
Pyruvate kinase definency
hemolytic anemia in new born
autosplenectomy
Howell-Jolly bodies
sickle cell
Sickle Cell treatment
hydroxyurea (increases HbF)
BMT
Warm agglutinin
IgG
often seen with SLE, CLL, alpha-methyldopa
Cold Agglutinin
IgM
seen in CLL, mono, mycoplasma pneuomnia
Microangiopathic anemia
schistocytes
weird causes of microangiopathic anemia
malignant htn
sle
Iron Def Labs
decreasd Iron
increased TIBC/transferrin
decreased ferritin
decreased transferrin saturation (serum iron/TIBC)
transferrin saturation
iron/TIBC
Chronic disease labs
decreased iron
decreased transferrin/TIBC
increased ferritin
Hemochromatosis labs
increased iron
decreased transferrin
increased ferritin
increased transferrin saturation
Pregnancy/OCP lab values
increased transferrin/TIBC
decreased transferrin saturation
transferrin
transport iron in blood
ferritin
primary iron storage protein
Hemophilia A
def of VIII increase PTT
Hemophilia B
def of IX increase PTT
Vit K def
decrease synthesis of 2,7,9,10, protein C and S
Hodgkin’s Lymphoma
associated with EBV
Reed-Sternberg Cells
B signs/symptoms
localized nodes
Non-Hodgkin’s Lymphoma
multiple, non contiguous nodes
mostly involving B cells
associations with HIV and immunnosuppresion
Reed-Sternberg Cells
CD 30+, CD 15+ B cells
plasma cells with clock face
Multiple Myeloma
ALL
<15 years
often mediastinal mass
increased lymphoblasts
Hair Cell Leukemia
B cell tumor in elderly
TRAP positive
Hairy Cell Leukemia treatment
cladribine
adenosine analog
AML
Auer rods
older onset
DIC common
t(9:22)
CML
philadelphia chromosome
bcr-abl
t(8:14)
Burkitt’s lymphoma
c-myc activation
t(11:14)
cyclin D1 activation
mantle cell lymphoma
T(14:18)
follicular lymphomas
bcl-2 activation
Polycytehmia vera
Jak2 mutation
increased, RBC, WBC, platelets
JAK 2 mutation
polycytehmia vera
deficient alpha-aminolevulinic acid
lead posioning
symptoms of lead poisoning
mental deterioation, sideroblastic anemia
anti-GpIIB/IIIa antibodies
ITP
increased megakarocytes
ITP
ADAMTS 13
vWF metalloprotease
TTP
ITP, TPP lab values
increased BT
normal PT, PTT
polycythemia symptoms
itching after shower (increased histamine)
ruddy skin
palpable spleen
conseuqence of HIT
deep vein and arterial thrombosis
Hereditary Angioedema
swelling of eyelids and lips
decrease C1 esterase inhibitor
Heparin
anti-coagulant
cofactor for activation of anti-thrombin
Warfarin
chronic anti-coag
interferes with synthesis and carboxylation of vit K dependent clotting factors
Heparin monitoring
PTT (intrinsic)
Warfarin monitoring
PT/INR (extrinsic)
Warfarin overdose treatment
IV vitamin K and fresh frozen plasma
ribavirin SE
hemolytic anemia
Hodgkin’s lymphoma treatment
Bleomycin
Pacitaxel use
ovarian and breast carcinomas
A blood Group
A antigen on RBC
anti-B antibody
B blood Group
B antigen
anti-A antibody
AB blood group
A, B antigens
no antibodies
universal recipient of RBC
universal donor of plasma
O blood group
Anti-A and Anti-B antibodies
universial donor of RBCs
universal recipient of plasma
HbH
deletion of three alpha genes
excess Beta globulin forms Beta-4 (HbH)
Plummer-Vinson syndrome
iron def anemia
esophageal webs
atrophci glossitis