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61 Cards in this Set

  • Front
  • Back
RBC count in males (normal)
4.3-5.9 x 10^6/mm^3
(increased/normal in thalassemia)
(decreased in iron deficiency)
(both microcytic - good way to distinguish)
RBC count in females (normal)
3.5-5.0 x 10^6/mm^3
HGB in males (normal)
13.6-17.2 gm/dl
HGB in females (normal)
12.0-15.0 gm/dl
HCT in males (normal)
39-49%
(RBC number X MCV)
HCT in females (normal)
33-43%
(RBC number X MCV)
MCV (normal)
76-100 fL
<70 microcytosis
>100 macrocytosis
MCH (normal)
27-33 pg
(HGB/RBC number)
MCHC (normal)
33-37 gm/dl
(Hemoglobin Concentration/HCT X 100)
(elevated in spherocytosis)
(decreased in microcytic hypochromic anemias)
RDW (normal)
11.5-14.5
t(9;22)
CML
(in anything else - poor prognosis)
t(8;14)
Burkitt's Lymphoma
t(14;18)
Follicular Lymphoma
t(15;17)
AML - M3 (good prog)
t(1;14)
T-cell Lymphoblastic Lymphoma
t(11;22)
Ewing's Sarcoma
t(11;14)
Mantle Cell Lymphoma
t(11;18)
MALT Lymphoma
t(12;21)
ALL (good prognosis)
t(4;11)
ALL (poor prognosis)
PSA
Prostate Cancer
CEA
Colorectal
Pancreatic
CA 19-9
Pancreatic
AFP
Hepatic
Yolk Sac
BHCG
Choriocarcinoma
Molar Pregnancy (triploid fetus)
CA 125
Ovarian Cancer
S-100
Melanoma
Astrocytoma
Thyroglobulin
Thyroid Cancer
Calcitonin
Medullary Carcinoma of Thyroid
Catecholamines (blood)
Metanephrines (urine)
Pheochromocytoma
Neuroblastoma
TRAP stain
Hairy Cell Leukemia (acute)
(tartrate resistant acid phosphatase)
Alkaline Phosphatase
Mets to bone
Paget's disease of bone
Test for heriditary spherocytosis . . .
osmotic fragility
Difference between TTP and HUS . . .
HUS is similar but . . .
- no CNS problems
- increased renal problems
Drepanocytes
another term for sickle cells
(b/c "sickle cell" is too obvious)
anisocytosis
size variation
poikliocytosis
shape variation
Leukemoid Reaction vs CML
LAP >100 - Leukemoid rxn
LAP <10 - CML
What type of leukemia/lymphoma is:
PAS +
MPO -
ALL
What type of leukemia/lymphoma has auer rods?
AML (diagnostic)
- eosinophilic cytoplasmic deposit
- made of azurophilic granules
What are the two viruses associated with leuk/lymph?
EBV - Burkitts Lymphoma
EBV - PTLD (post transplant lymphoproliferative disorder)
HTLV-1 - Tcell leuk/lymph
(Also remember that H. Pylori is ac/w MALT Lymphoma)
CD 5+ 23+
CLL/SLL
CD 5 - Tcell marker
CD 23 - Bcell marker
(shows neoplastic nature of cells)
ALL vs CLL
acute versus indolent
acute process will respond to chemo
acute has blastic, fine, delicate chromatin while chronic is condensed
3 phases of CML
chronic <5%
accelerated 10-19%
blast >20%
4 main types of myeloproliferative disorders
Chronic myelogenous leukemia (myeloid)
Chronic idiopathic myelofibrosis (megakaryocytes)
Essential thrombocytopenia (megakaryocytes)
Polycythemia vera (RBCs)
AML - M0
Minimally differentiated
(blasts lack myeloid features)
AML - M1
Myeloid w/o maturation (20%)
- MPO+
AML - M2
Myeloid w/ maturation (30-40%)
- t(8;21) - good prognosis
AML - M3
Promyelocytic
- complicated by DIC
- t(15;17) - good prog
AML - M4
Myelomonocytic
- NSE+
- inv 16 - good prog
AML - M5
Monocytic
- t w/ 11q23 - bad prog
AML - M6
Erythroid
AML - M7
Megakaryocytic
- ac/w Down synd.
Leuk/lymph special stains
PAS
MPO
SBB
NSE
PAS - ALL

The rest are + in AMLs
MPO - myeloblasts
SSB - myelo + monoblasts
NSE - monoblasts
AML + Down Synd
AML - M7 (megakaryocytic)
AML complicated by DIC
AML - M3 (promyelocytic)
ALL vs AML
ALL - Childeren
AML - Adults

Also in ALL
MPO-
PAS+
CD 10+ (aka CALLA)
abrupt onset
bone pain
CNS involvement
t(8;21)
AML - M2 (good prog)
inv 16
AML - M4 (good prog)
t w/ 11q23
AML - M5 (bad prog)
ALL - also bad prog
(multilineage leukemia gene)
Doehle bodies
dilated patches of ER
(what diseases)