Anemias Flashcards
anemia
decrease below normal of one or more of the following:
o Number of red blood cells
o Hemoglobin
o Volume of packed red cells (hematocrit)
Loss of erythrocytes through bleeding must always be the FIRST FOCUS in any patient with anemi
HEMORRHAGE
a significant source of blood loss in women
Menstruation
shortened erythrocyte survival time NOT explained by bleeding
hemolysis
average survival time of RBCs after leaving bone marrow
120 days
decreased production of erythrocytes caused by
1) Nutritional deficiencies
2) Kidney disease
morphologic classifications of anemias based on
MCV, MCHC
MCV & MCHC in Normocytic , normochromic anemia
Both normal
described as a rare but potentially deadly bone marrow failure syndrome
APLASTIC ANEMIA
-most common of the inherited aplastic anemias
Fanconi Anemia (FA)
aplastic anemia, cancer susceptibility, and physical abnormalities
Fanconi Anemia (FA)
Fanconi Anemia vs Fanconi syndrome
FA - BM disorder
FS - PCT defect
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA aka
Marchiafava-Micheli Syndrome
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA caused by deficiency of
DAF & MIRL
TESTS for PNH
1) Ham’s acidified serum test
2) Sugar Water Test (sucrose hemolysis test)
3) Flow cytometry -
confirmatory for PNH
Flow cytometry
mcv & mchc both low
Microcytic, Hypochromic anemia
Microcytic anemia results from
iron level insufficient for maintaining normal eryhthropoiesis and
is characterized by abnormal results of iron studies
associated conditions in Microcytic, hypochromic anemia
“TAILS”
Thalassemia Anemia of Chronic inflammation Iron Deficiency Anemia Lead poisoning Sideroblastic anemia
most common anemia among hospitalized patients
Anemia of chronic inflammation (ACI)
body stores have abundant iron; red cells are deficient in iron
Anemia of chronic inflammation (ACI)
Central feature of ACI:
sideropenia (↓ serum iron) despite abundant iron stores
Acute phase reactants (APRs) that contribute to ACI
1) Hepcidin
2) Lactoferrin
3) Ferritin
hallmark of the sideroblastic anemias
Ring sideroblasts
The “rings” in ring sideroblasts
mitochondria loaded with iron
Dimorphic peripheral blood picture
(normochromic and hypochromic RBC
Sideroblastic anemias
Iron is trapped in the mitochondria (cannot be fully utilized in Hb synthesis
anucleate RBC w/ iron granules
SIDEROCYTE
nucleated RBC precursor with cytoplasmic iron granules
SIDEROBLAST
– the most common anemia
Iron deficiency anemia (IDA)
clinical features of IDA:
Koilonychia (spooning of the fingernails)
glossitis
angular cheilosis
pica
TIBC = low
Serum ferritin = High
ACI
TIBC = High
Serum ferritin =low
IDA
(MCV= HIGH, MCHC=NORMAL
MACROCYTIC, NORMOCHROMIC ANEMIAS
MACROCYTIC, NORMOCHROMIC ANEMIAS
1) MEGALOBLASTIC ANEMIA NONMEGALOBLASTIC ANEMIA 2) NONMEGALOBLASTIC ANEMIA
NONMEGALOBLASTIC
ANEMIA
“LAB”
1) Liver disease
2) Alcoholism (chronic)
3) Bone marrow failure
- characterized by the presence of
antibodies against parietal cells and
antibodies against IF
*PA (Pernicious Anemia)
competition with vit B12
D. latum
H. pylori
Hypersegmented nuetrophils Present in this type of anemia
Megaloblastic anemia
macocyte shape in Megaloblastic anemia
oval
considered as root cause of megaloblastic anemia
Impaired DNA synthesis
: thymidine triphosphate (TTP)
important structure of which DNA synthesis is dependent on
vit. B12 aka
Cobalamin
- synthetic form of vitamin B12 (found only in supplements)
Cyanocobalamin
naturally occurring form that may be obtained from either food sources or supplements
Methylcobalamin
Blood pictures seen in folate deficiency and vitamin B12 deficiency
indistinguishable
Other possible findings in megaloblastic anemia
teardrop cells, nucleated RBCs, Howell-Jolly bodies, basophilic stippling, and Cabot rings
haptocorrins
vit. B12 s bound to transcobalamin I and III
metabolically active
form of Vitamin B12.
holotranscobalamin (holoTC)