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SAN FERNANDO, PAMPANGA

COLLEGE OF MEDICAL LABORATORY SCIENCE


MACROCYTIC ANEMIA

THE ORDER PERIPHERAL SMEAR TO EVALUATE FOR


HYPERSEGMENTED NEUTROPHILS THAT INDICATES
THE MEGALOBLASTIC ANEMIA

NON-MEGALOBLASTIC ANEMIA
MEGALOBLASTIC ANEMIA

OBTAIN RETICULOCYTE COUNT


TEST FOLATE AND VITAMIN B12 LEVELS

LOW HIGH

VITAMIN B12 LEVEL LOW FOLATE LEVEL LOW BOTH LEVELS LOW and NORMAL
EVALUATE FOR ALCOHOLISM, EVALUATE FOR
HYPOTHYROIDISM, OR HEMOLYSIS OR
Treat and retest, consider Treat and retest, HEPATIC DISEASE HEMORRHAGE
treating for pernicious provide dietary
anemia or ileal disease counseling
REFER TO PEDIATRIC HEMATOLOGIST
FOR CONSIDERATION OF BONE CAUSE UNKNOWN
NO IMPROVEMENT MARROW DISORDERS
DEFICIENCY DIAGNOSIS EVALUATION
Pernecious anaemia, Nutritional, Schilling’s test, Anti-IF and Anti Parietal
Vitamin B12
Malabsorption cell antibodies
Folate Nutritional, Malabsorption History and examination
Both Malabsorption History and examination
Inherited DNA synthesis defects,
None History
cytotoxic drugs

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NORMOCYTIC ANEMIAS
(MCV 80-100 um3)

Corrected reticulocyte count

<3% >3 %

 Blood loss <1 week INTRINSIC RBC DEFECT


EXTRINSIC RBC DEFECT
 Early-stage iron deficiency Membrane defects:
 Early-stage anemia  Hereditary spherocytosis  Blood loss >1 week
chronic disease  Hereditary elliptocytosis  Immune hemolytic anemias
 Aplastic anemia  Paroxysmal nocturnal  Micro/macroangiopathic
 Renal disease hemoglobinuria hemolytic anemia
 Malignancy Abnormal hemoglobins:  Malaria
 Sickle cell disease
Deficient enzymes:
 G6PD deficiency
 Pyruvate kinase deficiency

NORMOCYTIC ANEMIA:

TYPE OF NORMOCYTIC PERIPHERAL BLOOD BONE MARROW


ANEMIA
APLASTIC ANEMIA AA is defined by peripheral a hypoplastic bone marrow
blood pancytopenia with a that has fatty replacement

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hypocellular bone marrow in and that may have relatively
which normal hemopoiesis is increased nonhematopoietic
replaced to a greater or elements, such as mast cells
lesser extent by fat cells in
the absence of genetic,
malignant or predictable
myelosuppressive causes.
ACQUIRED APLASTIC ANEMIA AA is defined by peripheral Acquired aplastic anemia
blood pancytopenia with a (AA) is characterized by a
hypocellular bone marrow in hypoplastic, fatty bone
which normal hemopoiesis is marrow (BM) with profound
replaced to a greater or reductions in hematopoietic
lesser extent by fat cells in stem/progenitor cells
the absence of genetic, (HSCs/HPCs) that lead to
malignant or predictable defective mature blood cell
myelosuppressive causes. production and peripheral
pancytopenia
INHERITED APLASTIC ANEMIA Aplastic anemia occurs when
your bone marrow doesn't
make enough red and white
blood cells, and platelets.
Having fewer red blood cells
causes hemoglobin to drop.
FANCONI’S ANEMIA May look for dark spots on FA is a rare, inherited blood
the skin called café au lait disorder that prevents the
spots. The most common test bone marrow from producing
for Fanconi anemia is a blood enough new blood cells for
test called a chromosomal the body to function properly,
breakage test. or that causes the bone
marrow to make faulty blood
cells.
PURE RED CELL APLASIA Defined by a normocytic a bone marrow disorder
normochromic anemia with characterized by a reduction
severe reticulocytopenia and of red blood cells
marked reduction or absence (erythrocytes) produced by
of erythroid precursors from the bone marrow. Signs and
the bone marrow. Diamond- symptoms may include

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Blackfan anemia is a fatigue, lethargy, and/or
congenital form of PRCA abnormal paleness of the
skin (pallor) due to the
anemia the caused by the
disorder.
DIAMOND BLACKFAN-ANEMIA A bone marrow aspiration DBA the bone marrow cannot
and biopsy (removing a small make enough red blood cells
amount of the liquid portion of to meet the body's needs.
bone marrow through a DBA is characterized by a
needle) along with genetic shortage of red blood cells
testing can confirm the which usually becomes
diagnosis evident during the first year of
life when the patient develops
anemia
MYELOPTHISIC ANEMIA The peripheral blood smear Bone marrow fibrosis often
will show characteristic occurs as a secondary
leukoerythroblastic reactions process as well.
with the presence of Splenomegaly may develop.
immature myeloid and Characteristic changes in
nucleated erythrocytes, peripheral blood include
including abnormal anisocytosis, poikilocytosis,
erythrocytes such as and excessive numbers of
schistocytes, and dacrocytes red blood cell and white
(teardrop) and blood cell precursors.
anisopoikilocytosis cells

MACROCYTIC ANEMIA:

TYPE OF MACROCYTIC
PERIPHERAL BLOOD BONE MARROW MISCELLANEOUS
ANEMIA
MEGALOBLASTIC ANEMIA Megaloblasts are large bone marrow produces Form of anemia
nucleated red blood cell unusually large, structurally characterized by very large
precursors with no condensed abnormal, immature red blood red blood cells and a

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decrease in the number of
those cells. Anemias are
blood disorders that occur
when the body has fewer
chromatin. cells (megaloblasts) red blood cells than
normal. Red blood cells
carry oxygen throughout
the body using a protein
called hemoglobin.
the lack of folic acid in the
blood. Folic acid is a B
causes the body to produce the red blood cells are
vitamin that helps your
abnormally large red blood cells abnormally large. Such cells
body make red blood cells.
that cannot function properly. are called macrocytes. They
FOLATE DEFICIENCY If you don't have enough
Red blood cells carry oxygen are also called megaloblasts,
red blood cells, you have
around the body using a when they are seen in the
anemia. Red blood cells
substance called hemoglobin. bone marrow
carry oxygen to all parts of
your body.
Well recognized and reversible
Round macrocytes are Weakness and fatigue are
cause of bone marrow failure.
commonly seen in a variety of common symptoms of
Macrocytic anemias secondary
chronic illnesses, and round vitamin B12 deficiency.
to folate and/or vitamin B12
target-appearing macrocytes They occur because your
deficiency are characterized by
VITAMIN B12 DEFICIENCY are characteristic of liver body doesn't have enough
typical morphological
disease such as hepatitis, vitamin B12 to make red
abnormalities in the bone
obstructive jaundice, and acute blood cells, which transport
marrow, attributable to flaws in
and chronic alcoholism with liver oxygen throughout your
both the synthesis and repair
disease body.
of DNA
Disease conditions can also Malabsorption is a clinical
limit iron absorption; this can term that refers to the
happen as a result of insufficient impaired absorption of
bone marrow produces
stomach acid, lack of intrinsic nutrients. It encompasses
unusually large, structurally
IMPAIRED ABSORPTION factor (IF), celiac disease, defects that occur during
abnormal, immature red blood
inflammatory conditions such as the digestion and
cells (megaloblasts)
Crohn's disease, and in absorption of food nutrients
autoimmune diseases and by, and infections of, the
hormone imbalances. gastrointestinal tract

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COLLEGE OF MEDICAL LABORATORY SCIENCE

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