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Ibrahim Qaqish, MD, FACP, Raj Ravula, MD, St. Josephs Hospital & Medical Center
Anemia
RBC Mass/Hgb
R/0 Dilutional Anemia
example:- Pregnancy, CHF
volume overload
80-95 FL
<80 FL
Microcytic
>95 FL
Normocytic
RI 2
Macrocytic
RI 2
Normal, High
>110FL
Low
Hemoglobin Electrophoresis
7
B Deficiency
12
Blood Smear
Macroovalocytes
Hypersegmented
neutrophils
homocysteine
Normal, High
LDH, Peripheral Smear
Indirect bilirubin
Low
Thalassemia Minor
Serum Fe
TIBC
5
Anemia of chronic disease
Sideroblastic Anemia
Pappenheimer bodies
Basophilic Stippling
BM Biopsy
Ring Sideroblasts
Auto Immune
SLE, Thymoma, congenital
Fanconis
Lead Poisoning
Congenital
Fanconi
Copper Deficiency
Hypothermia
Isoniazid, Chloramphenicol
Myelofibrosis
Myelophthesis
Fat, Malignant cells
Gauchers disease, Leukemia
BM biopsy
Pure Red
cell Aplasia
Aplastic anemia
50% Indiopathic
Infections-HIV, EBV, CMV,
HCV
Radiations, Chemicals
Normal
Peripheral Smear
Normal
Low
Pancytopenia
BM Biopsy
Peripheral Smear
Hemolysis4
Retic
Normal LDH
Parvo Virus
PCR
95-110FL
Schilling Test
Renal Failure
GFR
Erythropoietin
Blood smear-Burr cells
Liver Disease
Abnormal LFT
Hypothyroidism
3
Anemia of
Chronic disease
MMA
High
Normal, Low
RBC, Folate
7
Low
Folate Deficiency
homocysteine
Congenital
7) B12, Folate deficiency - LDH, indirect bilirubin may be elevated due to ineffective erythropoiesis
Peripheral
Smear
Elliptocytosis
Eltiptocytes
GEPD
PNH
Paroxysmal
Nocturnal
Hemoglobinuria
Hereditary
Spherocytosis
Osmotic fragility Test
Spherocytes
Ham Test
Sugar water Test
Flow cytometry
Assay CD 55
Pyruvate
Kinase
Deficiency
Reticulocytosis
-Secondary to
bleeding,
hemolysis
Non-Immunological
Hemoglobinopathies
GEPD RBC
enzyme assay
Congenital
PK RBC
enzyme assay
RI 2
Extravascular
Hgb electrophoresis
Sickle Cell
SS
Thalassemia
-Infant +
craniofacial
anatomy or
absent radius
or urogenital
anatomy
Myelodysplastic
Diamond-black fan
syndrome
syndrome
-Usually Pancytopenia
-Peripheral Smear
Pseudo-Pelger-Huet anamoly
-BM (Blast + ring sideroblasts)
Immunological
Intravascular
Monoclonal - lymphoproliferative
Polyclonal
Hypersplenism
Microangiopathic
Hemolytic Anemia
8 TTP, DIC, HUS(no neurologic deficit)
HELLP Syndrome
Schistocytes
Peripheral Smear- helmet cells
fragmented RBC
Spherocytes
- mycoplasma pneumoniae
- mononucleosis
- Paroxysmal cold
hemoglobinuria
- Alloimmune - blood transfusion
- Platelets -ITP Evans Syndrome
Sickle / thal
Anemia
Usually B
thalassemia
trait
minor
Hb H
Hb barts
B Thalassemia
Major
Minor
Vasculitis
Infections
Invasive
- Malaria
- Babesiosis
Toxin
- Clostridium perfringens
- Borreliosis
Intravascular
Extravascular
Schistocytes
Spherocytes
/ absent
Mild decrease
Urine hemoglobin
++
Negative
Urine hemosiderin
++
Negative
Usually ++
++++
Peripheral Smear
Haptoglobin
Guyatt GM et al. Laboratory diagnosis of iron deficiency anemia. J Gen Int Med 1992;7:145-53
Griner PF.Microcytosis. In: Diagnosis Strategies for Common Medical Problems. ACP ; 1999:575-584
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Peripheral
Smear
BM Biopsy
Acquired
Stomatocytosis
Hypophosphatemia
8) TTP Pentad - Fever, thrombocytopenia, MAHA, Renal failure and nuerological deficit.
Same in HUS without neuroligical deficit
9) Ferritin level <10 in females, <20 in males confirms iron deficiency anemia while level>200 excludes it.
Levels between 20-200 bone marrow aspirate and if iron levels are low, confirms iron deficiency.
Ferritin is usually high in anemia of chronic disease.
Normal, Low
Fe, TIBC
Ferritin
Extrinsic
Methemoglobinemia
2
3
Fe
Fe
TSH
Enzymatic
Acquired
Normal
High
Hypothyroidism
3
NOTES:
LFT
Abnormal
Anemia of Liver Disease
Alcholism
Intrinsic
Membranopathy
Normal, High
LDH