Professional Documents
Culture Documents
Michael
Fu
• RED
BLOOD
CELL
DISORDERS
o Anemia
Microcytic
• Iron
deficiency
• Anemia
of
chronic
disease
• Thalassemia
• Sideroblastic
anemia
Macrocytic
• Folate
deficiency
• B12
deficiency
o Pernicious
anemia
Normocytic,
Reticulocyte
<
3%
• Acute
blood
loss
• Aplastic
anemia
• Early
iron
deficiency
• Early
anemia
of
chronic
disease
• Chronic
renal
failure
• Malignancy
Normocytic,
Reticulocyte
>
3%
• Non‐immune
hemolytic
anemia
o Hereditary
spherocytosis
o Hereditary
elliptocytosis
o Paroxysmal
nocturnal
hemoglobinuria
o Sickle
cell
o G6PD
deficiency
o Pyruvate
kinase
deficiency
o Acute
blood
loss
o Micro‐
and
macroangiopathic
hemolytic
anemia
o Malaria
• Autoimmune
hemolytic
anemia
o WAIHA
o CAIHA
• MYELOID
LEUKEMIA
o Chronic
myeloproliferative
disorders
CML
Polycythemia
vera
Myelofibrosis
and
myeloid
metaplasia
Essential
thrombocythemia
o Myelodysplastic
syndromes
Refractory
anemia
Refractory
anemia
with
ringed
sideroblasts
Refractory
anemia
with
excess
blasts
in
transformation
Chronic
myelomonocytic
leukemia
o AML
• LYMPHOID
LEUKEMIA
o ALL
o CLL
o Adult
T‐cell
leukemia
o Hairy
cell
leukemia
• LYMPHOMA
o Hodgkin’s
lymphoma
Nodular
sclerosing
Lymphocyte
dominant
Mixed
cellularity
Lymphocyte
depletion
o Non‐Hodgkin’s
lymphoma
B‐cell
lymphoma
• Burkitt’s
lymphoma
• Diffuse
large
B‐cell
lymphoma
• Extranodal
marginal
zone
lymphoma
• Follicular
lymphoma
• Small
lymphocytic
lymphoma
T‐cell
lymphoma
• Precursor
T‐cell
lymphoblastic
lymphoma
• Precursor
T‐cell
lymphoblastic
leukemia
• Mycosis
fungoides/Sezary
syndrome
o Langerhans
cell
histiocytoses
Letterer‐Siwe
disease
Hand‐Schuller‐Christian
disease
Eosinophilic
granuloma
o Mast
cell
disorders
Urticaria
pigmentosum
o Plasma
cell
dyscrasia
Multiple
myeloma
Monoclonal
gammopathy
of
undetermined
significance
Solitary
skeletal
plasmacytoma
Extramedullary
plasmacytoma
Lymphoplasmacytic
lymphoma
(Waldenstrom’s
macroglobulinemia)
Heavy‐chain
diseases
• HEMOSTASIS
DISORDERS
o Thrombocytopenia
Acute
idiopathic
thrombocytopenic
purpura
(ITP)
Chronic
idiopathic
thrombocytopenic
purpura
(ITP)
Neonatal
alloimmune
thrombocytopenia
Post‐transfusion
purpura
Heparin‐induced
thrombocytopenia
Thrombotic
thrombocytopenic
purpura
(TTP)
Hemolytic
uremic
syndrome
(HUS)
o Thrombocytosis
Primary
• Essential
thrombocythemia,
polycythemia
vera
Secondary
• Chronic
iron
deficiency,
infection,
malignancy,
splenectomy
o Coagulation
disorders
Hemophilia
A
Hemophilia
B
Classic
von
Willebrand
disease
Circulating
anticoagulants
Vitamin
K
deficiency
Hemostasis
disorders
in
liver
disease
Disseminated
intravascular
coagulation
(DIC)
o Fibrinolytic
disorders
Open
heart
surgery
Prostatectomy
Diffuse
liver
disease
o Thrombosis
syndromes
Acquired
thrombosis
syndromes
• Antiphospholipid
syndrome
• Malignancy
• Folate
or
B12
deficiency
• Oral
contraceptive
pill
Hereditary
thrombosis
syndromes
• Factor
V
Leiden
• Antithrombin
III
deficiency
• Protein
C
and
S
deficiency