Hematology Flashcards

(60 cards)

1
Q

MCC of leukopenia

A

Drug toxicity

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2
Q

MC Cancer in children

A

ALL

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3
Q

genetic abnormality in Acute ALL

A

t(12;21), t(9;22)

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4
Q

BM biopsy of AML criteria

A

> / 20% myeloblast

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5
Q

needlike-azurophilic granules in the cytoplasm

A

Auer rods

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6
Q

Genetic mutation t(15;17)
Auer rods
Faggot cells
assoc with DIC
80% curable with All trans retinoic acid

A

Acute promyelocytic anemia

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7
Q

MC leukemia of adults in Western world

A

CLL/SLL

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8
Q

CLL – progression to DLBCL

A

Ritcher phenomenon

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9
Q

BCR-ABL t(9;22)
Philadelphia chromosome
Splenomegaly
hyperceullar marrow/sea blue histiocytes
WBC >100,000
Low leukocyte alkaline phosphatase

A

CML

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10
Q

MC Classical HL

A

Nodular sclerosis

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11
Q

Classical HL worst prognosis and associated with PLHIV patients

A

Lymphocyte Depleted HL
90% assoc with EBV

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12
Q

Immunohisto chem of HL

A

CD15 CD30
NLPHL - + CD20

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13
Q

General lymphadenopathy and extranodal involvement (BM, spleen, liver, gut)
Leukemic presentation
t (11;14)
aggressive and incurable

A

Mantle cell Lymphoma

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14
Q

MC form of indolent NHL

A

Follicular Lymphoma

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15
Q

MC NHL

A

Diffuse large B cell lymphoma
aggressive, large cells, diffuse, atypia

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16
Q

one of the fastest growing tumor
assoc with latent EBV infection
high mitotic and numerous apoptotic cells
Starry sky pattern
good response to chemo

A

Burkitt Lymphoma

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17
Q

Splenomegaly
Pancytopenia
dry tap on BM aspiration
Monocytopenia
Cells: Hair like projections
BRAF V600E mutation
+ TRAP

A

Hairy cell leukemi

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18
Q

HM: large anaplastic cells with horseshoe-shaped nuclei
CD30
ALK mutation

A

Anaplastic Large cell lymphoma

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19
Q

T cells with Cerebriform nuclei

A

Sezary cells
Sezary syndrome = gen exfoliative erythroderma + leukemia of Sezary cells

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20
Q

CD4 T Cell tumor of the skin

A

Mycosis fungoides/Sezary syndrome

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21
Q

most important plasma cell neoplasm

A

Multiple myeloma

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22
Q

5 classical HL

A

Nodular sclerosis
Mixed cellularity
Lymphocyte rich
Lymphocyte depleted
Nodular lymphocyte predominant

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23
Q

Globular CYTOPLASMIC inclusion seen in MM

A

Russel bodies

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24
Q

Globular NUCLEAR inclusion seen in MM

A

Dutcher Bodies

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25
Clinical presentation of MM
CRAB hyperCalcemia Renal failure Anemia Bone lesion -- punched out (MC site VC)
26
PBS findings in MM
Rouleaux formation Plasma cell leukemia
27
Mutation in Myeloproliferative neoplasm
JAK2
28
PBS finding in Primary Myelofibrosis
Leukoerythroblastosis Tear drop cells/Dacrocytes
29
Type of necrosis: Bland Infarct
Coagulative necrosis
30
Type of necrosis: Septic infarct
Suppurative necrosis
31
All intrinsic types exhibit EXTRAVASCULAR Hemolysis, Except
PNH (intravascular)
32
XR , low NADPH Heinz bodies in asplenic px Bite cells/Degmacytes in functional spleen Protective against malaria
G6PD deficiency
33
mutation of 6th codon of the B-globulin gene (glutamate --> valine)
Sickle cell anemia
34
Findings in Sickle cell Anemia
Drepanocyte (sickle cells) target cells (Codocyte) Howell Jolly Bodies extramedullary hematopoises
35
Treatment for Sickle Cell Anemia
Hydroxyurea -- increases HbF
36
infants do not become symptomatic until
5-6 months of age --- HbF prevent sickling
37
symptoms appear in B- Thalassemia
6-9mos of age
38
symptoms appear in A- Thalassemia mutation:
at birth (low HbF synthesis) mutation deletion
39
1 gene affected in A-thalassemia
Silent carrier
40
2 gene affected in A-thalassemia
a- thalassemia trait minor
41
3 gene affected in A-thalassemia
HbH disease Severe, like B-thalassemia intermediate
42
4 gene affected in A-thalassemia
Hydrops fetalis
43
PIGA mutations in PNH
CD55, CD59(most important), C8 binding protein
44
fragmented RBC seen where
Schistocytes microangiopathic HA
45
MC nutritional disorder in the world
IDA
46
microcytic hypochromic pencil cells low serum Fe high transferrin low ferritin
IDA
47
Common cause of anemia in hospitalized px
Anemia of Chronic Inflammation
48
Px with chronic microbial infection low serum Fe Low transferrin increase ferritin
Anemia of Chronic Inflammation
49
Pancytopenia Hypocellular bone marrow Normocytic Normochromic
Aplastic Anemia
50
Preferential infection of erythroid precursor
Parvovirus
51
MCC of Myelophthisic anemia
Metastatic cancer
52
Features of TTP
Micronagiopathic HA Thrombocytopenia Renal Failure Fever Neurologic manifestation
53
Syndromes under HUS
Microangipathic HA Thrombcytopenia Renal failure
54
Pathogenesis of HUS
typical: E. coli O157:H7 (Shiga like) --> endothelium procoagulant Atypical: defect in excessive complement activation --> thrombosis
55
Pathogenesis of TTP
low ADAMTS13
56
MC inherited bleeding disorder
Von Willebrand disease AD, impaired PF
57
MC hereditary disease
Hemophilia X-linked, abnormality in Factor VIII (A), Factor IX (B)
58
bilateral adrenal hemorrhage secondary to fibrin thrombi
Waterhouse-Friederichsen syndrome
59
MC adverse transfusion reaction
Febrile Non-Hemolytic transfusion reaction
60
MC reaction encountered in platelet transfusion
Allergic Rhinitis