Hematology Flashcards

1
Q

DIC in sepsis

A

Deranged coagulation

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2
Q

Cryoprecipitate constitution

A

factor 8 + fibrinogen + vWF + factor 13

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3
Q

Hemoarthroses, hematomas, prolonged bleeding; prolonged APTT

A

Hemophilia Factor 8 and 9

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4
Q

Factor 5 leidin

A

Activated protein C resistance

Inherited thrombophilia commonest

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5
Q

Tear drop poikilocytes

A

Myelofibrosis

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6
Q

Pencil piokilocytes

A

iron deficiency anemia

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7
Q

Howell-Jolly Bodies and Siderocytes

A

hyposplenism

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8
Q

Schistocytes

A

Hemolysis Such as Hereditary spherocytosis

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9
Q

Spherocytes

A

Hereditary spherocytosis or AIHA

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10
Q

CML treatment

A

Imatinib- TK inhibitor

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11
Q

Ritcher’s transformation

A

B symptoms - fever, weight loss, nigh sweats; CLL to large cell lymphoma; diagnose by biopsy of lymph node

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12
Q

DIC on coagulation test

A

Low platelet
Low fibrinogen
Increased PT and APTT
Increased FDPs

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13
Q

VTE risk

A

Factor 5 Leiden or Protein C resistance

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14
Q

Bleeding disorder that is inherited autosomal

A

VWF

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15
Q

Anti Tb medication, alcohol, myelodysplasia, lead and microcytosis are related to

A

Sideroblastic anemia

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16
Q

Basophilic stippling of cells - RBC

A

Sideroblastic Anemia

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17
Q

Most common type of leukaemia in adults

A

Chronic Lymphocytic Leukemia

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18
Q

Blood film of CLL

A

Smear cells aka Smudge cells

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19
Q

Petichae, purpura, epistaxis, in old females

20
Q

1st line management of ITP

A

Prednisolone

21
Q

Band cells

22
Q

BLAST CELLS

23
Q

Burkitt’s Lymphoma mutation

A

C-MYC gene translocation

24
Q

Clotting in Hemophilia - PT, APTT and Bleeding time

A

APTT increased
PT normal
BT normal

25
Coagulation test in VWD
APTT raised PT normal Bleeding time raised
26
Vitamin K deficiency coagulation
APTT increased PT increased Bleeding time normal
27
CLL to High grade non-Hodgkin lymphoma is called
Ritcher’s transformation
28
Tumour lysis syndrome
Lymphoma + Chemo + uremia, Hyperkalemia, hyperphosphatemia and hypocalcemia and increased creatinine/ Arrhythmia or seizure
29
Hypercalcemia; Pancytopenia and AKI, Proteinuria
Multiple myeloma
30
Myelodysplasia transforms into?
Acute myeloid Leukemia
31
Smudge cells or Smear cells
CLL
32
Pseudo-pelger Huet cells
CML
33
Back pain, >60, leukopenia and Hypercalcemia. choice of investigation
Protein electrophoresis and Bence-Jones protein testing
34
A painful maculopapular rash in a allogenic host
Graft vs Host disease
35
Isolated Low platelets
Commonly ITP
36
Anemia, Fever, purpura and cerebral dysfunction; a hematological disorder, low platelets, microangiopathic anemia, AKI
TTP
37
IgA deficiency increases the risk of blood transfusion reaction
Anaphylactic
38
EMA binding test is used for
Hereditary spherocytosis
39
Basophilic stippling and Cabot rings
Lead poisoning
40
Rouleaux formation
Myeloma
41
Lymphoma, Raynauld’s, worse on cold symptoms and new macrocytic anemia
AIHA
42
Ovarian cancer spreads
Locally
43
Myeloma - Calcium, Phosphate and ALP
High calcium Normal or high phosphate NOrmal ALP
44
Haemarthrosis is a sign of what hemotological disease
Hemophilia A
45
CLL is associated with what type of haemolytic anemia
Warm autoimmune anemia
46
COLD AIHA
Lymphoma, EBV, mycoplasma