Pathophysiology Flashcards

1
Q

t(8:14) translocation

A

burkitts lymphoma
(pronounced burk8’s)

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2
Q

t(11:14) translocation

A

mantel cell lymphoma
also associated with CD 5

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3
Q

t(11:18) translocation

A

marginal zone lymphome

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4
Q

t(14:18) translocation

A

follicular lymphoma (BCL-2 activation)

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5
Q

t(15:17) translocation

A

APL

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6
Q

t(9:22) translocation

A

philadelphia chromosome
CML

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7
Q

markers associated with ALL

A

CD 10 and TdT

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8
Q

markers assoicated with CLL

A

CD 5, CD 20, CD 23

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9
Q

haem malignancy associated with TRAP stain and what is it?

A

Hairy cell leukaemia
TRAP
Tartrate resistant acid phosphatase
(TRAPed in a hairy situation)

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10
Q

stary sky appearnace on microscopy

A

burkitts lymphoma

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11
Q

features of reed-sternberg cells and what condition they are found in

A

hodgkins lymphoma
- CD 15 and CD 30 positive
- owl eyes (bilobed nucleus with 2 halves as mirror images)

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12
Q

most common type of hodgkins lymphoma

A

nodular scleroing

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13
Q

most common type of non-hodgkins lymphoma

A

diffuse large B cell

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14
Q

inherited thrombophillia with associated miscarriages

A

factor V leiden

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15
Q

causes of DIC

A

heat stroke, sepsis, obstetric complications, acute pancreatitis, malignancy, nephrotic syndrome, transfusions

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16
Q

basophillic nuclear remnants in RBC

A

howell jolley bodies (splenectomy or non-functioning spleen)

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17
Q

giant B cells with bilobed nucleus with prominent inclusion

A

(owls eye)
reed sternberg cells (hodgkins lymphoma)

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18
Q

hair on end appearance (crew cut) on x-ray

A

B thalassaemia or sickle cell anaemia
(due to marrow expansion)

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19
Q

sheets of medium sized lymphoid cells with scattered pale, tangible body-laden macrophages

A

‘starry sky appearance’
Burkitts lymphoma

20
Q

stacks of RBC

A

rouleux formation
found in multiple myeloma

21
Q

smudged WCC’s

22
Q

tennis racket shaped cytoplasmic organelles

A

langerhan cell histocytosis

23
Q

myeloperoxidase positive cytoplasmic inclusions with increasing circulating myeloblasts

A

Aeur rods (APL)

24
Q

anti-GpIIb/IIIa antibodies

A

immune thrombocytopenia

25
hypersegmented neutrophils
megaloblastic anaemia
26
basophillic stippling of RBC's
sideroblastic anaemia or thalassaemia
27
lab value of sideroblastic anaemia
high serum iron low ferritin (iron overload)
28
medication used to increase neutrophil count in patients who are neutropenic
filgrastim (granulocyte-colony stimulating factor)
29
what immunoglobulin is asociated with warm autoimmune haemolytic anaemia
IgG
30
what immunoglobulin is associated with cold autoimmune haemolytic anaemia
IgM
31
what factors are inhibited by antithrombin III
Vitamin K independant protease Vitamins II, IX, X
32
pathophysiology of thrombotic thrombocytopenic purpura
Microangiopathic haemolytic anaemia due to Ab against ADAMTS13 which is responsible for cleaving vWF Blood shows fragmented erythrocytes
33
drug that is used as prophylaxis for sickle cell patients
hydroxyurea increase HgF
34
Histology of kapsosai sarcoma
Spindle shaped cells with lymohocytic infiltrate
35
Presentation of acute haemolytic transfusion reaction
Fever Hypotension Abdominal pain
36
Fragmented erythrocytes
Microangiopathic haemolytic anaemia I.e. found in TTP
37
what tumour is associated with anti-NMDA Ab?
ovarian teratoma
38
tear drop poikoilocytes on blood film
thalassaemia megaloblastic anaemia myelofibrosis
39
pathophysiology of immune thrombocytopenic purpura (ITP)
antibodies directed against IIB/IIIC glycoprotein
40
RBC with an outer ring of haemoglobin surrounding a central condensation of haemoglobin
target cells - sickle cell
41
features of hydrops fetalis
fluid within 2 or more compartments in newborn baby causes i.e. alpha thalassaemia, Rh incompatability
41
hamaturia that resolves throughout the day
paroxysmal nocturnal haematuria
42
pathophysiology of paroxysmal nocturnal hamaturia
due to genetic defect of PIG-A gene resulting in impaired synthesis of GPI anchors = decreased extracellular complement inhibitors and haemolysis
43
mediastinal mass with light blue scanty non-granular cytoplasm
acute T cell lymphoblastic lymphoma
44
features of paroxysmal nocturnal haematuria
red urine in the morning that improves throughout the day pancytopenia venous thrombosis associated with acute leukaemias CD55/59 negative
45
pathophysiology of paroxysmal nocturnal haematuria
due to PIG-A mutation resulting in impaired synthesis of GPI anchoring proteins results in impaired inhibition of complement = hamolysis
46