Haematology PassMed Flashcards

1
Q

name the 4 types of Hodgkins lymphoma

A

nodular sclerosis
mixed cellularity
lymphocyte predominant
lymphocyte depleted

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2
Q

which Hodgkins lymphoma is most common

A

nodular sclerosing

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3
Q

what does a reed Sternberg cell look like

A

a nuclei surrounded by a clear space

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4
Q

what disease is associated with smear cells

A

CLL

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5
Q

what are the CRAB features that myeloma typically presents with

A

Calcium elevated
Renal failure
Anaemia
Bone pain

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6
Q

when in myeloma is Alk phos usually only elevated

A

usually only in metastatic disease

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7
Q

how is vWF deficiency inherited

A

autosomal Dominant

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8
Q

how is a stage 3 Hodgkins lymphoma defined

A

involvement of LN regions on both sides of the diaphragm

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9
Q

which infection has strong links with lymphoma

A

EBV

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10
Q

what is a rouleaux formation and what is it characteristic of

A

a stacking of RBCs seen in a blood film

it suggests a myeloma

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11
Q

what is a ‘pepper pot skull’ characteristic of

A

primary hyperparathyroidism

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12
Q

what is a ‘rain drop’ skull characteristic of

A

myeloma

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13
Q

what are the 3 components of the diagnostic criteria for myeloma

A
  1. plasmacytoma
  2. 30% plasma cells in bone marrow sample
  3. elevated levels of M protein in the blood or urine
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14
Q

what is a plasmacytoma

A

a tumour of plasma cells that grows in the soft tissue, characteristic of a myeloma

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15
Q

how does factor V Leiden increase chance of VTE

A

activated factor V is inactivated much more slowly by activated protein C

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16
Q

what age is NHL most common

A

it has a bi modal age distribution

most common in 3rd and 7th decade

17
Q

if you suspect lytic bone metastases in a patient with renal failure and anaemia, what investigation do u do

A

serum protein electrophoresis

ie - urinary Bence Jones protein

18
Q

in sickle cell, what are thrombotic crises precipitated by

A

infection, dehydration, deoxygenation

19
Q

describe the signs of acute sickle chest syndrome

A

SO, chest pain, pul infiltrates, low Po2

20
Q

how is a non-haemolytic febrile reaction treated

A

temporary transfusion termination and an antipyretic (paracetamol)

21
Q

what transfusion reaction can DIC be a complication of

A

acute haemolytic transfusion reaction

22
Q

what Ig is usually responsible for acute haemolytic transfusion reaction

23
Q

what is the cause of non-haemolytic febrile reaction

A

white blood cell HLA antibodies

24
Q

how do you differentiate between allergic anaphylaxis transfusion reaction and acute haemolytic transfusion reaction

A

allergic - urticaria, hypotension, SOB, wheezing and stridor

acute haemolytic - fever, ab pain, chest pain, agitation and hypotension

25
what are the signs of transfusion related acute lung injury
development of hyperaemia/ARDS within 6hrs of transfusion has pul infiltrates on XR
26
what is the main difference between transfusion related acute lung injury and transfusion associated circulatory overload
TACO has hypertension, TRALI has hyPOtension
27
what deficiency causes a megaloblastic anaemia
B12 and Folate
28
if a patient is going to be treated for folate deficiency with folic acid, what is it important to replace 1st? why ?
treat the B12 deficiency 1st to avoid precipitating subacute combined degeneration of the cord
29
what mutation is seen in most polycythemia vera patients
JAK2 mutation
30
what cancer may myelodysplasia progress to
AML
31
what is tumour lysis syndrome and what can it result from
results from cell breakdown following chemotherapy this releases lots of intracellular components such as K, P04 and uric acid
32
which tumour can cause tumour lysis syndrome when it is treated using chemotherapy
burrkitt's lymphoma
33
in what disease is an osmotic fragility test diagnostic
hereditary spherocytosis
34
what is the one critical mediator of DIC
tissue factor
35
what role does TF play in DIC
TF binds to coagulation factors that then triggers the extrinsic pathway of coagulation, which goes on to trigger the intrinsic pathway
36
what does a typical blood pic look like in DIC
low platelets prolonged APTT and PT RAISED fibrin degradation products
37
what chromasome abnormality is seen in most CML patients
Philadelphia chromosome
38
what is the gene that results from a Philadelphia chromosome mutation and what does this gene code for
BCR-ABL a tyrosine kinase enzyme