Week 3 Review Flashcards

1
Q

features of atypical lymphocytes on blood film?

A

larger
activated cytoplasm (irregular shape, not smooth and round, scallops around edges of surrounding red cells)
blueish cytoplasm due to proteins

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2
Q

activated lymphocytes can be seen in response to what?

A

mainly viruses

  • EBV
  • HIV
  • others including URTI - RSV, flu, parainfluenza etc
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3
Q

how does EBV affect lymphocytes?

A

infects epithelial cells in throat (sore throat)
infects lymph node tissue (enlarged tonsils and lymph nodes)
infects B cells causing proliferation (infected B cells proliferate which also allows proliferation of virus)
T cells recruited to fight infection (reactive T cells)

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4
Q

how is EBV diagnosed?

A

IgM antibodies against EBV

has to be IgM as IgG shows past infection

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5
Q

what shouldnt be given in EBV?

A

antibiotics

amoxycillin induced rash occurs (diagnostic)

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6
Q

what is lymphadenopathy?

A

enlarged nodes

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7
Q

types of lymphadenopathy?

A

regional

generalised

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8
Q

causes of regional lymphadenopathy?

A
bacterial abscess
metastatic cancer (first spreads to regional nodes)
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9
Q

causes of generalised lymphadenopathy?

A
viral infection (most common, can take a long time to resolve)
connective tissue disorders
rheumatoid arthritis
sarcoidosis (hilar lymphadenopathy)
lymphoid malignancy (lymphoma etc)
metastatic cancer
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10
Q

describe nodes in viral infection

A
tender
hard
smooth
no skin inflammation
no tethering
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11
Q

features of neutrophils which are responding to bacterial infection/inflammation?

A

lots more granules
big vacuoles
“toxic granulation and vacuolation)

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12
Q

leucocytosis?

A

high WCC

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13
Q

causes of neutrophilia?

A
bacterial infection
inflammation (e.g RA)
trauma
post surgery
corticosteroids (aparent neutrophilia)
myeloproliferative disease (CML, myelofibrosis etc)
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14
Q

causes of lymphocytosis?

A

viral infection (often also has mild neutropenia/thrombocytopenia)
pertussis
childhood response to infection
chronic lymphocytic leukaemia (smear cells)

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15
Q

when would you suspect hodgkins disease rather than non-hodgkins?

A
young patient (esp female)
disease only above the diaphragm
presence of B symptoms 
itch
alcohol induced pain
but really need a biopsy
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16
Q

commonest cause of hodgkins disease?

A

nodular sclerosing

nodules of tissue with malignant cells in them along with bands/scars of scar tissues in between (sclerosing)

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17
Q

characteristic cells of hodgkins?

A

reed sternberg cells

also usually have a reactive infiltrate of monocytes and lymphocytes which stimulate the sclerosis

18
Q

what are reed sternberg cells?

A

used to be B cells

bc of the mutation which has occurred causing the malignancy they have become abnormal with few normal surface proteins

19
Q

high grade NHL?

A

full of immature cells (blasts) which are large with prominent nucleoi
high mitotic rate

20
Q

low grade NHL histology?

A

full of mature lymphocytes

normal size cells grow more slowly and gradually accumulate

21
Q

what does leucoerythroblastic mean?

A

immature circulating RBC and WBC precursors

22
Q

what does leucoerythroblastic picture on blood film indicate?

A

wither

  • marrow infiltration (cancer, fibrosis - immature cells being pushed out as marrow is replaced with abnormal stuff)
  • marrow is under stress (sepsis, major bleeding, shock)
23
Q

how does stage of hodgkins disease relate of 5 year survival?

A
1 = 90%
2 = 80%
3 = 70%
4 = 50%
24
Q

how is hodgkins disease staged?

A

CT

PET scan

25
Q

cause of pancytopenia in chemo?

A

chemo kills rapidly growing cells so lymphoma cells are killed but so are the normal immature cells undergoing mitosis in bone marrow

26
Q

general immediate side effects of chemo?

A

bone marrow suppression
gut mucosal damage
hair loss

27
Q

bone marrow biopsy in aplastic marrow related to chemo?

A

mainly fat cells

28
Q

consequences of bone marrow failure (hypoplastic/aplastic marrow)

A

anaemia
neutropenia (infections)
bleeding

29
Q

what infections often occur in neutropenia and why?

A

gram -ves (mainly)

coliforms released from damaged gut (due to chemo) can enter the blood stream

30
Q

what later infections can occur after chemo if neutrophil count doesnt recover?

A

fungal
aspergilloma (aspergillus fungus)
therefore often given prophylactic antifungals

31
Q

commonest causes of increased destruction of cells causing a pancytopenia?

A

autoimmune destruction

sepsis

32
Q

causes of decreased production of blood cells causing a pancytopenia?

A
infiltration of marrow (malignancy etc)
B12 deficiency
aplastic anaemia
drugs (chemo)
viruses
radiation
33
Q

what else can cause pancytopenia?

A

sequestration of blood cells in spleen (hypersplenism - most commonly due to liver cirrhosis)

34
Q

approach to diagnosing pancytopenia?

A

history > exam > investigations (reticulocyte count, B12/folate, abdominal US etc) > bone marrow biopsy (check whether hypo/hypercellular)

35
Q

causes of hypocellular marrow?

A

drug induced aplasia (cytotoxic drugs etc)

36
Q

causes of hypercellular marrow?

A
infiltration
peripheral destruction (hypersplenism)
37
Q

what types of supportive therapy is used in haematological malignancy?

A

prompt treatment of infections with broad spectrum antibiotics
use of hickman line (indweling catheter in SVC)
red cell transfusions
platelet transfusions

38
Q

when should haematology sepsis protocol be started?

A

pyrexia and neutropenia <0.5 x 10/L

39
Q

when might splenectomy be used?

A

to treat immune thrombocytopenic purpura and autoimmune haemolytic anaemia

40
Q

what system is spleen a part of?

A

reticuloendothelial system

41
Q

what must be done after a splenectomy?

A

vaccinate for meningococcus, pneumococcus and haemophilus

prompt antibiotic use in case of fever