HAEMATOLOGY Flashcards

1
Q

hypersegemented neutrophils

A

macrocytic anaemia - vitB12 or folate deficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

management of vitB12 def anaemia

A

1g IM hydroxycobalamin 3 times a week for 2 weeks
then every 3 months

if dietary can give oral oxocobalamin daily

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

management for folate def anaemia

A

oral folic acid daily for 4 months

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

anaemia symptoms
neuro symptoms
lemon tinge/mild jaundice

typically middle-old age female

A

pernicious anaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q
pancytopenia 
normocytic normochromic anaemia 
thrombocytopenia 
leukopenia
(anaemia symptoms, infections and bleeding)
A

aplastic anaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

definitive investigation for aplastic anaemia

A

biopsy - empty marrow or dry tap

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

management of aplastic anemia

A

remove any toxinx/meds/cause
if under 50 = stem cell transplant
if over 50 = immunosuppression with cyclosporine and glucocorticoids
severe cases = blood transfusion and GCS factor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

anaemia - pallor/ fatigue/ weakness
jaundice
splenomegaly

A

haemolytic anaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

investigation for haemolytic anaemia

A

coombs test - positive

normocytic anaemia on bloods

schistocytes and reticulocytes on blood film

IgM = cold HA
IgG = warm HA
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

management of haemolytic anaemia

A

first line = steroids (+/- rituximab)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

neonatal jaundice
splenomegaly
gallstones are common
anaemia

A

G6PD deficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Investigations of G6PD def anaemia

A

diagnostic = G6PD enzyme assay

also heinz bodies and bite/blister cells on blood film

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

management of G6PD def anaemia

A

avoid triggers

crisis = rehydrate and blood transfusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q
25yrs 
anaemia 
neutropenia
thrombocytopenia 
splenomegaly 
bone pain
A

AML

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

management for AML

A

chemotherapy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q
philadelphia chromosome
60-70yrs 
marked splenomegaly = abdo pain 
B symptoms 
and WBC at different stages of maturation
A

CML

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

management of CML

A

imatinib

(hydroxyurea, a-interferon and allogenic BM transplant)§

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q
male child
anaemia 
thrombocytopenia = brusing, bleeding or petechiae
bone pain 
hepatosplenomegaly
A

ALL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

management of ALL

A

chemotherapy +/- immunotherapy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

adult with marked lymphadenopathy, B symptoms, bleeding and infections, anaemia

21
Q

investigations for CLL

A

Immunophenotyping

smudge/smear cells on blood film

22
Q

management of CLL

A

watchful waiting if caught early

immunochemotherapy

23
Q

usually after injection/infection
can be in older females
bleeding
petechiae/purpura

24
Q

management of ITP

A

prednisolone and IVIG

sometimes splenectomy

25
adult female fever flutuating neuro signs renal failure
TTP
26
Investigations for TTP
ADAMTS13 IgG
27
management of TTP
plasma exchange corticosteroids rituximab
28
hypercalcemia, renal stones, anaemia, lytic lesions (on MRI)/ bence jones proteins (urine electrophoresis)
Multiple myeloma
29
management of multiple myeloma
Option 1 autologous SCT + bortezomib + dexamethasone Option 2 no SCT + thalomide + alkylating agent + dexamethasone monitor every 3 months - urine electrophoresis + blood tests acute relapses = bortezomib
30
associated with EBV or c-myc translocation either presents with jaw swelling/pain OR abdo pain, distension or ascites
burkitt's lymphoma
31
investigations for burkitt's lymphoma
starry sky appearance - apoptotic cells in macrophages
32
management of burkitt's lymphoma
chemotherapy
33
``` painless lymphadenopathy B symptoms alcohol consumption pain pruritus normocytic anaemia ```
hodgkin's lymphoma
34
reed sternberg/owl shaped/multinucleate
hodgkin's lymphoma
35
management of hodgkin's lymphoma
immunochemotherapy
36
diagnostic Ix for hodgkin's lymphoma
biopsy | reed sternbery cells
37
``` prolonged bleeding time lowered factor 8 epistaxis menorrhagia prolonged PT/APTT ```
von willebrand's disease
38
management of VWD
mild bleeding = tranexamic acid desmopressin factor 8
39
hemophilia A
factor 8 deficiency
40
hemophilia B
factor 9 deficiency
41
haemophilia C
factor 11 deficiency
42
haemarthrosis haematomas prolonged bleeding after surgery or trauma
haemophilia
43
management of haemophilia
IV infusion of desmopressin | and blood transfusion/correct coagulation factor deficiency
44
failure to thrive in first year of life hepatoplenomegaly - swollen abdomen microcytic anaemia jaundice
thalassemia
45
target cells on blood film | high iron/ferritin/TIBC
thalassemia
46
management of thalassemia
repeated transfusion | SC infusion of deferoxamine
47
management of thrombocytopenia
stop anticoagulation with heparin | only transfuse if pt is haemorrhaging
48
``` hyperviscosity pruritus, typically after a hot bath splenomegaly haemorrhage (secondary to abnormal platelet function) plethoric appearance hypertension in a third of patients associated with JAK mutation ```
polycythemia vera
49
management of polycythemia vera
venesection first line aspirin chemotherapy - hydroxyurea