Ha - Leukaemia Cases & Quiz Flashcards
how is a haematalogical diagnosis made
clinical sx
blood film
immunophenotyping
imaging
5 year old indian boy with lymphadenopathy & mediastinal mass on CXR.
High WCC, low Hb, low platelets. Dx?
ALL
5 year old indian boy with lymphadenopathy & mediastinal mass on CXR.
High WCC, low Hb, low platelets. what is the mediastinal mass?
thymus enlargement due to ALL
how is a diagnosis of ALL confirmed?
Immunophenotyping
is a high WCC in ALL good or bad?
BAD indicator for prognosis
48 year old with bleeding gums, haematuria and bruises. No hepatospelenomegaly. Low Hb and platelets. Dx?
acute promyelotic leukaemia –> DIC
48 year old with bleeding gums, haematuria and bruises. No hepatospelenomegaly. Most likely Ix to give Dx?
blood count, film and coagulation screen
Is APTT and PT long or short in DIC?
APTT is short
PT is normal
how do you identify myeloid and lymphoid cells?
granules suggest myeloid
how do you confirm diagnosis of acute promyelocytic anaemia
cytogenic analysis /FISH /molecular genetic analysis
all the cells look the same as they stopped at same stage of differentiation
what is CD117 a marker of
leukaemia
68 year old with gradual fatigue, lethargy, exertional syncope. pallor, oedema. low neutrophils, low anaemia. Dx?
myelodysplastic syndrome
68 year old with gradual fatigue, lethargy, exertional syncope. pallor, oedema. which is the most important Ix to diagnose?
blood film
what cell is seen in myelodysplastic syndrome
ring sideroblasts
blast cells
72 year old indian woman, veggie, t total. SoB on exertion, fatigue, painful gums/tongue, unable to eat spicy food. pallor. macrocytic anaemia. best Ix?
vitamin b12 and folate
what cell type is classic of pernicious anaemia / megaloblastic anaemia
hypersegmented neurtrophils
tear drop poikilocytes
macrocytes inc oval macrocytes
72 year old indian woman, veggie, t total. SoB on exertion, fatigue, painful gums/tongue, unable to eat spicy food. pallor. macrocytic anaemia. Dx?
megaloblastic anaemia
giant metamyelocyte and megaloblast in BM. Hypersegmented neutrophils. Dx?
pernicious anaemia
70 year old woman with gangrenous toes. No DM, smoker with breathlessness. large spleen. Ix?
blood gas
FBC
70 year old woman with gangrenous toes. No DM, smoker with breathlessness. large spleen. high platelet, high Hb. Dx?
polycythaemia vera
Ix to diagnose polycythaemia vera
molecular analysis for JAK2 mutation
Tx of polycythaemia vera
venesection plus hydroxycarbamide
cause of lymphocytosis in elderly man with no Sx or abnormal blood findings. Dx?
CLL
high RBC, HB and HCt. Dx?
polycythaemia
when polycythmaemia is diagnosed, what question needs to be asked and how is this done?
is this a true or pseudo PC?
check if theres hypoxia / blood loss which can drive up HCt
or bone marrow disease
most likely cause of high WCC in an ICU pt ?
reactive neutrophilia
spanish woman in her 60s with high WCC, normal Hb and splenomegaly. Dx?
CML
spanish woman in her 60s with high WCC, normal Hb and splenomegaly. why is this not AML?
because of normal Hb
elderly man in haematology OPD with bruising and bleeding. low plts, normal everything else. Dx?
immune thrombocytopenia
pale, bruised child. DDx?
NAI
thrombocytopaenia - ALL, immune
haemophillia
causes of microcytosis
iron def
thalassaemia
beta thalassaemia trait blood film results
normal Hb
increased RCC
low MCV
what is a good initial test for ?iron def
ferritin
what blood results are seen in rheumatoid arthritis
anaemia of chronic disease
low neutrophils / platelets due to drug toxicity
felty syndrome
increased ESR
10 year old girl with R painful swollen knee after knocking it. prev fever but afebrile now. High WCC and CRP. DDx?
osteomyelitis
1 year old boy with pain and swelling of joint after minor injury. most likely Dx?
haemophilia
what Ix would you do for haemophilia?
coagulation screen - PT, APTT
coagulation screen results of haemophilia
normal PT
long APTT
red cell fragments
microangiopathic haemolytic anaemia
Dx?
TTP
TTP pentad
microangiopathich haemolytic anaemia
thrombocytopenia
fever
neurological abnormalities
renal impairment
what is the defect in TTP
deficiency of von willebrand factor cleaving protease (ADAMTS13)