W25 - Haem interactive cases Flashcards

1
Q

Myeloblasts may have ________

A

Myeloblasts may have Auer rods

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2
Q

Myeloblasts in BM:

<5% =

5-20% =

>20% =

A

Myeloblasts in BM:

<5% = normal

5-20% = myelodysplasia

>20% = AML

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3
Q

Lymphoblasts in BM:

<5%

>20%

A

Lymphoblasts in BM:

<5% = normal

>20% = ALL

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4
Q

Lymphoblasts are ____ positive

A

Lymphoblasts are TdT positive

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5
Q

TdT is a marker of mature/immature T and B lymphoblasts

A

TdT is a marker of immature T and B lymphoblasts

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6
Q

36 year old woman. History of fatigue, joint pains and with a butterfly/malar rash on face. Also experienced menorrhagia. ESR is 80mm/hr (<15) Bilirubin 32 umol/l (<21)

Write down a likely Haematological diagnosis?

A

Haemolytic anaemia

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8
Q

Spherocytes - autoimmune or inherited. One test to confirm which:

  • Hb electrophoresis
  • DAT (direct antiglobulin)
  • Sickle solubility
  • Unconjugated hyperbilirubinaemia
A
  • DAT (direct antiglobulin)
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9
Q

Spherocytes - when do we see them?

A

hereditary spherocytosis, or

autoimmune haemolytic anaemia which has sphercoytes but is also DAAT +

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10
Q

Inherited haemolytic anaemias - name 4 conditions

A

Membrane: 1) hereditary spherocytosis

Enzymes: 2) G6PD deficiency

Haemoglobin: 3) Sickle cell, 4) Thalassaemia major

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11
Q

A 40-year-old woman of Indian origin, she eats a vegan diet and has five children . She takes regular non-steroidal anti-inflammatory medication for arthritis. She was anaemic on FBCs performed during her pregnancies. Aside from Hb and MCV the remainder of FBC is normal Hb (women)

What is the diagnosis?

A) Iron deficiency anaemia

B) Anaemia of chronic disease

C) Beta thalassemia trait

A

B) Anaemia of chronic disease

= essentially anaemia of (inflammation) chronic disease. ESR raised. but the key to distinguish IDA from ACD is TRANSFERRIN

  • in IDA => transferrin is HIGH
  • in ACD => transferrin is normal/reduced
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12
Q

Acquired haemolytic anaemias - name immune and non-immune conditions

A

Immune: 1) Immune haemolytic anaemia

Non-immune: 2) Malaria, 3) MAHA, 4) drug-induced, 5) HUS, 6) snake bites

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14
Q

59 year-old woman. fatigue. PMH Hypothyroidism and vitiligo

Chose the most likely diagnosis?

A) Folate deficiency

B) Autoimmune haemolytic anaemia

C) B12 deficiency

D) Acute leukaemia

A

Hb low, MCV very high, WCC low, neutrophils low, platelets low

C) B12 deficiency = she likely has pernicious anaemia (hence not folate)

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15
Q

59 year old man. Pharyngitis not responded to antibiotics, Recurrent nose bleeds. fatigue, difficulty passing urine and haematuria

Interpret bloods and blood film. What is the most likely haematological diagnosis?

A

Hb low, MCV normal, WCC low, neurophil low, platelets low = pancytopaenia

Peripheral blood film: nucleated RBcs, myelocytes (immature cell which should be in BM, not in peripheral blood), tear drop cell

= leuko-erythroblastic picture due to BM infiltration either by 1) blood cncer, 2) metastatic cancer

this is likely prostate cancer metastasized to BM

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16
Q

How to distinguish ACD from IDA on blood test?

A

Transferrin (which is essentially TIBC)

IDA => transferrin is HIGH

ACD => transferrin is LOW/NORMAL

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17
Q

Interpret bloods, peripheral blood film, and come up with signle most useful test.

A

bloods: WCC VERY HIGH, neutrophil count VERY HIGH, rest is normal

blood film: lots of neutrophils, some basophils, some myelocytes

likely CML = check for Ph chromosome = BCR-ABL ASSAY

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18
Q

Why is iron low in ACD?

A

ACD = anaemia of inflammation => hepcidin levels are high in inflammation => high hepcidin inhibits GP asborption of iron + sequesters Fe in macrophages and Kupffer cells (as a means to remove available iron for invading bacteria)

21
Q

Interpret results. What treatment would you give?

A

CML that has now entered blast phase => TKI that works directly to inhibit ABL =>

imatinib

22
Q

What is the likely haematological diagnosis at month 60?

A

Blast crisis => disease has gone from CML to AML (blast cell 25% in peripheral blood)

23
Q

Single most useful test to confirm the likely haematological diagnosis?

A

JAK2-V617F mutation

24
Q

Peripheral blood leucocyte immunophenotyping is performed.

What is the likely diagnosis? What test is most useful?

A) DAT

B) Immunophenotyping for CD19/CD5/CD3 expression

C) HTLV1 serology

D) BCR-ABL assay

E) JAK2-V617F mutation analysis

F) Factor V leiden screen

A

high WCC, high lymphocytes = likely CLL

B) Immunophenotyping for CD19/CD5/CD3 expression

25
Q

Pancytopaenia

name non-malignant (2) and malignant (2) causes

A

Pancytopaenia

non-malignant (2):

  1. DNA synthesis failure (B12 or folate)
  2. Aplastic anaemia

malignant (2):

  1. metastatic non-haem cancer (i.e. breast)
  2. haem cancer infiltrating BM (i.e. leukaemia, myeloma, lymphoma)
27
Q

Write down the likely underlying diagnosis ?

A

Hb low, calcium high, IgA very high with suppression of IgM and IgG

Multiple myeloma

NB: A mid-femur fracture in a 59 year old man is either due to 1) trauma, or 2) cancer spread to bone or 3) MM.

28
Q

CML - common symptoms and signs

A

CML history: lethargy/hypermetabolism/thrombotic event (monocular blindness CVA) bruising, bleeding

CML exam: massive splenomegaly +/- hepatomegaly

29
Q

Most likely cause of renal failure?

A

Cast nephropthy

Cast nephropathy are depositions of free light chains depositing and blocking off nephrons

This patient has sky high levels of free light chains – these pass through BM of kidney and may precipitate renal failure

30
Q

CML - common FBC and blood film findings

A
  • Hb and platelets well preserved or raised
  • Massive leucocytosis 50-200x109/L
  • Blood film: Neutrophils and myelocytes (not blasts if chronic phase), Basophilia
31
Q
The \_\_\_\_\_\_\_ translocation produces
the Philadelphia (Ph) chromosome which expresses...
A
The **t(9;22)** translocation produces
the Philadelphia (Ph) chromosome which expresses **a fusion oncoprotein with TK acitvity driving myeloid proliferation**
36
Q

CLL - name 3 cell based prognostic factors.

A
  1. IgHV mutation status
  2. CLL FISH cytogenetic panel
  3. TP53 mutation status (Chromosome 17p del and/or TP53 point mutation) *most imp
37
Q

Which 2 drug are used in treatment of CLL?

A
  1. Ibrutinib (Briton tyrosine kinase inhibitor)
  2. Venetoclax (BCL2 inhibitor)
39
Q

MM - Define CRAB

A

Calcium

Renal failure

Anaemia

Bone disease