Haem Flashcards

1
Q

Management of Heparin-Induced Thrombocytopenia (HIT)

A

Switch to argatroban or danaparoid

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

Indication for treatment in CLL

A

Constitutional symptoms

Bone marrow failure

Symptoms due to LN/spleen/liver elargement

Weight loss > 10% in 6 months

AI anaemia/ thrombocytopenia not responding to prednisolone

Lymphocyte doubling in <6m, or 50% increase in 2m

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

Indication for use of Ibrutinib (BTK inhibitor) in CLL

A

TP53 mutation

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

Pentad of features in TTP (Thrombotic Thrombocytopenic Purpura)

A
  1. Thrombocytopenia
  2. MAHA (anaemia + schistocytes)
  3. Fever
  4. Fluctuating neuro signs
  5. Renal impairment
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Causes of MAHA (schistocytes seen on film)

A

TTP
HUS
DIC
Pre-eclampsia

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

Presentation of HUS

A

Haemolytic anaemia (MAHA)
Thrombocytopenia
Severe AKI
Following bloody diarrhoea

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

AL amyloidosis presents as

A

Nephrotic syndrome
Cardiomyopathy
Peri-orbital purpura
(Macroglossia)
(Urine free light chains)
Without features of MM

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

Waldenstrom’s macroglobulinaemia (lymphoplasmacytoid malignancy) presents as

A

Monoclonal IgM paraproteinaemia
Hyperviscosity
Systemic upset

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

Commonest initial treatment for CLL

A

Fludarabine + cyclophosphamide + rituximab (FCR)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Other options for CLL treamtent, when FCR not appropriate

A

Bendamustine
Chlorambucil
Anti-CD20 (obinutuzumab)

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

Management of AI anaemia/thrombocytopenia in CLL

A

Prednisolone

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

Treatment of Waldenstrom macrogolubulinaemia

A

Cyclophosphamide + dexamethasone + rituximab

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

Features of monoclonal gammopathy of unknown significance (MGUS)

A

Paraproteinaemia
Asymptomatic/neuropathy
Normal immune function
No bone lesions/renal impact

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Schnitzler’s syndrome

A

Chronic urticaria
Monoclonal raised IgM

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

Features of methaemoglobinaemia

A

Cyanosis
Low O2 sats with normal PaO2
Ischaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

R-CHOP is

A

Rituximab
Cyclophosphamide
Doxorubicin
Vincristine
Prednisolone

17
Q

Management of NHL - low-grade and asymptomatic

A

Watch and wait

Vaccinate (flu, haemophilus, pneumococcus, meningococcus)

18
Q

Chemo options for NHL

19
Q

Management of primary CNS lymphoma

A

High-dose methotrexate + dexamethasone

20
Q

Imatinib is chemotherapy agent used in

A

CML
MALT-lymphoma
c-kit melanoma

21
Q

Non-Hodgkins Lymphoma with CNS involvement

A

R-CHOP + intrathecal methotrexate

22
Q

Curative treatment for myelofibrosis

A

Allogenic stem-cell transplant

23
Q

Drugs used in control of myelofibrosis

A

Hydroxyurea
IFN-a
JAK inhibitors

24
Q

Diagnostic criteria for HHT (Osler-Weber-Rendu)
Need 3 for definite diagnosis.

A

Epistaxis
Telangiectasia
AVMs or GI telangiectasia
1st-degree family history

25
Impaired platelet aggregation with Ristocetin, suggests
von Willebrand's disease
26
BCR-ABL mutation is diagnostic for
CML
27
BCL2 mutation seen in
Diffuse large B cell lymphoma
28
TP53 mutation seen in
Diffuse large B cell lymphoma
29
C-MYC mutation seen in
Burkitt's lymphoma
30
Commonest mutation seen in myelofibrosis
JAK2
31
Lysosomal storage disorder which causes massive splenomegaly
Gaucher disease
32
Lysosomal storage disorder which causes massive splenomegaly
Gaucher disease
33
Causes of warm AIHA
Autoimmune (eg SLE) CLL, lymphoma Methyldopa
34
Causes of cold AIHA
Mycoplasma EBV Lymphoma
35
Prophylactic antimicrobials given when starting chemotherapy (FCR)
Co-trimoxazole Aciclovir Fluconazole
36
CLL - Poor prognostic factors (median survival 3-5 years)
Male >70yo Lymphocyte count >50 Polymorphs >10% Doubling time <12m Raised LDH CD38 positive TP53 mutation