Haematological Malignancy Flashcards

(37 cards)

1
Q

haematological malignancies account for what percent of all human cancers?

A

10%

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2
Q

do blood cancers occur more often in men or women?

A

adult males

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3
Q

what is the most common cancer among children aged 0-14?

A

leukaemia

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4
Q

leukaemia makes up what percent of all childhood cancers?

A

30%

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5
Q

what is the most common form of leukaemia in children?

A

acute lymphocytic leukaemia

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6
Q

myeloid malignancies arise from what cells?

A
RBC
Platelets
Neutrophils
Eosinophils
Basophils
Monocytes
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7
Q

lymphoid malignancies arise from what cells?

A

B-cell

T-cell

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8
Q

using a diagram describe leukaemia vs lymphoma

A

see notes

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9
Q

name the major groups of haematological malignancies

A
acute leukaemia's
chronic leukaemia's
malignancy lymphomas
multiple myeloma
myelodysplastic syndromes (MDS)
chronic myeloproliferative disease (biologically malignant)
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10
Q

name acute leukaemia’s

A

acute lymphoblastic leukaemia (ALL)

acute myeloid leukaemia (AML)

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11
Q

name chronic leukaemia’s

A
chronic myeloid leukaemia (CML)
chronic lymphocytic (CLL)
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12
Q

name the malignancy lymphomas

A
Non-Hodgkin lymphomas (NHL)
Hodgkin lymphoma (HL)
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13
Q

describe the features of acute leukaemia

A

leukaemic cells do not differentiation
bone marrow failure
rapidly fatal if untreated
potentially curable

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14
Q

describe the features of chronic leukaemia

A

leukaemic cells retain the ability to differentiate
proliferation without bone marrow failure
survival for a few years
not presently curable without BMT

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15
Q

clinical features of acute leukaemia

A

bone marrow failure
anaemia
thrombocytopenic bleeding
infection because of neutropenia

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16
Q

what is the most likely cause of infection acute leukaemia?

A

bacterial and fungal

17
Q

essential investigations in acute leukaemia

A
  • Blood count and blood film
  • Bone marrow aspirate/trephine
  • Cytogenetics of leukemic blasts
  • Immunophenotyping of leukemic blasts
  • CSF examination if symptoms
18
Q

treatment of AML

A
  • Supportive care
  • Anti-leukemic chemotherapy
  • Stem cell transplantation – allogenic
  • All trans retinoic acid in APL
19
Q

clinical features of chronic myeloid leukaemia

A
•	Anaemia
•	Splenomegaly, often massive
•	Weight loss
•	Hyperleukocytosis – fundal haemorrhage and venous congestion, altered consciousness, respiratory failure
Gout
20
Q

laboratory features of CML

A
  • High WCC (can be very high)
  • High platelet count
  • Anaemia
  • Blood film shows all stages of white cell differentiation with increased basophils
  • Bone marrow is hypercellular
  • Bone marrow and blood cells contain the Philadelphia chromosome t(9,22)
21
Q

treatment of CML

A

• Tyrosine Kinase Inhibitors
o Imatinib (Gilvec), Dasatinib (Sprycel), Nilotinib (Tasigna), Busitinib, Ponatinib
• Direct inhibitors of BCR-ABL is first line
• Allogenic transplantation – only in TKI failures

22
Q

what are myelodysplastic syndromes?

A

acquired clonal disorders of the bone marrow

23
Q

who gets myelodysplastic syndromes?

A

often old age

24
Q

what do myelodysplastic syndromes present as?

A

macrocytic anaemia

pancytopenia

25
wht are myelodysplastic syndromes fatal?
result of progression to bone marrow failure of AML
26
treatment of myelodysplastic syndromes
supportive or stem cell transplantation for the few young patients
27
give 3 examples of myeloproliferative diseases
* Polycythaemia vera * Essential thrombocythemia * Idiopathic myelofibrosis
28
where are B cells found in lymph nodes?
follicles
29
where are T cells found in lymph nodes?
paracortex
30
where are plasma cells found in lymph nodes?
medulla
31
where in the lymph node do cells undergo expansion and selection?
germinal centre
32
where in the lymph node are naive cells found?
mantle zone
33
presentation of the lymphomas
• Nodal disease – lymphadenopathy o >90% HL o ~60% present purely with nodal disease • Extranodal disease o ~40% NHL present with an extranodal component • Systemic symptoms o Fever, drenching sweats, loss of weight, pruritis, fatigue
34
causes of lymphadenopathy: localised and painful
bacterial infection in drainng site
35
causes of lymphadenopathy: localised and painless
rare infections, catch scratch fever, TB metastatic carcinoma from draining site - hard lymphoma - rubbery reactive, no cause identified
36
causes of lymphadenopathy: generalised and painful/tender
viral infections: EBV, CMV, hepatitis, HIV
37
causes of lymphadenopathy: generalised and painless
``` lymphoma leukaemia connective tissue diseases, sarcoidosis reactive, no cause identified drugs ```