leukaemia and lymphoma Flashcards

1
Q

who does lymphoma tend to affect?

A
  • those aged 16-65, with peak incidence in 30s
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2
Q

what are the symptoms of Hodgkins?

A
  • cervical lymph node enlargement
  • painless, rubbery, contiguous pattern of spread
  • found in axillary and inguinal lymph nodes too
  • hepatosplenomegaly
  • B symptoms: fever (25%), drenching night sweats, weight loss of >10% body weight
  • ## alcohol induced pain at lymph nodes
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3
Q

what symptoms would you expect if you had mediastinal lymph node involvement?

A
  • cough
  • breathlessness
  • SVC obstruction
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4
Q

what cells might you see in hodgkins lymphoma?

what are the risk factors?

A
  • Reed- Sternberg cells
  • infectious mononucleosis (EBV)
  • increased titres of EB antibodies
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5
Q

what is the most common type of HL?

A
  • nodular sclerosing (75%)

- mixed cellularity 25%

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6
Q

what investigations would you do to confirm diagnosis of HL?

A
  • lymph node biopsy

- imaging (CXR or CT scan to check for mediastinal involvement)

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7
Q

what is the staging criteria called and what classes are there?

A

Ann-Arbor staging:

  • 1: confined to single lymph node
  • 2: 2 or more nodes on the same side of diaphragm
  • 3: involvement of nodes either side of diaphragm
  • 4: spread beyond nodes to liver or bone marrow
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8
Q

how else can HL be divided?

A
  • A: absence of symptoms
  • B: symptoms present: weight loss, unexplained fever >38, drenching night sweats
  • survival is <40% for those stage 4B, over 90% for stage 1A
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9
Q

what is non-hodgkins?

A
  • malignant tumour of lymphoid cells
  • 70% are B cell
  • 30% are T cell
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10
Q

what are the core symptoms and signs of non-hodgkins?

how does it differ in presentation to HL?

A
  • peripheral lymphadenopathy (75% have painless superficial lumps)
  • B symptoms
  • extra nodal, more common than HL, can affect brain, lung, liver
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11
Q

what viruses are associated with NHL?

A
  • human T cell lymphocytic virus

- Herpes virus 8 (causes cancer in HIV patients) so HIV an association

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12
Q

what is the pathogenesis?

A
  • malignant clonal expansion of lymphocytes at different stages of development
  • neoplasms of proliferating immature cells (immuno/ lymphoblasts are much more aggressive
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13
Q

what is Burkitts lymphoma?

what is it caused by?

A
  • childhood disease with characteristic jaw lymphadenopathy
  • translocation of oncogene between chromosome 8 and 14
  • results in up regulation of myc
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14
Q

how can burkitts lymphoma be classified?

A
  • low grade: incurable, widely disseminated
  • high grade: more aggressive but long term cure

-30% 5yr survival for low grade, 50% for high grade

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15
Q

what is the peak incidence of leukaemia in children?

A
  • 3 years old in boys
  • 2 years in girls
  • most common cancer in children
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16
Q

what is the most common subtype?

A
  • ALL (78%)
  • AML (15%) <2 years
  • CML
  • CLL
17
Q

what are the risk factors for childhood leukaemia?

A
  • caucasian
  • boys
  • influenza exposure
  • Downs
  • Fanconi’s radiation
18
Q

What is the presentation of leukaemia?

A
  • anaemia symptoms
  • thrombocytopenia
  • hepatosplenomegaly
  • growth restriction and FTT
  • prolonged fever
  • bleeding (gums, bruising)
  • lymph node swelling
  • weight loss, fever
  • cranial nerve lesions
19
Q

what investigations would you do for leukaemia and what would you expect to find?

A
  • Pancytopenia (bone marrow infiltration)

- elevated white cell count (despite neutropenia because all the cells are cancerous)

20
Q

how can childhood leukaemia be staged?

A
  • French-Amrican-British classification widely used in ALL
21
Q

what is the treatment for these cancers?

A
  • high intensity chemotherapy

- imatinib anti-tyrosine kinase therapy in CML

22
Q

what are the potential symptoms of wilms tumour?

what syndromes are associated with it?

A
  • haematuria
  • hypertension
  • Beckwith-Weidemann
  • trisomy 8