Haematology Flashcards

1
Q

What are the main causes of lymphadenopathy?

A
  1. Infectious
    - viruses: EBV, CMV, HIV, hepatitis, HSV, rubella
    - bacteria
    - fungi
    - parasites
  2. Malignant disorders
    - primary haematological disorders: lymphoma, myeloid disorders
    - solid tumour metastases
  3. Disorders with immunological mechanism
    - autoimmune disorders: SLE, RA, vasculitis
    - sarcoidosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the main causes of splenomegaly?

A
  1. Haematological disorders:
    - haemolysis
    - thalassaemia major and intermedia
    - sickle cell anaemia
    - haemolytic anaemia
  2. Malignancies
    - lymphomas
    - leukaemias
    - myeloma
    - metastases of solid tumours
  3. Inflammation
    - sarcoid
    - serum sickness
    - SLE, RA
  4. Infection
    - viral: hepatitis, EBV, CMV
    - bacterial
    - parasitic: malaria, schistosomiasis, toxoplasmosis
    - infective endocarditis
    - fungal
  5. Congestive
    - cirrhosis
    - heart failure
    - thrombosis of portal, hepatic or splenic veins
  6. Non-malignant, infiltrative:
    - Niemann-Pick disease
    - amyloid
    - glycogen storage disease
    - Gaucher’s disease
    - Haemophagocytic lymphohistiocytosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the three major types of anaemia and what are their causes?

A
  1. Microcytic hypochromic anaemia
    - iron deficiency
    - thalassaemia
  2. Normocytic normochromic anaemia
    - acute bleeding
    - haemolysis
    - marrow infiltration
    - anaemic of chronic disease (esp. CKD)
  3. Megaloblastic or macrocytic
    - B12/folate deficiency
    - alcoholism
    - liver disease
    - hypothyroidism
    - myelodysplasia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Where are the palpable lymph nodes?

A
  1. cervical
  2. supraclavicular
  3. axillary
  4. inguinal
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Where are the non-palpable lymph nodes?

A
  1. hilar
  2. mediastinal
  3. abdominal/retroperitoneal
  4. generalised lymphadenopathy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are the common causes of cervical lymphadenopathy?

A
  • bacterial infection
  • EBV, rubella, TB
  • lymphoma (frequently unilateral)
  • head-neck tumours (frequently unilateral)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are the common causes of axillary lymphadenopathy?

A
  • bacterial infection
  • lymphoma
  • breast cancer
  • melanoma
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are the common causes of supraclavicular lymphadenopathy?

A
  • lung, retroperitoneal or gastrointestinal tumours
  • lymphoma
  • chest or retroperitoneal bacterial or fungal infection
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are the common causes of inguinal lymphadenopathy?

A
  • bacterial infections of lower extremity, genitals or perianal regions
  • pelvic tumours, lymphoma
  • venereal diseases (lymphogranuloma venereum, syphilis)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

How is lymphoma broadly categorised?

A

Divided broadly into:

  1. Hodgkin’s lymphoma
  2. Non-Hodgkin’s lymphoma
    - indolent lymphoma (follicular lymphoma, CLL/SLL, MCL, MZL)
    - aggressive lymphoma (diffuse large B cell lymphoma)
    - very aggressive lymphoma (Burkitt’s lymphoma and Acute Lymphoblastic Lymphoma)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the principles of treatment for lymphomas?

A
  1. Low grade lymphoma
    - not curable
    - only treat if there is indication to treat
    - exception: need to treat MCL, follicular lymphoma may be curable with radiotherapy
  2. High grade lymphoma
    - curable
    - always treat DLBCL
  3. Burkitt’s or ALL:
    - very curable
    - MUST treat, otherwise fatal
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What methods are used to diagnose lymphoma?

A
  1. Histology
    - look at tissue biopsy down a microscope (FNA is not diagnostic)
    - architecture
    - morphology (small cells = low grade; large cells = high grade)
  2. Flow cytometry or immunohistochemistry
    - look for cell surface markers
  3. Cytogenetics
    - particular genes are either diagnostic or prognostic for lymphoma
    - detects deletions, translocations, etc.
  4. Molecular PCR
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What symptoms might you find on history and examination of a patient with lymphoma?

A
  1. Symptoms of proliferation:
    - B symptoms: weight loss, drenching night sweats, recurrent fever
  2. Symptoms related to organ damage or mechanical obstruction
    - specific organ damage
    - large lymph nodes
  3. Symptoms associated with bone marrow failure
    - anaemia: tiredness, postural hypotension, SOB, pale sclera, tachycardia
    - recurrent infections
    - bleeding, bruising
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the two categories of multiple myeloma?

A
  1. Smouldering MM
    - criteria for MM has been met (para-protein >30grams/L or bone marrow plasma cells >10%) but the disease is quiescent
    - defined by lack of end organ damage
    - no evidence that treatment will prolong survival
    - treat small group: MM with positive biomarkers
  2. Active MM
    - defined by end organ damage: CRAB
    - C: hypercalcaemia due to cytokines causing bone resorption
    - R: renal damage due to hypercalcaemia and light chain toxicity
    - A: anaemia due to bone marrow invasion
    - B: bone pain due to cytokines causing bone resorption
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What proportion of smouldering MM patients are treated?

A

MM with positive biomarkers are treated.

  • defined as myeloma with MRI lesions
  • do not have active disease but benefit from treatment
  • if patient is found to have smouldering MM, need to consider MRI scan for detection of positive biomarkers
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What are the principles of treatment for MM? (goals, who to treat, how to treat)

A

Note: MM is not curable but very treatable

Goals of treatment:

  • treat disease itself
  • prevent end organ damage

Two populations require treatment:

  1. active MM
  2. MM with positive biomarkers

If a patient requires treatment, there are two options:

  1. Eligible for autologous stem cell transplants
    - patients <65 yo, no significant co-morbidities
    - induction therapy with Bortezomib + Lenalidomide
    - high dose ablative chemotherapy then ‘rescue’ with SC transplant
    - followed by maintenance therapy
  2. Ineligible for SC transplant
    - people >75 yo or with significant comorbidities
    - ongoing Bortezomib + Lenalidome