Haematology Flashcards

Anaemia B12 Deficiency Chemotherapy Clotting Disorders Immunocompromised Fever Leukaemia Bleeding Tendency Iron Deficiency Myeloma Recurrent Thrombosis Thrombocytopenia Haemophilia A (X) Thalassaemia

1
Q
  1. Define anaemia.
  2. When is a patient considered anaemic?
A
  1. Decrease RBC which is detected by [Hb]
  2. Adults: M < 130g/L & F < 120g/L
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2
Q

What symptoms and signs will you ask/look for in an anaemic patient? What additional things will you ask for in history?

A

Symptoms: fatigue, SOB, headache, palpitations, syncope

Signs: pale conjunctiva + palmer creases + mucosal membranes, tachycardia

History: diet? menstrual cycle? alcohol? family history?

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3
Q

What are 3 causes of microcytic anaemia?

A

Microcytic (<80):

  1. iron deficiency anaemia
  2. thalassemia
  3. sideroblastic anaemia
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4
Q

What are 3 causes of normocytic anaemia?

A

Normocytic (80-100):

  1. acute blood loss (GI/GU)
  2. anaemia of chronic disease
  3. sickle cell disease
  4. multiple myeloma
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5
Q

What are 3 causes of macrocytic anaemia?

A

Macrocytic (>100):

  1. B12 or folate deficiency
  2. drugs that impair DNA synthesis (e.g. methotrexate)
  3. alcoholism (or liver disease)
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6
Q

What investigations do you run to identify the type of anaemia?

A
  1. FBC with MCV & RDW
  2. reticulocyte count
  3. blood film
  4. vitamin B12 and folate
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7
Q

Do anaemic patients need a transfusion? What other treatments are there?

A

Usually not, it depends on how severe the anaemia is (when Hb <70g/mL). Typically, iron supplements are a safer and less costly method to raise Hb levels.

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8
Q

In what foods in vitamin B12 found and how much does the body store?

A
  • Found in meat, fish and dairy products, but not in plants
  • Body stores up to 4 years worth
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9
Q

What are the causes of vitamin B12 deficiency anaemia?

A
  • Diet: vegan - Malabsorption: Crohn’s disease, ileum resection, tapeworms, gastritis - Genetics: transcobalamin II deficiency (congenital abnormality in metabolism)
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10
Q

Where is folate and vitamin B12 absorbed?

A

Jejunum and ileum respectively

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11
Q

How is vitamin B12 absorbed into the body?

A

Vitamin B12 binds to intrinsic factor that is secreted by gastric parietal cells. B12-IF complexes protects B12 from other enzyme degradation. Later absorbed in terminal ileum and binds to transcobalamin.

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12
Q

What are the clinical features of vitamin B12 deficiency?

A

Symptoms of anaemia Neurological symptoms (some reversible and irreversible) - cerebral (reversible): dementia, delirium, confusion - cord (irreversible): subacute combined degeneration - peripheral neuropathy

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13
Q

What is the pathophysiology of pernicious anaemia?

A

Auto-Ab produced against gastric parietal cells leading to achlorhydria (absent or low gastric acid secretions) and lack of IF i.e. an autoimmune disorder resulting in vitamin B12 deficiency which is common in >60yo.

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14
Q

What test can you run to distinguish pernicious anaemia from other causes?

A

Schilling test - basically tracing radio-labelled B12 and measuring the urinary excretion

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15
Q

What is the treatment of pernicious anaemia?

A

Vitamin B12 injections (IM, 1000ug) monthly for life

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16
Q

Define leukaemia, lymphoma and myeloma.

A
  • Leukaemia = malignant cells arising in bone marrow - Lymphoma = malignant cells arising in lymph nodes and lymphoid tissues - Myeloma = malignant plasma cells which collect on the outer part of bones forming tumours i.e. multiple myeloma
17
Q

What are B symptoms?

A
  1. Fever > 38C (Pel-Ebstein fever is associated with Hodgkin Lymphoma) 2. Drenching night sweats 3. Unintentional weight loss >10% in <6 months
18
Q

What is used to stage lymphomas?

A

Ann Arbor System of Staging Lymphoma (also used for prognosis): Given a stage I-IV and a subtype A or B. I = confined to singly lymph node region II = involvement of 2+ lymph nodes on same side of diaphragm III = involvement of lymph nodes on both sides of diaphragm IV = spread beyond lymph nodes e.g. liver or bone marrow A = absence of B symptoms B = presence of B symptoms

19
Q

How is Hodgkin Lymphoma distinguished from Non-Hodgkin Lymphoma?

A

Presence of Reed-Sternberg cells.

20
Q

What are the risk factors of Hodgkin’s Lymphoma?

A
  • EBV or HIV infection - age: 20’s and >55 - M > F - caucasian > asian
21
Q

Are low-grade lymphomas more treatable or high-grade lymphomas? And what are examples of each?

A

High-grade (acute): they are more aggressive but long-term cure is achievable e.g. Burkitt’s lymphoma, DLBCL Low-grade (chronic): they are indolent but often incurable e.g. follicular lymphoma

22
Q

What is the type of chemotherapy is used for Non-Hodgkin’s and Hodgkin’s Lymphoma?

A

HL = ABVD (Adriamycin, Bleomycin, Vinblastine, Dacarbazine) NHL = R-CHOP (Rituximab Cyclophosphamide, Hydroxydaunorubicin, Oncovin & Prednisolone)

23
Q

What is the name of a rare stem cell disorder leading to pancytopenia (reduction in all major cell lines) and hypoplastic marrow (the marrow stops making cells)?

A

Aplastic anaemia

24
Q

What are the symptoms of myeloma?

A

Calcium (increased) (due to increased osteoclast activity) Renal impairment & Recurrent bacterial infections Anaemia Bone lesions (typically long bones, ribs, vertebra causing back pain)

25
Q

If you suspect myeloma, what investigations should you run and what will they show?

A
  1. FBC: normocytic, normochromic anaemia 2. Blood film: rouleaux formation 3. ESR, urea, Cr, Ca: increased 4. Serum and urine electrophoresis: monoclonal protein band 5. CXR: lytic ‘punched-out’ lesions e.g. pepper-pot skull, vertebral collapse, fractures or osteoporosis