Blood Flashcards

1
Q

iron deficiency anaemia type of anaemia

A
  • Small - low MCV (microcytic)
  • Pale - low MCH (hypochromic)
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2
Q

predisposing factors to iron deficiency anaemia

A
  • Increased iron loss
    • GI bleed
    • Menstruation
    • Drugs: NSAIDs, Aspirin, Blood thinners
  • Increased iron requirement
    • Pregnancy
  • Decreased intake or malabsorption
    • Vegetarians (insufficient red meat)
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3
Q

thalassemia type of anaemia

A
  • Small - low MCV (microcytic)
  • Pale - low MCH (hypochromic)
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4
Q

vitamin B12/folate deficiency type of anaemia

A

macrocytic megaloblastic anaemia

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5
Q

predisposing factors to b12 deficiency anaemia

A

Strict vegans, Inherited B12 receptor deficiency, Coeliac, Crohn’s disease

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6
Q

lymphoma clinical symptoms

A
  • Enlarging masses at sites of lymphoid tissue
    • Typically painless
  • Interference with normal organ function
  • Systemic symptoms
    • Fever
    • Night sweats
    • Weight loss (>10% of body weight)
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7
Q

aggressive vs indolent lymphomas character and prognosis

A
  • Aggressive
    • Character
      • High proliferation & high apoptosis rate, large
        proliferation margin
      • More often localised at presentation than indolent
    • Prognosis
    • Shorter natural history, median survival ≤ 2 years
    • Curable disease in some if aggressive therapy is
      started
    • All childhood lymphomas are of this type
  • Indolent
    • Character
      • Low proliferation & death rate, small proliferation
        margin
    • Often widespread at diagnosis
  • Prognosis
    • Prolonged natural history, median survivals > 5 years
    • Currently incurable unless it is a localised disease or
      through marrow ablation with some type of HSC
      Transplant
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8
Q

diffuse large B cell lymphoma (DLBCL) clinical features

A
  • Aggressive Lymphoma
  • Most common Lymphoma
  • Disease of adults and children, but median age 64
  • Presentation: rapidly enlarging masses
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9
Q

diffuse large B cell lymphoma (DLBCL) morphology

A
  • Diffuse infiltration of lymph node
  • Large lymphoid cells
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10
Q

Burkitt Lymphoma type and morphology

A
  • Aggressive lymphoma
  • starry sky pattern at low power
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11
Q

Follicular lymphoma type and epiD

A
  • indolent lymphoma
  • most common type of indolent lymphoma, second most common type of lymphoma
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12
Q

follicular lymphoma morphology

A

Retains characteristic follicular structure

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13
Q

Hodgkin vs non-Hodgkin lymphoma characteristics, morphology and associations

A

Hodgkins:
Localized, single group of nodes with contiguous spread
Better prognosis
Characterized by Reed-Sternberg cells
More common in young adulthood and > 55 years
Associated with EBV

Non-Hodgkins:
Multiple lymph nodes involved, extranodal involvement common
Non-contiguous spread
Worse prognosis
Majority involve B cells; few of T cell lineage
Can occur in children and adults

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14
Q

leukemia epiD

A

Leading cause of cancer death in children under 15 years of age

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15
Q

acute leukemia clinical features

A
  • Symptoms resulting from suppression of normal marrow function
    - Few RBCs → Anaemia, with accompanying fatigue
    - Neutropenia → Fever, usually reflecting an
    infection
    - Thrombocytopenia → Bleeding
    • Usually fatal within weeks if left untreated
    • Characterised by presence of immature, blast cells
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16
Q

chronic leukemia clinical features

A
  • Non-specific symptoms
    • Fatigue, Weight loss, Anaemia
  • Patients with untreated Chronic leukemia usually survive much longer
  • Usually associated with more mature and well-differentiated cells
17
Q

ALL (Acute Lymphoblastic Leukemia) epiD

A
  • Rare (1/100 000 per year)
  • Mostly a childhood disease, with a peak incidence at age 3
18
Q

AML (Acute Myelogenous Leukemia) epiD

A
  • Rapidly fatal without treatment
  • More common in adults than children
19
Q

CLL (Chronic Lymphocytic Leukemia) epiD

A
  • Represents approximately 1/3 of all leukemias
    • CLL is primarily a disease of the elderly, median age of onset being 65 years
20
Q

CML (Chronic Myeloid Leukemia) epiD

A
  • Usually a disease of middle age, although it may occur in children and young adults
    • Usually presents in an indolent chronic phase, which may last several years
    • Invariably progresses from the chronic phase to an accelerated and acute phase, lasting 0.5 to 2 years