haematology: bone marrow Flashcards

1
Q

What is the suffix for increased in blood cell count

A

-cytosis or -phillia

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2
Q

What is the suffix for decreased in blood cell count

A

-cytopenia

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3
Q

What is apoptosis

A

Programmed cell death that is a normal physiological process where old, damaged or unneeded cells are removed from the system

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4
Q

Where do you find bone marrow

A

Central cavities of axial & long bones

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5
Q

What is 3 differences between compact & spongy bone

A

Compact bone:
Dense outer layer
Parallel osteons
Blood vessels
Spongy bone:
Head of long bones
Trabecular with no osteons but osteoblasts,-clast & -cytes
No blood vessels with red & yellow bone marrow

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6
Q

What is the two types of bone marrow & functions

A
  1. Red bone marrow: supplies nutrients to cells in trabeculae & site of haematopoeisis
  2. Yellow bone marrow: stores fat & changes with age (extreme cases can reactivate)
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7
Q

Histology: name the big arrow, arrowhead & long thin arrow

A

image

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8
Q

What does newborns bone marrow consists of mostly

A

Cellular bone marrow

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9
Q

What is aplastic anaemia

A

Body stops producing enough new blood cells

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10
Q

What is the cause of aplastic anaemia

A

Result of bone marrow damage happening at birth or after exposure of radiation & chemotherapy

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11
Q

What is six components of the microenvironment in the bone marrow

A

Osteoblasts: forming bones
Endothelial cells: line blood vessels & passage of cells to bloodstream
Stromal cells: produce ECM
Cytokines: cell-signaling
Adhesion molecules: binds cell to each other & within the matrix
Macrophages: clean up cellular debris

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12
Q

What is the two main functions of bone marrow

A
  1. Haematopoiesis
  2. Immune system
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13
Q

Where is the site of hematopoiesis at different ages

A

Embryo: yolk sac until 6-12 weeks
Fetus: liver & spleen until 2nd trimester
Fetus & adult: bone marrow

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14
Q

When & where does extramedullary hematopoiesis occur

A

Certain disease states
Liver & spleen

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15
Q

What is the three immune function of bone marrow

A
  1. Production of leukocytes
  2. Interaction between leukocytes
  3. Production of cytokines & antibodies
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16
Q

What is cell differentiation

A

Process where immature, undifferentiated cells become more specialise in appearance & function

17
Q

What is the process of cell differentiation

A

Some HSC become quiescence cells while other undergo asymmetrical division. Some cells undergo self-renewal while other undergo differentiation into progenitors cells & become mature cells

18
Q

What is quiescence cells

A

Less vulnerable to harmful insults & in periods of need then exit quiescence cell state

19
Q

What is self renewing cells

A

Some of daughter cell enter cell cycle to divide & differentiate other undergo self-renewal & remain HSC

20
Q

What is cell proliferation

A

Cells divide continuously to form many driven by growth factor & anti-apoptotic signals

21
Q

What is the three mechanisms of bone marrow pathologies

A
  1. Bone marrow infiltrations
  2. Bone marrow failure
  3. Bone marrow suppression
22
Q

What is the three causes & consequences of bone marrow infiltration

A
  1. Hematological malignancies leading to cytopenia
  2. Non-hematological malignancies leading to cytosis
  3. Infections leading to cytopenia
23
Q

What is a cause & consequences of bone marrow failure

A

Aplastic anaemia leading to cytopenia

24
Q

What is a cause & consequences of bone marrow suppressions

A

Drugs, toxins & sepsis leading to cytopenia

25
What is the two examinations regarding bone marrow
1. Bone marrow aspirate 2. Bone marrow trephine
26
What is bone marrow aspirate
Aspirate with 2mL syringe for morphological assessment & 10mL for other tests
27
What is bone marrow trephine
Core biopsy for histological assessment
28
Where does BMA taken from
**Infants:** anterior tibia **Older children & adults:** posterior superior iliac crest of pelvic bones
29
What is four indications of bone marrow examination
1. Bone marrow pathology suspected (malignant or non-malignant) 2. For staging of disease 3. Disease monitoring 4. Rare instance where a diagnosis can not be made by doing peripheral testing