White cell disorders: investigation of neutropenia, leukaemia and leukaemoid reactions Flashcards

1
Q

Types of WBC

A

Granulocytes:

  • neutrophils
  • basophils
  • eosinophils

Lymphocytes:

  • B cells
  • T cells

-monocytes (and macrophages)

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2
Q

function of neutrophils

A

chemotaxis, phagocytosis, killing of phagocytosed bacteria

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3
Q

function of basophils

A

Mediate immediate type hypersensitivity (IgE), modulate inflammatory responses by releasing heparin and proteases

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4
Q

function of eosinophils

A

All neutrophil functions (chemotaxis, phagocytosis, killing of phagocytosed bacteria) as well as antibody dependent damage to paracites, regulate immediate type hypersensitivity reactions (inactivating histamine and leukotrienes released by basophils and mast cells)

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5
Q

function of B cells

A

B Cells: 10-30%: effectors of humoral immunity –i.e. Antibody production
40% IgM , 30% IgD, 30% IgG and 10% IgA
kappa light chain or lamda light chain (normal ratio 2:1)
Activated B cells develop into plasma cells

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6
Q

function of T cells

A

grade intracellular pathogens such as mycobacteria.
Interaction with B cells in producing antibodies against certain antigens
Participation in delayed hypersensitivity reactions

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7
Q

function of monocytes and macrophages

A

Chemotaxis, phagocytosis, killing of some micro organisms, antigen presentation and modulation of inflammatory response

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8
Q

causes of neutrophilia

A

-bacterial infection
-inflammation
-drugs/medication- commonly caused by steroids (cause neutrophilia and lymphopenia),
-primary haematological malignancy e.g. acute leukaemia
-dietary e.g. B12, folate, copper
-pregnancy
-lactation
-exercise
-neonates
-burns
-rheumatoid arthritis
-vasculitis
0MI
-uraemia
-DKA
-smoking

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9
Q

define leukaemia

A

blood cancer derived from the bone marrow

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10
Q

causes of congenital neutropenia

A
  • constitutional
  • ethnic e.g Afro-Carribean and Chinese have lower normal neutrophil count compared to Caucasian popoluation
  • severe congenital neutropenia
  • cyclic neutropenia
  • Fanconi anaemia
  • Chediak-Higashi
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11
Q

how to investigate a neutropenic patient

A

-Age
-History: Infections, drug exposure, autoimmunity
B symptoms/bleeding
-Family History
-Examination: Syndromic features, infection, skin, changes/arthropathy, hepatosplenomegaly, lymphadenopathy
-Investigations: FBC,
Blood film, Haematinics, viral screen, TFTs, autoimmune screen
Second line
Chest xray
USS abdomen
Bone marrow biopsy

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12
Q

leukaemia investigations

A
FBC
U&Es/LFTS/CRP
Coagulation
Virology
Blood film
Bone marrow
morphology, immunophenotyping, Cytogenetics, molecular analysis
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13
Q

define leukocytosis

A

increase in total white cell count

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14
Q

describe white cell changes in inflammation

A
  • Neutrophilia with toxic granulation and left shift secondary to accelerated neutrophil production
  • Usually accompanied by raised PLT
  • Leukaemoid reaction: WBC>50,000/microLfrom causes other than leukemia,; mature neutrophils; accompanied by increased numbers of bands, metamyelocytes,and/ormyelocytes
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15
Q

causes of neutropenia

A
  • drugs e.g. chemotherapy, antipsychotics- clozapine, antibiotics
  • viral infections e.g. HIV, dengue fever
  • splenomegaly
  • autoimmune
  • dietary e.g. B12 or folate deficiency
  • BM infiltration
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