Hematologic & Immune Disorders Flashcards

Covers hemostasis, blood cell disorders, hypersensitivity, autoimmune diseases, and transplant immunology. (25 cards)

1
Q

What is hemostasis?

A

The process that prevents excessive bleeding while maintaining blood flow in circulation, involving vasoconstriction, platelet plug formation, and coagulation cascade activation.

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2
Q

What are the three phases of hemostasis?

A

1) Vascular phase – Immediate vasoconstriction to reduce blood loss.

2) Platelet phase – Platelets adhere to damaged endothelium, forming a plug.

3) Coagulation phase – Activation of clotting factors leads to fibrin clot formation.

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3
Q

What is the difference between primary and secondary hemostasis?

A
  • Primary hemostasis: Platelet adhesion, activation, and aggregation forming a temporary plug.
  • Secondary hemostasis: The coagulation cascade stabilizes the plug with fibrin​.
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4
Q

What is Disseminated Intravascular Coagulation (DIC)

A

A life-threatening condition where excessive clotting depletes clotting factors and platelets, leading to simultaneous thrombosis and hemorrhage.

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5
Q

What causes Disseminated Intravascular Coagulation (DIC)

A

Sepsis (most common cause)

Trauma, burns, obstetric complications, cancer, severe infections​

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6
Q

What are the lab findings in DIC ( Disseminated Intravascular Coagulation)?

A

↑ D-dimer (due to fibrin breakdown)

↓ Platelet count

↑ PT and aPTT (prolonged clotting times)

↓ Fibrinogen levels​

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7
Q

What is the treatment for DIC (Disseminated Intravascular Coagulation)?

A

Treat underlying cause, supportive therapy (platelet transfusion, fresh frozen plasma), anticoagulants (heparin in some cases)

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8
Q

What is thrombocytopenia? (Low Platelet Count)

A

A platelet count < 150,000/µL, leading to increased bleeding risk

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9
Q

What are common causes of thrombocytopenia? (Low Platelet Count)

A
  • Bone marrow suppression (chemotherapy, leukemia)
  • Immune destruction (ITP, heparin-induced thrombocytopenia)
  • Splenic sequestration (liver disease, splenomegaly)​
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10
Q

What are signs of thrombocytopenia? (Low Platelet Count)

A

Petechiae, purpura, mucosal bleeding, prolonged bleeding time​.

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11
Q

What is thrombocytosis? (High Platelet Count)

A

A platelet count > 450,000/µL, increasing the risk of thrombosis.

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12
Q

What are causes of thrombocytosis? (High Platelet Count)

A
  • Primary (essential thrombocythemia) – Bone marrow overproduction.
  • Secondary (reactive thrombocytosis) – Infections, inflammation, iron deficiency​
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13
Q

What is neutropenia? (Low Neutrophils)

A

Absolute neutrophil count (ANC) < 1,500/µL, increasing infection risk​.

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14
Q

What causes neutropenia? (Low Neutrophils)

A
  • Bone marrow failure (chemotherapy, leukemia)
  • Autoimmune disorders
  • Severe infections depleting neutrophils​
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15
Q

What is leukopenia? (Low WBCs)

A

A total WBC count < 4,000/µL, often caused by bone marrow failure or viral infections​

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16
Q

What is leukocytosis? (High WBCs)

A

A total WBC count > 11,000/µL, usually due to infection, inflammation, or leukemia.

17
Q

What is polycythemia?(Increased RBC Count)

A

Excess RBCs, leading to increased blood viscosity and clot risk

18
Q

What are the two types of polycythemia? (Increased RBC Count)

A

1) Primary polycythemia (Polycythemia Vera) – Bone marrow disorder causing excessive RBC production.

2) Secondary polycythemia – Due to chronic hypoxia (e.g., COPD, high altitude)​

19
Q

What are the four types of hypersensitivity reactions?

A

Type I (Immediate, IgE-mediated) – Allergies, anaphylaxis.

Type II (Cytotoxic, IgG/IgM) – Hemolytic anemia, Graves’ disease.

Type III (Immune Complex) – Lupus, serum sickness.

Type IV (Delayed, T-cell mediated) – Contact dermatitis, TB test​

20
Q

What is the mechanism of Type I hypersensitivity?

A

Allergen → IgE binds mast cells → Histamine release → Inflammation (e.g., asthma, anaphylaxis)​

21
Q

What is an autoimmune disease?

A

A disorder where the immune system attacks self-antigens, leading to chronic inflammation

22
Q

Give examples of common autoimmune diseases.

A
  • Systemic lupus erythematosus (SLE) – Multi-organ involvement.
  • Rheumatoid arthritis (RA) – Chronic joint inflammation.
  • Type 1 diabetes – Autoimmune destruction of pancreatic β-cells.
  • Multiple sclerosis (MS) – CNS myelin destruction
23
Q

What is the major risk in organ transplantation?

A

Graft rejection due to immune response against non-self antigens

24
Q

What are the three types of transplant rejection?

A

1) Hyperacute rejection (minutes-hours): Pre-formed antibodies against donor tissue.

2) Acute rejection (days-weeks): T-cell mediated immune response.

3) Chronic rejection (months-years): Fibrosis and gradual organ dysfunction

25
How can transplant rejection be prevented?
Immunosuppressive therapy (e.g., cyclosporine, corticosteroids, tacrolimus)​