ITP , TTP vs. HUS vs. DIC Flashcards

(21 cards)

1
Q

Autoantibodies against GPIIb/IIIa receptors

A

Immune Thrombocytopenia (ITP)

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2
Q

Secondary (Associated Conditions) of immune thrombocytopenia

A

o Autoimmune: Lupus (SLE)
o Hematologic: CLL
o Infectious: HIV, Hepatitis C, CMV, Varicella

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3
Q

Treatment of Immune thrombocytopenia
In children:

A

Often self-resolving, monitor unless severe

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4
Q

Treatment of Immune thrombocytopenia
Adult : Often chronic, requires treatment if platelets <30,000/µL

A

o First-line: Corticosteroids
o Second-line: IVIG
o Refractory cases: Splenectomy
o Platelet transfusion only for severe bleeding

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5
Q

Deficiency of ADAMTS13 (vWF-cleaving protease)

A

Thrombotic Thrombocytopenic Purpura
(TTP)

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6
Q

Accumulation of large vWF multimers → platelet aggregation

A

Thrombotic Thrombocytopenic Purpura
(TTP)

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7
Q

Clinical Features (Pentad) of TTP

A
  1. Thrombocytopenia (petechiae, purpura)
  2. Microangiopathic Hemolytic Anemia (MAHA) (schistocytes, ↑ LDH, ↓
    haptoglobin)
  3. Neurologic symptoms (confusion, seizures, stroke)
  4. Fever
  5. Renal dysfunction (mild)
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8
Q

Diagnosis of TTP

A

 CBC + Peripheral Smear: Schistocytes
 ADAMTS13 Activity: Severe deficiency (<10%) (Not required before starting
treatment)
 Normal PT/PTT (Unlike DIC)

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9
Q

Treatment of TTI

A

 Plasma Exchange (PEX) → Lifesaving
 Glucocorticoids
 Platelet transfusion is contraindicated (worsens thrombosis)

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10
Q

Platelet-rich thrombi in small vessels

A

TTP

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11
Q

Platelet-rich thrombi in renal vasculature

A

Hemolytic Uremic Syndrome (HUS)

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12
Q

Shiga-like toxin from E. coli O157:H7 → endothelial damage

A

HUS

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13
Q

Clinical Features (Triad) of HUS

A
  1. Thrombocytopenia
  2. MAHA (schistocytes)
  3. Acute kidney injury (↑ creatinine)
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14
Q

Diagnosis of HUS

A

 CBC + Peripheral Smear: Schistocytes
 Kidney Function: ↑ Creatinine, ↑ BUN
 Stool culture for E. coli O157:H7

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15
Q

Treatment of HUS

A

 Supportive care (fluids, dialysis if needed)
 No plasma exchange (unlike TTP)

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16
Q

Uncontrolled clotting activation → microthrombi + bleeding

17
Q

Consumption of platelets & coagulation factors

18
Q

Common Causes Of DIC

A

 Sepsis (bacterial endotoxins)
 Obstetric emergencies (amniotic fluid embolism)
 Malignancy (APL, adenocarcinomas)

19
Q

Clinical Features of DIC

A

 Thrombocytopenia + MAHA (schistocytes)
 Diffuse bleeding (IV sites, mucosa)
 Organ dysfunction (kidney failure, ARDS)

20
Q

Diagnosis of DIC

A

 ↑ PT, ↑ PTT, ↑ INR
 ↑ D-dimer (fibrin degradation product)
 ↓ Fibrinogen
 Peripheral smear: Schistocytes

21
Q

Treatment of DIC

A

 Treat underlying cause
 Supportive care (blood, platelet transfusions)
 Fresh frozen plasma (clotting factor replacement)