- TTP = Thrombotic Microangiopathy (TMA)
- Core features:
- MAHA
- Thrombocytopenia
Types of TMA
- TTP
- ADAMTS13 deficiency
- Cleaves vWF multimers
- Deficiency → large vWF multimers → platelet trapping
- Acquired
- 95%
- Autoantibody
- Hereditary
- 5%
- HUS
- Typical
- childhood
- Shiga / Shiga-like toxin
- Atypical
- Adult
- Complement-mediated
- Drug-induced TMA
Pathophysiology
- Microthrombi in arterioles & capillaries
- Platelet consumption → thrombocytopenia
- RBC fragmentation → MAHA
Clinical Features
- Bleeding
- Anemia symptoms
- Neurological:
- Headache
- Confusion
- Young stroke
- Renal involvement
- Absent
Laboratory Findings
- Platelets ↓
- Hemoglobin ↓
- Haptoglobin ↓
- LDH ↑
- Coombs – Negative
- Peripheral smear
- Schistocytes
- RFT / LFT
- Normal
HUS vs TTP
Feature | HUS | TTP |
Major organ | Kidney | Brain |
Renal failure | Present | Absent |
Management
- Plasma exchange (PLEX) + Rituximab – TOC
TTP Mimics
- Malignant hypertension
- Antiphospholipid antibody syndrome
- Sepsis
- Pre-eclampsia
- Scleroderma renal crisis
Drug-induced TMA
- Mitomycin
- Cisplatin
- Gemcitabine
- Calcineurin inhibitors
- Ticlopidine
- Clopidogrel