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Copyright ©The Author(s) 2024.
World J Transplant. Mar 18, 2024; 14(1): 90277
Published online Mar 18, 2024. doi: 10.5500/wjt.v14.i1.90277
Table 1 Etiology and classification of thrombotic microangiopathies
Primary TMAs
Shiga toxin-producing E. Coli-associated HUS
Thrombotic thrombocytopenic purpura
Atypical HUS or complement-mediated
Secondary TMAs
Infections including viral, fungal, and bacterial
Drugs including immunosuppressants and chemotherapeutic agents
Autoimmune diseases
Malignant hypertension
Malignancy
Metabolic defects
Pregnancy
Transplantation, both hematopoietic stem cell transplantation and solid organ transplantation
Disseminated intravascular coagulation
Radiation
Table 2 Etiology of post-transplant thrombotic microangiopathies
Recurrent TMA, rare (5%-10% of cases)
    Mutations in complement regulatory factor genes [e.g., factor H, factor I, membrane cofactor protein, etc.]
    Mutations in complement genes (e.g., C3)
    TMA associated with autoantibodies (anti-factor H antibodies, anti-ADAMTS13 antibodies, antiphospholipid antibodies)
    TMA associated with autoimmune diseases (scleroderma and systemic lupus erythematosus)
De-novo TMA, common (90%-95% of cases)
    Associated with the type of donor and organ procurement procedure, e.g. Ischemia reperfusion injury
    Drugs
        I: Calcineurin inhibitors-associated TMA
        II: Mammalian target of rapamycin inhibitors-associated TMA
    Antibody-mediated rejection associated TMA
    Infection-associated TMA
        I: Viral, e.g. hepatitis C virus, parvovirus B19, and cytomegalovirus)
        II: Fungal
        III: Bacterial
    Other rare causes, such as malignancy, other drugs, and pregnancy
Table 3 Morphological features of thrombotic microangiopathies
Active lesions
1 Glomerular lesions (Light microscopy):
Intraluminal thrombi
Endothelial swelling or denudation
Endothelial swelling or denudation
Subendothelial space widening (bloodless glomeruli)
Mesangiolysis
Microaneurysms
2 Arteriolar lesions:
Intraluminal thrombi
Endothelial swelling or denudation
Intramural fibrin
Fragmented red blood cells
3 Arterial lesions:
Intraluminal thrombi
Intimal edema
Myxoid intimal swelling
Myocyte necrosis
Intramural fibrin
Fragmentation of red blood cells
Chronic lesions
1 Glomerular lesions (Light microscopy):
Double contours of peripheral capillary walls, with variable mesangial interposition
2 Arteriolar lesions:
Hyaline deposits
3 Arterial lesions:
Fibrous intimal thickening with concentric lamination (onion-skining)