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. 2022 Jan 31;12(2):220. doi: 10.3390/life12020220

Table 6.

Pathogenetic features of combined micro-macrothrombosis in arterial and venous systems per “two-path unifying theory” of hemostasis.

Clinical Phenotype Arterial Combined Micro-Macrothrombosis Venous Combined Micro-Macrothrombosis
Pathologic nature of thrombosis
(Examples) Gangrene: Venous circulatory congestion syndrome:
SPG, limb gangrene, Fournier’s disease,
PF, diabetic gangrene, necrotizing fasciitis
Proximal/central DVT, VTE, PTE, CVST, PVT, IVCT/SVCT, SVT, Budd-Chiari syndrome
Primary event
Vascular injury (ECs) Diseases causing microvascular endotheliopathy
(e.g., sepsis, diabetes, pregnancy)
Diseases causing venous endotheliopathy
(e.g., sepsis, diabetes, pregnancy, autoimmunity)
Vascular pathology site Disseminated aEA-VMTD at terminal arterial tree Regional vEA-VMTD at vascular injury site
Activated hemostatic path ULVWF path ULVWF path
Thrombosis component Microthrombi strings Microthrombi strings
Secondary event
Vascular injury (SET) Arterial vascular damage
(e.g., surgery, vascular accesses/devices)
Venous vascular damage
(e.g., surgery, vascular accesses/devices)
Pathology Fibrin clots in arterial system Fibrin clots in venous system
Vascular pathology site Terminal arterial vasculature tree Large vein or pulmonary artery
Activated hemostatic path TF path TF path
Thrombosis component Fibrin meshes Fibrin meshes
Pathogenesis
Mechanism Unifying of microthrombi string and fibrin meshes in arterial system as minute macrothrombi Unifying of microthrombi strings and fibrin meshes in venous system often as connected macrothrombi
Thrombosis character Microthrombi strings-fibrin meshes complex Microthrombi strings-fibrin meshes complex
Thrombosis form and effect Multiple terminal efferent digit anoxia and peripheral gangrene Connected and regional, with circulatory afferent flow with venous circulatory congestion syndrome

Note: aEA-VMTD, arterial endotheliopathy-associated vascular microthrombotic disease; vEA-VMTD, venous-VMTD; CVST, cerebral venous sinus thrombosis; ECs, endothelial cells, DVT, deep venous thrombosis; IVCT, inferior vena cava thrombosis; PF, purpura fulminans; PVT, portal vein thrombosis; SET, subendothelial issue; SPG, symmetrical peripheral gangrene; SVCT, superior vena cava thrombosis; SVT, splanchnic vein thrombosis; TF, tissue factor; PTE, pulmonary thromboembolism; ULVWF, ultra large von Willebrand factor: VTE, venous thromboembolism.