Version June 2024
| Common | |
| Venous | |
| Arterial | |
| Neuropathic | |
| Uncommon | |
| Physical | Thermal burns, cold injury, radiation, trauma, factitial |
| Bites | Spider |
| Infection | Bacterial, fungal, spirochete, protozoal |
| Vasculopathies | Livedoid vasculopathy, Buerger's disease |
| Hypercoagulable states (inherited and acquired) | Factor V Leiden, antiphospholipid antibody syndrome, protein C and S deficiency, anti-thrombin III deficiency, prothrombin G20210A mutation, hyperhomocysteinemia and methylenetetrahydrofolate reductase (MTHFR) polymorphism |
| Vaso-occlusive disorders | Calciphylaxis, cholesterol emboli, type I cryoglobulinemia, cryofibrinogenemia, oxalosis |
| Vasculitis (small and medium-sized vessel) | Henoch-Schönlein purpura, rheumatoid vasculitis, mixed cryoglobulinemia, polyarteritis nodosa, granulomatosis with polyangiitis, lupus erythematosus |
| Pyoderma gangrenosum | |
| Necrobiosis lipoidica | |
| Panniculitis | Alpha-1-antitrypsin deficiency, pancreatic fat necrosis, erythema induratum (nodular vasculitis) |
| Neoplastic conditions | Squamous cell carcinoma, basal cell carcinoma, cutaneous T and B cell lymphoma, Kaposi's sarcoma |
| Systemic sclerosis | |
| Hematologic disease | Hemoglobinopathies, thrombocytosis |
| Drugs | Hydroxyurea, warfarin, heparin |
| Metabolic | Calcinosis cutis, gout, prolidase deficiency, leukocyte adhesion deficiency, Werner syndrome |
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