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Table 2 Differential diagnosis of necrotic skin lesions in an infanta

From: Empiric treatment of protracted idiopathic purpura fulminans in an infant: a case report and review of the literature

System

Diagnoses

Hematologic

Idiopathic thrombocytopenic purpura

Thrombotic thrombocytopenic purpura

Coagulation factor deficiency

Platelet function disorder

Thromboembolic disease

Lupus/anti-phospholipid antibodies

Cryoglobulinemia

Porphyria

Idiopathic red blood cell agglutination

Idiopathic PF

Neonatal PF or other thrombophilic mutation

Infectious

Cellulitis with or without atypical organisms or fungi

Endocarditis (bacterial, fungal or marantic)

Inflammatory

Panniculitis secondary to α1-anti-trypsin deficiency

Pemphigus vulgaris

Pyoderma gangrenosum

Epidermolysis

Vascular

HSP

Leukocytoclastic vasculitis

Hematoma with compartment syndrome

Neoplastic

Leukemia

Lymphoma

Essential thrombocythemia

Cutaneous T-cell lymphoma

Nutritional

Vitamin deficiency (vitamin K)

Mineral deficiency (zinc)

Environmental

Toxic exposure (for example, heavy metals)

Congenital

Combined immune deficiency

Prolidase deficiency

Leukocyte adhesion deficiency

Chronic granulomatous disease

γ-globulinemia

Spinal muscular atrophy

Trauma

 
  1. aPF, purpura fulminans; HSP, Henoch-Schonlein purpura.