“…The syndromes of purpura fulminans, thrombotic thrombocytopenic purpura (thrombotic microangiopathic haemolytic anaemia or Moschcowitz's syndrome), periarteritis nodosa and anaphylactoid purpura (Henoch-Schonlein purpura) all have an obscure aetiology and pathogenesis. Many authors (Crawford and Riddler, 1959;Heal and Kent, 1953;Chambers et al, 1952;Turin et al, 1959;Seinfeld et al, 1960;Balf, 1951;Kingsley and Aquino, 1958;Craig and Gitlin, 1957;Wile and Sturgeon, 1956;Gairdner, 1948;Robinson, Orchard and Eden, 1958;Vernier, Worthen, Peterson, Colle and Good, 1961) feel that the primary fault appears to be a focal vascular lesion with swelling of the endothelium, rupture of the vessel wall and haemorrhage. These authorities have suggested independently that each disease is primarily a vascular disorder caused by an abnormal immunological mechanism of unknown origin.…”