Angioedema is a characterized by localized non-pitting swelling of the deeper layers of the skin. Lips, eyelids, and genitalia are sites of predilection. Clinically, angioedema can be asymptomatic or more often be accompanied by a pruritic sensation. Co-existence of angioedema and urticaria has been extensively described. 1 Moreover, isolated angioedema accompanied by sharp pain or a stinging sensation, without additional cutaneous involvement, has been previously reported. 2 Angioedema might be accompanied by additional symptoms such as abdominal cramps, nausea, and vomiting. Life threating, bronchospasm, and anaphylaxis can occur in severe cases. 3 Isolated angioedema may be inherited or acquired. 4 Inherited angioedema usually represents quantitative or functional deficiencies of C1 esterase inhibitor. Since measurements of C4 levels are usually decreased between attacks, they might be helpful for screening purposes. 4 A rare form of hereditary angioedema (type III), in which C1 esterase inhibitor levels are normal, is suggested to be partially due to Factor XII (FXII) deficiency. Genetic screening for FXII mutations should be considered in patients with angioedema of uncertain etiopathogenesis. 5 Acquired isolated angioedema is a heterogeneous group of diseases, resulting from various etiological factors via a histaminergic mechanism including drugs (such as