2 weeks, both in percentage change and in absolute value of the change.Ixekizumab induced immediate improvement in inflammatory markers in patients with GPP with systemic inflammation. This indicates that ixekizumab is a good treatment option for patients in the acute phase or in a flare of GPP, and that its effectiveness can be expected after a few days. Although BT seemed to decrease 1 day after initiation of ixekizumab, no significant difference was observed. The use of antipyretics may have affected the results. GMA is an extracorporeal circulation therapy that removes activated granulocytes and monocytes. It can be easily introduced in clinics and hospitals where haemodialysis is performed. Its safety profile 5 allows for its administration without screening and for its concomitant use with other therapies. GMA is usually not used as monotherapy but, rather, as adjuvant or neoadjuvant therapy for GPP. We previously reported that GMA induced a significant decrease in BT but not in WBC count or CRP after 2 days, 6 suggesting that GMA could be a good adjuvant therapy with ixekizumab. The main limitation of this study is that ixekizumab was not used as monotherapy.