“…This is probably because, the most papers on the subject being written different languages in the world and AHEI is called Henoch-Schönlein purpura in the United States. Although most of the prints were in case reports (Babic et al, 2008;Can et al, 2006;Di Lernia et al, 2004;Garty et al, 2002;Michael, 2006;Millard et al, 1999;Macea et al, 2003;Obeid et al, 2008;Serna et al, 1994, Silveira & Braganca, 2006, case series were also published (Alp et al, 2009;Caksen et al, 2002;Fiore et al, 2008;Gelmetti et al, 1985;Gonggryp & Todd, 1998;Ince et al, 1995;Karremann et al, 2009;Krause et al, 1996;Legrain et al, 1991;Poyrazoglu et al, 2003;Saraclar et al, 1990;Sites et al, 2008). Today, AHEI is considered as a separate entity, but not a variant of Henoch-Schönlein purpura, with clinical findings and prognosis.…”