Relapsing polychondritis (RP) is a rare, autoimmune, multisystemic disease with unknown etiology. It affects all types of cartilages and proteoglycan-rich structures. 1 The prominent manifestations of the disease are recurrent inflammatory involvements of eye, otorhinolaryngeal and bronchial cartilage, cardiovascular system, musculoskeletal structures, kidney, central nervous system and skin. 2 The most frequent presenting feature of the disease is auricular chondritis. 1