Aneurysmal bone cyst (ABC) was described for the first time by Jaffe and Lichtenstein in 1942 as a particular variant of solitary unicameral bone cyst [1]. It is currently defined by the World Health Organization's histologic classification of bone tumors as "expansive and osteolytic benign bone tumor consisting of bloodfilled cavities lined by connective tissue septa" [2]. ABC is very rare representing only 1-2% of all bone tumors and 5-6% of benign bone tumors [3]. This tumor can occur at any age but remains particularly frequent in children and adolescents with a maximum incidence before the age of 20 years [3,4]. Likewise, all bones can be affected by this tumor; the long bones are the most frequently involved [3,4]. Classically this bone pseudotumor is unique [2][3][4] but can exceptionally be multiple [5], recurrent [6], or with distant metatstases [7] posing a real diagnostic challenge for clinicians [5][6][7]. From the so-called "atypical" or "unusual" variants of ABC, multifocal presentation is exceptional with only few sporadic cases