Objective: Erdheim-Chester disease is a rare form of non-Langerhans cell histiocytosis unknown etiology. It multisystemic that can involve bones, skin, brain, retroperitoneum, cardiovascular system, endocrine and lungs. Diagnosis made by clinical findings, imaging results, histopathological examination. BRAFV600E (B-rapidly accelerated fibrosarcoma gene) mutation found in more than half the cas...