Odell W D, Doggett R S
Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City 84132.
J Clin Endocrinol Metab. 1993 Mar;76(3):777-80. doi: 10.1210/jcem.76.3.8445037.
A 33-yr-old male developed typical symptoms and findings of diabetes insipidus. A computed tomographic scan of the hypothalamus/pituitary was normal, and he was diagnosed as having idiopathic diabetes insipidus. At age 38 yr, he developed two 1- to 2-mm reddish papules on his skin. Biopsy revealed infiltrative histiocytes laden with lipid. Bone scans and bone x-rays showed widespread osteolytic and osteoblastic disease. The disease was diagnosed as a rare disseminated histiocytic disorder, xanthoma disseminatum. A classification of histiocytic disease is presented.