Which of the following histiocytosis clinical syndromes accounts for 15% to 40% of these cases, occurs in children between 1 and 5 years of age, and typically displays multiple geographic osteolytic lesions in the skull, pelvis, and long bones?

Question

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Hand-Schüller-Christian disease is a type of Langerhans cell histiocytosis that occurs in children aged 1 to 5 years and is characterized by multiple osteolytic lesions, often in the skull, pelvis, and long bones.

Which of the Following Histiocytosis Clinical Syndromes Accounts for 15