The authors present the clinical case of a 61-year-old patient with Hand-Schüller-Christian disease associated with multisystemic involvement. The onset of such puzzling symptoms and the extremely rarity of this disease in a patient of such advanced age resulted in a delayed diagnosis and subsequently delayed treatment of the patient.
|Number of pages||3|
|Journal||Journal of Craniofacial Surgery|
|Publication status||Published - Nov 2002|
- Eosinophilic granuloma
- X-cell histiocytosis
ASJC Scopus subject areas