Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 759-761 |
| Number of pages | 3 |
| Journal | Journal of Craniofacial Surgery |
| Volume | 13 |
| Issue number | 6 |
| Publication status | Published - Nov 2002 |
Keywords
- Eosinophilic granuloma
- Hand-Schüller-Christian
- X-cell histiocytosis
ASJC Scopus subject areas
- Surgery
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Cite this
Becelli, R., Carboni, A., Gianni, C., Alterio, A., & Renzi, G. (2002). A rare condition of Hand-Schüller-Christian disease. Journal of Craniofacial Surgery, 13(6), 759-761.