Langerhans cell histiocytosis (LCH) is a rare hematological disease, more common in pediatric populations. A 26-year-old man with biopsy-proven cutaneous LCH underwent F-18-FDG PET/CT systemic staging. F-18-FDG PET/CT highlighted multiple sites of avid cutaneous disease within the natal cleft. Additional characteristic cystic lung disease was seen on the CT component and focal uptake in the pituitary stalk/hypothalamic region noted, a common but occult site of disease in this patient. Because of the rarity of adult-onset cutaneous LCH, guidance on management and staging is lacking. 18F-FDG PET/CT is critical to baseline evaluation of systemic disease, as illustrated here.
机构:
UNIV LONDON ST BARTHOLOMEWS HOSP MED COLL,DEPT HISTOPATHOL,LONDON EC1A 7BE,ENGLANDUNIV LONDON ST BARTHOLOMEWS HOSP MED COLL,DEPT HISTOPATHOL,LONDON EC1A 7BE,ENGLAND
Malpas, JS
Norton, AJ
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机构:
UNIV LONDON ST BARTHOLOMEWS HOSP MED COLL,DEPT HISTOPATHOL,LONDON EC1A 7BE,ENGLANDUNIV LONDON ST BARTHOLOMEWS HOSP MED COLL,DEPT HISTOPATHOL,LONDON EC1A 7BE,ENGLAND
Norton, AJ
MEDICAL AND PEDIATRIC ONCOLOGY,
1996,
27
(06):
: 540
-
546