Abstract
Juvenile granulosa cell tumor (JGCT) is a rare neoplasm of childhood. Interestingly,
it is known to be associated with Ollier disease, which is a rare bone disease characterized
by multiple enchondromatosis. There is paucity of literature about the co-occurence
of these two conditions. However, this association is noteworthy because these two
conditions share a common pathogenesis. We report a case of JGCT in a 2.5-year-old
female child in which multiple enchondromas mimicking bony metastasis were an incidental
finding during routine workup for tumor staging, thus leading to a diagnosis of Ollier
disease.
Keywords
Enchondroma - juvenile granulosa cell tumor - Maffucci syndrome - Ollier disease
