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Indian Journal of Medical and Paediatric Oncology
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Year : 2016  |  Volume : 37  |  Issue : 4  |  Page : 293-295

Juvenile granulosa cell tumor associated with Ollier disease

Department of Pediatrics, Division of Pediatric Oncology, Bharati Vidyapeeth Medical College and Hospital, Pune, Maharashtra, India

Correspondence Address:
Abhilasha Ashok Sampagar
Department of Pediatrics, Bharati Hospital, 3rd Floor, Katraj, Dhanakwadi, Pune, Maharashtra
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0971-5851.195749

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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.

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