Display options
Cite
Sampagar AA, Jahagirdar RR, Bafna VS, et al. Juvenile granulosa cell tumor associated with Ollier disease. Indian J Med Paediatr Oncol. 2016;37(4):293-295doi: 10.4103/0971-5851.195749.
Sampagar, A. A., Jahagirdar, R. R., Bafna, V. S., & Bartakke, S. P. (2016). Juvenile granulosa cell tumor associated with Ollier disease. Indian journal of medical and paediatric oncology : official journal of Indian Society of Medical & Paediatric Oncology, 37(4), 293-295. https://doi.org/10.4103/0971-5851.195749
Sampagar, Abhilasha Ashok, et al. "Juvenile granulosa cell tumor associated with Ollier disease." Indian journal of medical and paediatric oncology : official journal of Indian Society of Medical & Paediatric Oncology vol. 37,4 (2016): 293-295. doi: https://doi.org/10.4103/0971-5851.195749
Sampagar AA, Jahagirdar RR, Bafna VS, Bartakke SP. Juvenile granulosa cell tumor associated with Ollier disease. Indian J Med Paediatr Oncol. 2016 Oct-Dec;37(4):293-295. doi: 10.4103/0971-5851.195749. PMID: 28144098; PMCID: PMC5234168.
Copy Download .nbib Format: NLM
Share it on

Indian J Med Paediatr Oncol. 2016 Oct-Dec;37(4):293-295. doi: 10.4103/0971-5851.195749.

Juvenile granulosa cell tumor associated with Ollier disease.

Indian journal of medical and paediatric oncology : official journal of Indian Society of Medical & Paediatric Oncology

Abhilasha Ashok Sampagar, Rahul R Jahagirdar, Vibha Sanjay Bafna, Sandip P Bartakke

Affiliations

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

PMID: 28144098 PMCID: PMC5234168 DOI: 10.4103/0971-5851.195749

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; Maffucci syndrome; Ollier disease; juvenile granulosa cell tumor

Conflict of interest statement

There are no conflicts of interest.

References

  1. Orphanet J Rare Dis. 2006 Sep 22;1:37 - PubMed
  2. Indian J Surg Oncol. 2013 Mar;4(1):37-47 - PubMed
  3. J Orthop Sci. 2006 Jul;11(4):412-23 - PubMed
  4. Clin Radiol. 2005 Dec;60(12 ):1306-10 - PubMed
  5. Chin Med J (Engl). 2004 Oct;117(10):1592-4 - PubMed
  6. Radiographics. 2014 Nov-Dec;34(7):2039-55 - PubMed
  7. Singapore Med J. 2008 Oct;49(10 ):841-5; quiz 846 - PubMed
  8. Cancer. 1984 Apr 1;53(7):1605-8 - PubMed
  9. J Pediatr Orthop B. 2003 Mar;12 (2):147-50 - PubMed

Publication Types