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RARE CASE MEDULLOBLASTOMA WITH MANDIBULAR SECONDARY

SMRITI GAUR GAUR GAUR GAUR

Abstract


Aim to report a rare case of medulloblastoma with mandibular secondaries.Background Medulloblastoma is an embryonal tumor, common in children. It has a high malignant potential with a propensity to spread to lymphatic organs and bone, mostly vertebrae, but mandible involvement is very rare. Case History A 10 year old male child was diagnosed with cerebellar medulloblastoma , with spinal involvement at D5 vertebral level, in 2010, for which he was treated with near total excision followed by CSI 36 Gy, with posterior fossa boost up to 54 Gy. He received 6 cycles of cisplatin and            etoposide, after which there was complete remission. After being disease free on subsequent follow up, he reported again with a swelling of the jaw in 2013, which was proved to be as secondaries from medulloblastoma. He was treated with radiotherapy to a dose of 46 Gy to the mandibular   swelling. There was a partial response in the lesion. The  patient was put on salvage chemotherapy then using   vincristine and cyclophosphamide.Conclusion                               Medulloblastoma metastasizing to the mandible is a rare event. Radiotherapy to the osseous secondary was not found to completely resolve it. However, with the use of second line chemotherapy, more successful treatment might be possible but the outcome is generally poor.

 


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References


Chapter in book: Freeman CR, Farmer JP, Taylor RE. Central Nervous System Tumors In Children.In: Halperin EC, WAzer DE, Perez CA, Brady LW editors. Perez and Brady’s Principles and Practice Of Radiation Oncology. 6th ed.Lippincott Williams & Wilkins, 2013;p1647-1651.

Rochkind S, Blatt I, Sadeh M, Goldhammer Y. Extracranial metastases of medulloblastoma in adults: literature review . Journal of Neurology, Neurosurgery, and Psychiatry 1991;54:80-86

Srinivas C, Gupta T, Rajasekharan P, Munshi A. Bilateral

mandibular metastases in medulloblastoma. Journal of Clinical Neuroscience 2009;16:325-327

Barai S Bandopadhayaya G P, Julka P K, Dhanapathi H, Haloi A K, Seith A. Cerebellar medulloblastoma presenting with skeletal metastasis. J Postgrad Med 2004;50:110-2

Brisson C, Lelong-Rebel I, Mottolese C, Jouvet A, Fevre-Montange M, Saint Pierre G, et al. Establishment of human tumoral ependymal cell lines and coculture with tubular-like human endothelial cells. Int J Oncol 2002;21:775-85

Chapter in a book:Mehta M, Vogelbaum MA, Chang S, Patel N.Neoplasms Of The Central. Nervous System.In: DeVita, Vincent T, Lawrence, Theodore S, Rosenberg, Steven A editors. Devita, Hellman & Rosenberg's Cancer Principles & Practice of Oncology. 9th ed. Lippincott Williams & Wilkins,2011;p.1730-1733.

Gajjar A, Hernan R, Kocak M, Fuller C, Lee Y, McKinnon PJ et al.Clinical, Histopathologic, and Molecular Markers of Prognosis: Toward a New Disease Risk Stratification System for Medulloblastoma. JCO 2004;22: 6 984-993

Biologic Risk Stratification of Medulloblastoma:The Real Time Is Now.FisherPG,Burger PC, Eberhart CG.

JCO 2004; 22: 6 971-974 Cho YJ, Tsherniak A, Tamayo P, Santagata S, Ligon A, Greulich H et al.Integrative Genomic Analysis of Medulloblastoma Identifies a Molecular Subgroup That Drives Poor Clinical Outcome.

JCO 2011;29:1424-1430 Panosyan EH, Ikeda KA, ChangVY, Laks DR, Reeb CL, Bowles LV et al. High-Dose

Chemotherapy with Autologous Hematopoietic Stem-Cell Rescue for Pediatric Brain Tumor Patients: A Single Institution Experience from UCLA. Journal of Transplantation 2011;2011:


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