CC BY-NC-ND 4.0 · Asian J Neurosurg 2021; 16(02): 398-401
DOI: 10.4103/ajns.AJNS_439_20
Case Report

Recurrent papillary tumor of pineal region misdiagnosed as pineocytoma 9-years ago

Nirav Mehta
Department of Neurosurgery, Bombay Hospital Institute of Medical Sciences, Mumbai, Maharashtra
,
Gaurav Gupta
Department of Neurosurgery, Bombay Hospital Institute of Medical Sciences, Mumbai, Maharashtra
,
Salman Shaikh
Department of Neurosurgery, Bombay Hospital Institute of Medical Sciences, Mumbai, Maharashtra
› Author Affiliations

Primary tumors of the pineal gland occur infrequently with a preponderance of either parenchymal tumors or germ cells tumors. Papillary tumor of the pineal region is a rare neuroepithelial lesion that arises exclusively in the pineal region. They have been designated as either Grade II or Grade III lesions as per the 2016 WHO classification of central nervous system tumors. Clinically, they usually present with obstructive hydrocephalus and visual disturbance. On imaging, these tumors are solid-cystic, heterogeneously enhancing, and show T2 hyperintensity. Pathologically, they can closely resemble a Grade I pineocytoma and immunohistochemistry is essential to differentiate the two. No definite guidelines exist to confirm the ideal protocol of treatment. Evidence regarding the role of radiation after surgery is limited to case reports and series. Adjuvant therapy is usually recommended for tumors with subtotal excision, high proliferative/mitotic index, or proven metastasis. We describe a case of a 29-year-old male with a recurrent papillary tumor of the pineal region, 9 years after primary surgery where it was misdiagnosed as a pineocytoma. The tumor was effectively controlled with surgical excision, cerebrospinal fluid diversion, and adjuvant radiation for 8 years before showing two recurrences within a span of 6 months with a rising proliferation index.

Financial support and sponsorship

Nil.




Publication History

Received: 17 September 2020

Accepted: 13 March 2021

Article published online:
16 August 2022

© 2021. Asian Congress of Neurological Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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  • References

  • 1 Villano JL, Propp JM, Porter KR, Stewart AK, Valyi-Nagy T, Li X, et al. Malignant pineal germ-cell tumors: An analysis of cases from three tumor registries. Neuro Oncol 2008;10:121-30.
  • 2 Trojanowski JQ, Tascos NA, Rorke LB. Malignant pineocytoma with prominent papillary features. Cancer 1982;50:1789-93.
  • 3 Fèvre-Montange M, Hasselblatt M, Figarella-Branger D, Chauveinc L, Champier J, Saint-Pierre G, et al. Prognosis and histopathologic features in papillary tumors of the pineal region: A retrospective multicenter study of 31 cases. J Neuropathol Exp Neurol 2006;65:1004-11.
  • 4 Louis DN, Perry A, Reifenberger G, von Deimling A, Figarella-Branger D, Cavenee WK, et al. The 2016 World Health Organization Classification of Tumors of the Central Nervous System: A summary. Acta Neuropathol 2016;131:803-20.
  • 5 Jouvet A, Fauchon F, Liberski P, Saint-Pierre G, Didier-Bazes M, Heitzmann A, et al. Papillary tumor of the pineal region. Am J Surg Pathol 2003;27:505-12.
  • 6 Verma A, Epari S, Bakiratharajan D, Sahay A, Goel N, Chinnaswamy G, et al. Primary pineal tumors – Unraveling histological challenges and certain clinical myths. Neurol India 2019;67:491-502.
  • 7 Heim S, Beschorner R, Mittelbronn M, Keyvani K, Riemenschneider MJ, Vajtai I, et al. Increased mitotic and proliferative activity are associated with worse prognosis in papillary tumors of the pineal region. Am J Surg Pathol 2014;38:106-10.
  • 8 Chatterjee D, Gupta K, Kumar N, Chhabra R, Radotra BD. Papillary tumor of the pineal region-report of three cases with literature review. Neurol India 2015;63:567-70.
  • 9 Chang AH, Fuller GN, Debnam JM, Karis JP, Coons SW, Ross JS, et al. MR imaging of papillary tumor of the pineal region. AJNR Am J Neuroradiol 2008;29:187-9.
  • 10 Patel SK, Tomei KL, Christiano LD, Baisre A, Liu JK. Complete regression of papillary tumor of the pineal region after radiation therapy: Case report and review of the literature. J Neurooncol 2012;107:427-34.
  • 11 Cardenas R, Javalkar V, Haydel J, Wadhwa R, Fowler M, Scheithauer B, et al. Papillary tumor of pineal region: Prolonged control rate after gamma knife radiosurgery – A case report and review of literature. Neurol India 2010;58:471-6.
  • 12 Fauchon F, Hasselblatt M, Jouvet A, Champier J, Popovic M, Kirollos R, et al. Role of surgery, radiotherapy and chemotherapy in papillary tumors of the pineal region: A multicenter study. J Neurooncol 2013;112:223-31.
  • 13 Edson MA, Fuller GN, Allen PK, Levine NB, Ghia AJ, Mahajan A, et al. Outcomes after surgery and radiotherapy for papillary tumor of the pineal region. World Neurosurg 2015;84:76-81.
  • 14 Cohen AL, Salzman K, Palmer C, Jensen R, Colman H. Bevacizumab is effective for recurrent papillary tumor of the pineal region: First report. Case Rep Oncol 2013;6:434-40.