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INVITED COMMENTARY
Year : 2021  |  Volume : 16  |  Issue : 3  |  Page : 655

Pineal tumors: A pathological challenge


Department of Neurosurgery, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences; Brain and Spinal Cord Injury Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran

Date of Submission12-Mar-2021
Date of Decision25-May-2021
Date of Acceptance30-May-2021
Date of Web Publication14-Sep-2021

Correspondence Address:
Dr. Seyed Amir Hossein Javadi
Keshavarz Blvd, Imam Khomeini Hospital Complex, 14197, Tehran
Iran
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ajns.AJNS_106_21

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How to cite this article:
Javadi SA. Pineal tumors: A pathological challenge. Asian J Neurosurg 2021;16:655

How to cite this URL:
Javadi SA. Pineal tumors: A pathological challenge. Asian J Neurosurg [serial online] 2021 [cited 2021 Dec 1];16:655. Available from: https://www.asianjns.org/text.asp?2021/16/3/655/324443

It is an honor for having been invited to write a commentary to the published paper titled, “Recurrent Papillary Tumour of Pineal Region Misdiagnosed as Pineocytoma 9 Years Ago: A Case Report.” The current paper explains the pathological challenge of pineal tumors which would affect treatment as well. Pathological classification of brain tumors has evolved during the last decades. Introduction of bio-molecular markers and new modalities made significant differentiations in pathologies that modified their treatment and prognosis.

Pineal tumors are challenging type of brain lesions according to their anatomy, surgical approaches, and pathologic subtypes. Considering pathology, the most common tumors are pineal parenchymal tumors and germ cell tumors.[1] Pineal parenchymal tumors are divided into pineocytoma, pineal parenchymal tumor with intermediate differentiation, and pineoblastoma. Precise differential diagnosis is critical for treatment planning.

Papillary tumor of the pineal region (PTPR) is a rare neuro-epithelial tumor categorized as Grade II or Grade III lesions and resembles a Grade I pineocytoma. Therefore, immunohistochemistry is essential to differentiate them. Unlike germ cell tumors of pineal region, surgery seems to be the optimal primary treatment for PTPR to achieve cytoreduction followed by adjuvant therapies. The current paper emphasizes the role of pathological diagnosis in a multidisciplinary management of brain tumors. Surgical approach to intracranial lesions carries a high risk of various complications. Hence, there is a general requirement for risk assessments to consider all possible treatment planning.

 
  References Top

1.
Hirato J, Nakazato Y. Pathology of pineal region tumors. J Neurooncol 2001;54:239-49.  Back to cited text no. 1
    




 

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