Atypical Pleomorphic Neoplasms of the Pineal Gland: Case Report and Review of the Literature
Overview
Affiliations
Background: Pineal region tumors are rare and diverse. Among them exist reports of pleomorphic xanthroastrocytoma (PXA) and pleomorphic granular cell astrocytoma (PGCA) of the pineal gland. These related tumors are remarkably similar sharing pleomorphic histologic features with only minor immunohistochemical and ultrastructural differences.
Case Description: We present a case of a 42-year old right-handed woman presented with a longstanding history of migraine headaches which had worsened over the two months leading up to her hospitalization. MRI revealed a 1.7 × 1.3 × 1.6 cm intensely enhancing lesion originating in the pineal gland. The tumor closely resembled PGCA but did not strictly fit the diagnostic requirements of either PGCA or PXA.
Conclusion: The present case highlights the exotic nature of pineal region tumors with pleomorphic cell histology. Given the diverse range of tumors encountered in the pineal region, pathological confirmation is mandatory. Favorable clinical outcomes demonstrate that surgical resection alone can yield excellent long-term results for tumors falling within the spectrum of pleomorphic lesions of the pineal gland.
Radiological Insights From Two Distinct Cases of Pineal Region Meningioma: A Case Report.
Ravipati C, Vikram M, Ramakrishnan K, Malaichamy A Cureus. 2024; 16(4):e57796.
PMID: 38721197 PMC: 11077486. DOI: 10.7759/cureus.57796.
Pineal region ganglioglioma: A neoplasm with a bimodal age distribution.
Al-Dalahmah O, Wang L, Hsiao S, Lin C, Mansukhani M, Canoll P Surg Neurol Int. 2022; 13:245.
PMID: 35855114 PMC: 9282777. DOI: 10.25259/SNI_443_2022.
A Rare Case of Atypical Pleomorphic Neoplasm of Pineal Region in a Child: A Case Report.
Kataria S, Neupane K, Ahmed Z, Noor E, Rehman U Cureus. 2020; 12(9):e10515.
PMID: 33094056 PMC: 7571780. DOI: 10.7759/cureus.10515.
Gupta R, Batra V, Jagetia A, Singh D J Neurosci Rural Pract. 2016; 7(3):459-62.
PMID: 27365971 PMC: 4898122. DOI: 10.4103/0976-3147.182780.