1 Department of Neurosurgery HSR, Ibn Sina University Hospital Center in Rabat.
2 Department of Pathology HSR, Ibn Sina University Hospital Center in Rabat.
3 Mohammed V University of Medicine and Pharmacy of Rabat Morocco.
World Journal of Advanced Research and Reviews, 2026, 30(01), 2456-2461
Article DOI: 10.30574/wjarr.2026.30.1.1112
Received on 17 March 2026; revised on 24 April 2026; accepted on 27 April 2026
Background: Pleomorphic xanthoastrocytoma (PXA) is a rare primary tumor of the central nervous system. Anaplasia is defined by a mitotic index of 5 per 10 high-power fields and/or the presence of necrosis. Complete surgical excision and radiochemotherapy are recommended for this entity.
Case presentation: This is a 29-year-old woman with a one-month history of headaches and intracranial hypertension. Imaging revealed a large right basifrontal mass with a double fleshy component and a predominantly cystic appearance. Surgical excision was macroscopically complete. Immunohistological examination confirmed a pleomorphic anaplastic xanthoastrocytoma (grade 3; WHO, 2021).
Conclusions: We report this case to improve the understanding of the clinicoradiological, histopathological, and immunohistochemical features of this rarely encountered tumor.
Anaplastic pleomorphic xanthoastrocytoma; Macroscopic total resection; Immunohistochemistry
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Salma Abbas, EL Mehdi Hakkou, Mohammed Yassaad Oudrhiri, Adil Melhaoui, Nadia Cherradi, Hafsa El Ouazzani and Yasser ARKHA. Uncommun presentation and clinicopathological features of Anaplasic pleomorphic Xanthoastrocytoma: A case report. World Journal of Advanced Research and Reviews, 2026, 30(01), 2456-2461. Article DOI: https://doi.org/10.30574/wjarr.2026.30.1.1112.