Author:
Sinai Khandeparkar Siddhi Gaurish,Gosavi Shital Subhash,Gogate Bageshri P.,Talathi Nikhil
Abstract
Pilomyxoid astrocytoma (PMA), a distinct clinico-histopathological entity in the World Health Organization classification 2007, tends to be locally aggressive, with higher chance of leptomeningeal dissemination, recurrence, and poor prognosis. PMA is generally seen in young children and tend to occur in the hypothalamic-chiasmatic region. Their presence in other parts of the brain in the non pediatric age group is uncommon. To the best of our knowledge we are presenting first case of cerebellar PMA associated with neurofibromatosis 1 (NF1) in a 40-year- old female, with immunohistochemical study.
Reference10 articles.
1. Pilomyxoid astrocytoma presenting as diencephalic syndrome;Khan;J Ayub Med Coll Abbottabad,2014
2. Pilomyxoid astrocytoma: A review;Komotar;MedGenMed,2004
3. Adult pilomyxoid astrocytoma with hemorrhage in an atypical location;Karthigeyan;Asian J Neurosurg,2019
4. Pilomyxoid astrocytoma in an adult woman: Case report;Kibola;J Can Res Ther,2015
5. The 2016 World Health Organization classification of tumors of the central nervous system: A summary;Louis;Acta Neuropathol,2016
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