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E-JCRT CORRESPONDENCE
Year : 2015  |  Volume : 11  |  Issue : 3  |  Page : 667

Pilomyxoid astrocytoma in an adult woman: Case report


1 Department of Medicine, Rutgers New Jersey Medical School, Newark NJ, USA
2 Department of Neurosurgery, Lahey Clinic, Burlington, MA, USA
3 Departments of Surgery, Neuroscience and Experimental Therapeutics, Texas A and M Health Science Center, College of Medicine, The Texas Brain and Spine Institute, Bryan, TX, USA

Correspondence Address:
Shearwood McClelland III
Department of Neurosurgery, Lahey Clinic, 41 Mall Road, Burlington, MA 01805
USA
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0973-1482.138102

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Pilomyxoid astrocytoma (PMA) is a recently classified WHO grade II astrocytoma that is histologically similar to pilocytic astrocytoma (PA). Both tumors typically present in childhood, but PMA is more aggressive with higher rates of recurrence and cerebrospinal fluid dissemination. Currently, there is no standardized treatment protocol for PMA although this will change with increased awareness of this disease entity within the neurosurgical community. We present a 22-year-old patient with a left frontal lobe PMA manifesting with atypical radiographic findings. This is the first reported case of PMA in an adult woman.


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