CC BY-NC-ND 4.0 · Asian J Neurosurg 2017; 12(03): 566-569
DOI: 10.4103/1793-5482.145547
CASE REPORT

Primary pleomorphic xanthoastrocytoma of the spinal cord: A case report and review of literature

Mayur Sharma
Department of Neurosurgery, Grant Medical College and Sir J.J. Group of Hospitals, Byculla, Mumbai, Maharashtra
,
Vernon Velho
Department of Neurosurgery, Grant Medical College and Sir J.J. Group of Hospitals, Byculla, Mumbai, Maharashtra
,
Rachana Binayake
1   Department of Neuropathology, Grant Medical College and Sir J.J. Group of Hospitals, Byculla, Mumbai, Maharashtra
,
Hrushikesh Kharosekar
Department of Neurosurgery, Grant Medical College and Sir J.J. Group of Hospitals, Byculla, Mumbai, Maharashtra
› Author Affiliations

Primary pleomorphic xanthoastrocytoma (PXA) of the spinal cord is a rare slow growing tumor. To our knowledge, only five such cases have been reported in the literature till date. We report the clinical, radiological, and histopathological features of a spinal PXA in a 23-year-old female previously operated 5 years back for a spinal tumor, presented with weakness in lower limbs, sphincter incontinence and low back pain. Magnetic resonance imaging scan with contrast reveals an intramedullary lesion in the spinal cord from D8-D10 level. The patient was operated with reexploration of the previous incision, and gross total excision was achieved. Histopathology confirmed the diagnosis of PXA. Clinical and radiological follow-up is required to detect early recurrence. Adjunct radiotherapy or and chemotherapy should be considered only when there is postoperative residual or recurrence, however there are no definite guidelines in view of the rarity of this condition.



Publication History

Article published online:
20 September 2022

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