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Crush Cytologic Findings of Myxopapillary Ependymoma in Spinal Cord: A Case Report.
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HOME > J Pathol Transl Med > Volume 10(1); 1999 > Article
Case Report Crush Cytologic Findings of Myxopapillary Ependymoma in Spinal Cord: A Case Report.
Soo Jin Jung, Young Il Yang
Journal of Pathology and Translational Medicine 1999;10(1):73-78
DOI: https://doi.org/
Department of Pathology, Pusan Paik Hospital, College of Medicine, Inje University, Pusan, Korea.
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Myxopapillary ependymoma generally arise in the conus medullaris and filum terminale of adult spinal cord. These tumors are readily recognized due to unique histopathologic features, however, their cytologic features are not well described. When only a tiny sample is obtained, cytologic examination using crush preparation may be a useful diagnostic tool to help appropriate intraoperative diagnosis. We present the crush cytologic features of myxopapillary ependymoma arising in thoracic and lumbar spinal cord of a 13-year-old boy. The patient had complained of paraparesis and back pain for 1 month. The MRI image revealed a relatively well demarcated intramedullary mass in T11-L1 levels. Crush preparation for cytology were performed by biopsy material. Crush cytologic findings revealed high cellularity and small sized branching papillary clusters on fibrillary or mucinous background. The tumor cells had uniform round or elongated nuclei. The cytoplasmic process of tumor cells were attached to the vascular wall. Between the tumor cells and vascular walls, the perivascular collar of globoid acellular stroma with metachromatic reaction on toluidin blue stain was noted. The crush preparation of myxopapillary ependymoma is considered as a simple and highly accurate diagnostic tool for differentiation from other intramedullary neoplasms of central nervous system.

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