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Subcutaneous sacrococcygeal myxopapillary ependymoma

โœ Scribed by Ilhan, Inci; Berberoglu, Semha; Kutluay, Lale; Ata Maden, Hasim

Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
161 KB
Volume
30
Category
Article
ISSN
0098-1532

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โœฆ Synopsis

We report an 8-year-old boy with a primary subcutaneous sacrococcygeal ependymoma, a rare tumor that is thought to arise in embryologic rests. The lesion was completely removed in our patient, who has been followed without recurrence for 20 months. Our experience, together with that of the other 15 cases in the world literature, supports surgical excision as the mainstay of treatment.

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## Abstract Subcutaneous myxopapillary ependymoma in a sacrococcygeal location is an uncommon lesion. We report such a case in a 16โ€moโ€old female child, who presented with a sacrococcygeal mass since birth. The cytological picture was that of a malignant small round cell tumor and the diagnosis was

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