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Information Journal Paper

Title

Case Report: A Rare Case of Sacrococcygeal Teratoma with Medullar Invasion

Pages

  0-0

Abstract

 Background and Importance: Sacrococcygeal teratoma (SCT) with medular invasion is rare. Case Presentation: We report a case of an 11-months male infant, with no prenatal history of any abnormality, presenting since birth, a mass in the buttock extended to retrorectum associated with a right side hypotonic limb and monoplegia. Medullar and abdominal pelvic magnetic resonance imaging (MRI) showed a sacrococcygeal tissue mass and intradural lombosacral invasion with a high level of alpha-fetoprotein. Surgical performed was done successfully with an uneventful follow-up. Conclusion: Although the intradural invasion, those SCT are in major cases mature and present low risk of malignancy or recurrence.

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    APA: Copy

    ABALLA, NAJOUA, Ghannane, Houssine, & Oulad Saiad, Mohammed. (2020). Case Report: A Rare Case of Sacrococcygeal Teratoma with Medullar Invasion. IRANIAN JOURNAL OF NEUROSURGERY, 6(4 (23) ), 0-0. SID. https://sid.ir/paper/667219/en

    Vancouver: Copy

    ABALLA NAJOUA, Ghannane Houssine, Oulad Saiad Mohammed. Case Report: A Rare Case of Sacrococcygeal Teratoma with Medullar Invasion. IRANIAN JOURNAL OF NEUROSURGERY[Internet]. 2020;6(4 (23) ):0-0. Available from: https://sid.ir/paper/667219/en

    IEEE: Copy

    NAJOUA ABALLA, Houssine Ghannane, and Mohammed Oulad Saiad, “Case Report: A Rare Case of Sacrococcygeal Teratoma with Medullar Invasion,” IRANIAN JOURNAL OF NEUROSURGERY, vol. 6, no. 4 (23) , pp. 0–0, 2020, [Online]. Available: https://sid.ir/paper/667219/en

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