Intracranial teratomas are rare germ cell neoplasms occurring more often during childhood. We report the case of a huge mature teratoma of the pineal region in a 10-year-old patient that was not correctly diagnosed preoperatively by stereotactic biopsy. The tumor was revealed by intracranial hypertension and a Parinaud syndrome. The tumor markers were within normal levels in the serum. A left transcortical parietal approach was used to completely resect the tumor. No adjuvant treatment was given. A complete neurological recovery was observed after the surgical procedure. Follow-up at 2 years did not show any recurrence. Pineal mature teratomas have a good prognosis, in contrast to their immature or mixed counterparts. A rigorous histological examination of the tumor samples is mandatory, in order to not omit a mixed contingent within the tumor. The treatment is exclusively surgical.

1.
Shaffrey ME, et al: Maturation of intracranial immature teratomas. J Neurosurg 1996;85:672–676.
2.
Shokry A, Janzer RC, von Hochstetter AR, Yasargil MG, Hedinger C: Primary intracranial germ-cell tumors: a clinicopathologic study of 14 cases. J Neurosurg 1985;62:826–830.
3.
Konovalov AN, Pitskhelauri DI: Principles of treatment of the pineal region tumors. Surg Neurol 2003;59:250–268.
4.
Jennings MT, Gelman R, Hochberg F: Intracranial germ-cell tumors: natural history and pathogenesis. J Neurosurg 1985;63:155–167.
5.
Kleihues P, Burger PC, Scheithauer BW: Histological Typing of Tumours of the Central Nervous System, ed 2. Berlin, Springer, 1993, p 46.
6.
Naganuma H, et al: Localization of carcinoembryonic antigen in mature intracranial teratomas. J Neurosurg 1985;62:870–873.
7.
Choi JU, Kim DS, Chung SS, Kim TS: Treatment of germ cell tumors in the pineal region. Childs Nerv Syst 1998;14:41–48.
8.
Hanna A, Edan C, Heresbach N, Ben Hassel M, Gueguan Y: Tératome mature évolutif pinéal: à propos d’un cas. Neurochirurgie 2000;46:568–572.
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