Abstract
We present a case of synchronous involvement of the pineal and suprasellar regions by a mixed germ cell tumor comprising germinoma and yolk sac tumor components, with a predominant angiomatous component. To our knowledge, it is the first case of this nature to be reported in the literature. Usually, synchronous lesions of this kind are pure germinomas, and some clinicians will forgo a biopsy and assume a germinoma histology if the serum β-human chorionic gonadotrophin (HCG) is <50 IU/l and the α-fetoprotein (AFP) is within normal limits. Secondly, if a biopsy is performed on a lesion that has a prominent angiomatous component, the diagnostic germ cell tumor may be missed at the time of the biopsy. In order to alert clinicians and pathologists to this rare entity, the case is discussed with particular reference to difficulties that were encountered in rendering an accurate diagnosis, and the associated management implications.
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The authors gratefully acknowledge Michael Jered Kopp for technical assistance during preparation of the figures.
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Cunliffe, C.H., Fischer, I., Karajannis, M. et al. Synchronous mixed germ cell tumor of the pineal gland and suprasellar region with a predominant angiomatous component: a diagnostic challenge. J Neurooncol 93, 269–274 (2009). https://doi.org/10.1007/s11060-008-9770-7
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DOI: https://doi.org/10.1007/s11060-008-9770-7