| Literature DB >> 31470154 |
Hiroshi Uda1, Takehiro Uda2, Kosuke Nakajo1, Yuta Tanoue1, Takahiro Okuno3, Saya Koh1, Yohei Onishi1, Hiroki Ohata1, Yusuke Watanabe1, Ryoko Umaba1, Toshiyuki Kawashima1, Kenji Ohata1.
Abstract
BACKGROUND: Mixed germ cell tumors (MGCTs) usually occur in children. In the present report, we discuss an extremely rare case of adult-onset MGCT composed mainly of yolk sac tumor (YST) around the pineal gland. CASE DESCRIPTION: A 54-year-old Japanese man presented with disturbance of consciousness, Parinaud's syndrome, and gait disturbance. Magnetic resonance imaging revealed a pineal mass lesion, and subtotal resection of the tumor was achieved. The histologic diagnosis was MGCT, consisting mainly of YST. Although he underwent 5 courses of chemotherapy and craniospinal irradiation after surgery, tumor dissemination could not be controlled, and he died 10 months postoperatively.Entities:
Keywords: Adult onset; Mixed germ cell tumor; Pineal region; Yolk sac tumor
Mesh:
Year: 2019 PMID: 31470154 DOI: 10.1016/j.wneu.2019.08.079
Source DB: PubMed Journal: World Neurosurg ISSN: 1878-8750 Impact factor: 2.104