Occult Germinoma of the Intramedullary Spinal Cord: A Case Report.

Takumi Hoshimaru, Fugen Takagi, Yuichiro Tsuji, Ryokichi Yagi, Ryo Hiramatsu, Masahiro Kameda, Naosuke Nonoguchi, Motomasa Furuse, Shinji Kawabata, Toshihiro Takami, Masahiko Wanibuchi
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Abstract

Primary germ cell tumors of the central nervous system (CNS) typically occur in the neurohypophysis, hypothalamus, or pineal gland and rarely in the spinal cord. We report a case of a spinal intramedullary tumor, which was first detected on magnetic resonance imaging (MRI) 41 months after the initial symptoms, with a verified pathological diagnosis of germinoma. The initial symptom was an abnormal sensation in the left plantar region that gradually worsened, resulting in severe sensory disturbance, difficulty in standing, and even bladder rectal disturbance. Repeated MRI after the onset failed to provide an imaging diagnosis. The MRI was performed 41 months after the onset and revealed a previously undiagnosed, contrast-enhancing spinal intramedullary neoplastic lesion at the Th11-12 level. Gross total resection of the tumor was successfully performed, and the pathology confirmed the diagnosis of pure germinoma. Postoperative chemotherapy, followed by local radiation, was successfully administered. Among primary germinomas of the CNS, occult germinoma that lacks imaging findings suggestive of tumors in the early stages of onset and becomes apparent over time is often reported as a primary neurohypophyseal germinoma, particularly in adolescents presenting with diabetes insipidus. In the present case, the lesion appeared to correspond to a primary occult germinoma of the intramedullary spinal cord.

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髓内脊髓隐匿性生殖细胞瘤1例报告。
中枢神经系统(CNS)的原发性生殖细胞瘤通常发生在神经垂体、下丘脑或松果体,很少发生在脊髓。我们报告一例脊髓髓内肿瘤,在最初症状41个月后首次在磁共振成像(MRI)上检测到,病理诊断为生殖细胞瘤。最初症状为左足底区感觉异常,逐渐加重,导致严重的感觉障碍,站立困难,甚至膀胱直肠紊乱。发病后反复MRI未能提供影像学诊断。在发病41个月后进行MRI检查,发现Th11-12水平有一个未确诊的脊髓髓内肿瘤病变。肿瘤全切除成功,病理证实为纯粹的生殖细胞瘤。术后化疗,随后局部放疗,成功实施。在中枢神经系统的原发性生殖细胞瘤中,隐匿性生殖细胞瘤在发病早期缺乏肿瘤的影像学表现,随着时间的推移变得明显,通常被报道为原发性神经垂体性生殖细胞瘤,特别是在以尿崩症为表现的青少年中。在本病例中,病变似乎对应于髓内脊髓的原发性隐匿性生殖细胞瘤。
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