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原发性海绵窦生殖细胞瘤伴非典型扩展模式:一例报告并文献复习

Primary cavernous sinus germinoma with atypical extension pattern: a case report and review of the literature.

作者信息

Sakakura Kazuki, Tsurubuchi Takao, Masumoto Tomohiko, Muroi Ai, Ishikawa Eiichi, Matsumura Akira

机构信息

Department of Neurosurgery, Faculty of Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8575, Japan.

Department of Radiology, Faculty of Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8575, Japan.

出版信息

Childs Nerv Syst. 2019 Sep;35(9):1615-1619. doi: 10.1007/s00381-019-04092-5. Epub 2019 Feb 22.

Abstract

Primary intracranial germinoma is a rare central nervous system tumor that usually arises in the pineal and the supra-sellar region. Here, we report a rare case of primary intracavernous sinus germinoma with an atypical extension pattern, with a comparison to germinomas originating from the cavernous sinus as described in the existing literature. A 12-year-old boy was admitted to our hospital with the chief complaint of the left-side ptosis and double vision. Magnetic resonance imaging showed homogenous enhanced mass lesion in the pineal region together with mass lesions in the lateral ventricle, left cavernous sinus, and temporal lobe, extending into the left masticator space. The enhanced mass in the intracavernous sinus originated from the cavernous sinus. Endoscopic third ventriculostomy and tumor biopsy was done. Pathological diagnosis was pure germinoma. After six courses of chemotherapy followed by radiation therapy, all the lesions decreased in size significantly. Only faint enhancement around the masticator space remained. We report a rare case of a germinoma that developed mainly in the cavernous sinus with additional tumor masses in the pineal region, ventricles, and temporal lobe. Although the lesions shrank significantly on the post-chemoradiation imaging, a long follow-up is necessary not only to check for symptoms, but also monitor imaging findings for possible serial changes in the residual region of the masticator space.

摘要

原发性颅内生殖细胞瘤是一种罕见的中枢神经系统肿瘤,通常发生于松果体区和鞍上区。在此,我们报告一例罕见的原发性海绵窦生殖细胞瘤,其具有非典型的扩展模式,并与现有文献中描述的起源于海绵窦的生殖细胞瘤进行比较。一名12岁男孩因左侧上睑下垂和复视为主诉入院。磁共振成像显示松果体区均匀强化的肿块病变,同时侧脑室、左侧海绵窦和颞叶也有肿块病变,并延伸至左侧咀嚼肌间隙。海绵窦内强化肿块起源于海绵窦。进行了内镜下第三脑室造瘘术和肿瘤活检。病理诊断为纯生殖细胞瘤。经过六个疗程的化疗后进行放疗,所有病变大小均显著减小。仅咀嚼肌间隙周围有轻微强化。我们报告了一例罕见的生殖细胞瘤,主要发生在海绵窦,同时在松果体区、脑室和颞叶有额外的肿瘤肿块。尽管放化疗后的影像学检查显示病变明显缩小,但不仅需要长期随访以检查症状,还需监测影像学表现,以观察咀嚼肌间隙残留区域可能出现的系列变化。

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