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成人患者的多灶性原发性颅内卵黄囊瘤:一例报告及文献复习

Multifocal primary intracranial yolk sac tumor in an adult patient: a case report and literature review.

作者信息

Yang Xiaochen, Wang Yubo, Chen Geng, Hong Xinyu

机构信息

Department of Neurosurgery, First Hospital of Jilin University, Changchun, China.

Department of Neurosurgery, Heze municipal hospital, Heze, China.

出版信息

Transl Cancer Res. 2022 May;11(5):1429-1433. doi: 10.21037/tcr-21-2561.

Abstract

BACKGROUND

Yolk sac tumor is a type of germ cell tumor. It commonly arises in the gonads but sometimes can occur outside the gonads. Primary intracranial yolk sac tumors were very rare. It is always located in the pineal, suprasellar and posterior third ventricular region. The incidence of yolk sac tumor is estimated as less than 8% of all primary intracranial germ cell tumors. Multifocal primary intracranial yolk sac tumors have seldom been reported.

CASE DESCRIPTION

Here we reported a 29 years old male patient with a sudden coma and a history of headaches for one month. Computed Tomography and magnetic resonance imaging of the head showed three masses located at the suprasellar region, pineal region and left temporal lobe separately. The mass at the left temporal lobe was successfully resected with emergency surgery, and decompressive craniectomy was also performed. Intraoperative findings revealed that the tumor was a solid mass with intra-tumoral haemorrhage. The pathology examination confirmed the diagnosis of yolk sac tumor. Hematoxylin and eosin staining clearly showed the Schiller-Duval body. Whole-brain radiotherapy was performed after the operation, and the patient died in a local hospital 11 months after the surgery.

CONCLUSIONS

We reported a case of multifocal primary intracranial yolk sac tumor in an adult patient. Then we reviewed the literature and discussed the treatment and diagnosis of patients with primary intracranial yolk sac tumors.

摘要

背景

卵黄囊瘤是一种生殖细胞肿瘤。它通常起源于性腺,但有时也可发生在性腺外。原发性颅内卵黄囊瘤非常罕见。它总是位于松果体区、鞍上区和第三脑室后部区域。卵黄囊瘤的发病率估计占所有原发性颅内生殖细胞肿瘤的不到8%。多灶性原发性颅内卵黄囊瘤鲜有报道。

病例描述

我们报告了一名29岁男性患者,突发昏迷,有1个月头痛病史。头部计算机断层扫描和磁共振成像显示分别位于鞍上区、松果体区和左颞叶的三个肿块。左颞叶肿块通过急诊手术成功切除,并进行了减压颅骨切除术。术中发现肿瘤为实性肿块,伴有瘤内出血。病理检查确诊为卵黄囊瘤。苏木精-伊红染色清楚地显示了席勒-杜瓦尔小体。术后进行了全脑放疗,患者在手术后11个月死于当地医院。

结论

我们报告了一例成年患者的多灶性原发性颅内卵黄囊瘤病例。然后我们回顾了文献并讨论了原发性颅内卵黄囊瘤患者的治疗和诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9631/9189240/4c1f88da6e84/tcr-11-05-1429-f1.jpg

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