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颅内生殖细胞瘤自发消退:病例报告及文献复习。

Spontaneous Regression in Intracranial Germinoma: Case Report and Literature Review.

机构信息

Department of Neurosurgery, West China Hospital of Sichuan University, Chengdu, China.

Department of Neurosurgery, West China Hospital of Sichuan University, Chengdu, China.

出版信息

World Neurosurg. 2019 Nov;131:e32-e37. doi: 10.1016/j.wneu.2019.06.220. Epub 2019 Jul 8.

Abstract

BACKGROUND

Spontaneous regression in intracranial germ cell tumors (GCTs) is an extremely rare phenomenon with only 9 cases reported. The mechanism and natural history of this phenomenon are still equivocal.

METHODS

A 12-year-old boy presented with a lesion in the suprasellar region with involvement of basal ganglia and corpus callosum. After 1 month, his symptoms were relieved, and magnetic resonance imaging demonstrated a remarkable regression of the lesion. Three months later, the boy's symptoms deteriorated, and magnetic resonance imaging revealed regrowth and enlargement of the lesion. Diagnosis of germinoma was confirmed via biopsy, and radiation therapy achieved complete response. We performed a systematic literature review of spontaneous regression of intracranial GCTs. The natural history of these cases was analyzed, and hypotheses in the studies were discussed.

RESULTS

Spontaneous regression is extremely rare with only 10 cases reported, including the present case. There were 9 male patients and 1 female patient with mean age 22.1 ± 10.3 years (range, 12-43 years). Nine cases were diagnosed as germinoma, and 4 cases included an episode of regression followed by regrowth. The mechanism of tumor regression in intracranial GCTs remains unclear. Four hypotheses were proposed, including radiation exposure, surgical procedures, effects of steroids, and immune reaction triggered by intervention.

CONCLUSIONS

Tumor regression in intracranial GCTs could be a iatrogenic transient phenomenon, caused by complex immune reactions triggered by interventions.

摘要

背景

颅内生殖细胞瘤(GCT)自发消退是一种极为罕见的现象,仅有 9 例报告。其机制和自然病程仍存在争议。

方法

一名 12 岁男孩出现鞍上区域病变,累及基底节和胼胝体。1 个月后,他的症状缓解,磁共振成像显示病变明显消退。3 个月后,男孩的症状恶化,磁共振成像显示病变复发和增大。通过活检确诊为生殖细胞瘤,放射治疗达到完全缓解。我们对颅内 GCT 自发消退进行了系统的文献复习。分析了这些病例的自然病程,并讨论了研究中的假设。

结果

自发消退极为罕见,仅有 10 例报告,包括本病例。男性 9 例,女性 1 例,平均年龄 22.1 ± 10.3 岁(范围 12-43 岁)。9 例诊断为生殖细胞瘤,4 例出现消退后复发。颅内 GCT 肿瘤消退的机制尚不清楚。提出了 4 种假说,包括辐射暴露、手术操作、类固醇的作用以及干预触发的免疫反应。

结论

颅内 GCT 的肿瘤消退可能是一种医源性短暂现象,由干预触发的复杂免疫反应引起。

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