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肺腺癌颅底脊索瘤罕见肿瘤-肿瘤转移。

Rare Tumor-to-Tumor Metastases Involving Lung Adenocarcinoma to Petroclival Meningiomas.

机构信息

Charles E. Schmidt College of Medicine, Florida Atlantic University, Boca Raton, Florida, USA.

Department of Neurosurgery, University of Miami Miller School of Medicine, Miami, Florida, USA.

出版信息

World Neurosurg. 2020 Dec;144:125-135. doi: 10.1016/j.wneu.2020.07.140. Epub 2020 Jul 27.

DOI:10.1016/j.wneu.2020.07.140
PMID:32730974
Abstract

BACKGROUND

Lung carcinoma metastasizing to a skull base meningioma remains an extremely rare phenomenon, with only 3 studies reported. Furthermore, no documented cases have been reported in the petroclival region. Thus, we have presented the first 2 cases of tumor-to-tumor metastasis (TTM) in which a petroclival lesion, initially thought to be purely meningioma, was also found to contain metastatic lung adenocarcinoma.

CASE DESCRIPTION

We present the cases of 2 patients with a known history of lung adenocarcinoma and stable petroclival meningioma who had presented with new-onset neurologic deficits. Repeat imaging studies for both patients found an increased lesion size and peritumoral enhancement; thus, both patients underwent emergent craniotomy for complete lesion resection. Intraoperatively, both lesions had zones of markedly different tumoral texture. On histologic analysis, both lesions showed metastatic lung adenocarcinoma contained within the primary petroclival meningioma.

CONCLUSION

Skull base TTM is a rare entity for which no specific management guidelines have been created. Therefore, even if the imaging characteristics suggest a more benign process, skull base TTM should remain high on the differential diagnosis for patients with a known primary cancer and new-onset, rapidly progressive, neurologic deficits. Close clinical follow-up with short-interval repeat imaging in this subset of patients might prevent misdiagnosis and facilitate prompt treatment.

摘要

背景

肺癌转移至颅底脑膜瘤仍然是一种极为罕见的现象,仅有 3 项研究报道过。此外,在岩斜区也没有报道过有记录在案的病例。因此,我们首次报告了 2 例肿瘤对肿瘤转移(TTM)的病例,其中岩斜区病变最初被认为是单纯脑膜瘤,但也被发现含有转移性肺腺癌。

病例描述

我们报告了 2 例有已知肺腺癌病史和稳定的岩斜脑膜瘤的患者,他们出现了新发的神经功能缺损。对这 2 例患者的重复影像学研究发现病变大小增加且有瘤周增强;因此,这 2 例患者均接受紧急开颅手术以完全切除病变。术中,这 2 个病变有明显不同的肿瘤质地区域。组织学分析显示,这 2 个病变均显示转移性肺腺癌位于原发性岩斜脑膜瘤内。

结论

颅底 TTM 是一种罕见的实体,尚未制定出特定的治疗指南。因此,即使影像学特征提示为良性病变,对于有已知原发性癌症和新发、迅速进展的神经功能缺损的患者,仍应高度怀疑颅底 TTM。对这组患者进行密切的临床随访和短间隔重复影像学检查可能有助于防止误诊并促进及时治疗。

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