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甲状腺乳头状癌转移至间变性脑膜瘤:一例罕见的肿瘤-to-肿瘤转移病例。

Papillary thyroid carcinoma metastasizing to anaplastic meningioma: an unusual case of tumor-to-tumor metastasis.

作者信息

Das Sumit, Chaudhary Navjot, Ang Lee-Cyn, Megyesi Joseph S

机构信息

Division of Neuropathology, London Health Sciences Centre, London, ON, Canada.

Division of Neuropathology, University of Alberta Hospital, Edmonton, AB, Canada.

出版信息

Brain Tumor Pathol. 2017 Jul;34(3):130-134. doi: 10.1007/s10014-017-0289-5. Epub 2017 Jun 9.

DOI:10.1007/s10014-017-0289-5
PMID:28600666
Abstract

Tumor-to-tumor metastasis is a relatively uncommon entity, whereby the so-called 'recipient' tumor is involved by another biologically unrelated 'donor' tumor. Intracranially, meningioma (WHO grade 1) is the most common recipient tumor, while breast and lung cancers are the most common donor tumors. We present an unusual case of intracranial tumor-to-tumor metastasis involving papillary thyroid carcinoma (PTC) believed to have metastasized to an anaplastic meningioma (WHO grade 3). The patient is a 64-year-old female with a history of PTC, whose neuroimaging, performed as part of her staging workup, revealed a right parietal scalp lesion. The lesion was resected to reveal metastatic PTC with spindle cell component believed to represent sarcomatoid differentiation. Follow-up neuroimaging 2 months later revealed regrowth of the lesion under the previous craniotomy site. PET scan showed increased uptake in this area consistent with metastasis. Resection of this lesion revealed primarily features of an anaplastic meningioma. The combination of pathologic findings from both resections in conjunction with findings from the PET scan led to the suggestion that the PTC had metastasized into the anaplastic meningioma. To the authors' knowledge, this is the first example in the literature of a donor tumor metastasizing to a high-grade recipient tumor.

摘要

肿瘤至肿瘤转移是一种相对罕见的情况,即所谓的“受者”肿瘤被另一种生物学上不相关的“供者”肿瘤累及。在颅内,脑膜瘤(世界卫生组织1级)是最常见的受者肿瘤,而乳腺癌和肺癌是最常见的供者肿瘤。我们报告一例罕见的颅内肿瘤至肿瘤转移病例,涉及乳头状甲状腺癌(PTC),据信已转移至间变性脑膜瘤(世界卫生组织3级)。患者为一名64岁女性,有PTC病史,其作为分期检查一部分进行的神经影像学检查显示右侧顶叶头皮病变。该病变切除后显示为伴有梭形细胞成分的转移性PTC,梭形细胞成分被认为代表肉瘤样分化。2个月后的随访神经影像学检查显示原开颅部位下方病变复发。PET扫描显示该区域摄取增加,与转移相符。该病变切除后主要表现为间变性脑膜瘤的特征。两次切除的病理结果与PET扫描结果相结合,提示PTC已转移至间变性脑膜瘤。据作者所知,这是文献中供者肿瘤转移至高级别受者肿瘤的首例。

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