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脑膜瘤与转移性子宫腺癌罕见的颅内碰撞瘤:病例报告及文献复习

A Rare Intracranial Collision Tumor of Meningioma and Metastatic Uterine Adenocarcinoma: Case Report and Literature Review.

作者信息

Merrill Sarah A, Sharma Akanksha, Carlin Rachel E, McCullough Ann E, Porter Alyx B, Bendok Bernard R, Kouloumberis Pelagia E

机构信息

Mayo Clinic Alix School of Medicine, Scottsdale, Arizona, USA.

Department of Neurology, Mayo Clinic, Phoenix, Arizona, USA.

出版信息

World Neurosurg. 2021 Jan;145:340-347. doi: 10.1016/j.wneu.2020.09.108. Epub 2020 Sep 25.

Abstract

BACKGROUND

A collision tumor is a rare entity consisting of 2 histologically distinct tumor types (benign or malignant) in the same anatomic location. This can occur from a tumor-to-tumor metastasis or as a result of 2 adjacent intracranial tumors colliding and growing together. To our knowledge, this is the first reported case of collision tumor with confirmed meningioma and uterine adenocarcinoma. Multiple mechanisms have been proposed for the facilitative growth of collision tumors, including local epigenetic signaling. Clinically, it is important to consider collision tumors in the differential diagnosis of a rapidly growing intracranial lesion in the setting of systemic cancer to provide optimal surgical and postoperative management.

CASE DESCRIPTION

A 78-year-old, right-handed woman with a known 10-year history of stable meningioma presented for evaluation of a right sphenoid wing lesion. She had recently completed treatment of uterine papillary serous carcinoma with no evidence of disease on follow-up imaging. On presentation, there was significant progression of the meningioma resulting in brain compression and right third nerve palsy. The patient underwent urgent resection of the lesion. Pathology demonstrated a collision tumor with a combination of metastatic uterine papillary serous carcinoma and meningioma.

CONCLUSIONS

It is important to consider a collision tumor when a patient with a benign intracranial lesion presents with rapid progression, even in the context of a systemic cancer that rarely metastasizes to the brain. Appropriate histopathologic assessment is crucial in these cases and can have a significant impact on treatment plan and prognosis.

摘要

背景

碰撞瘤是一种罕见的病变,由同一解剖部位的两种组织学上不同的肿瘤类型(良性或恶性)组成。这可能源于肿瘤之间的转移,或者是由于两个相邻的颅内肿瘤碰撞并共同生长所致。据我们所知,这是首例经证实的脑膜瘤与子宫腺癌碰撞瘤病例。对于碰撞瘤的促进生长已提出多种机制,包括局部表观遗传信号。临床上,在系统性癌症背景下,对于快速生长的颅内病变进行鉴别诊断时,考虑碰撞瘤很重要,以便提供最佳的手术及术后管理。

病例描述

一名78岁右利手女性,有已知的10年稳定脑膜瘤病史,因评估右侧蝶骨嵴病变就诊。她近期完成了子宫乳头状浆液性癌的治疗,后续影像学检查未发现疾病迹象。就诊时,脑膜瘤有显著进展,导致脑受压及右侧动眼神经麻痹。患者接受了病变的紧急切除术。病理显示为转移性子宫乳头状浆液性癌与脑膜瘤并存的碰撞瘤。

结论

当患有良性颅内病变的患者出现快速进展时,即使是在很少转移至脑的系统性癌症背景下,考虑碰撞瘤也很重要。在这些病例中,适当的组织病理学评估至关重要,并且可能对治疗方案和预后产生重大影响。

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