腮腺腺样囊性癌非常晚期颅内肝实质外孤立转移1例并文献复习。

Surgical neurology international Pub Date : 2024-11-15 eCollection Date: 2024-01-01 DOI:10.25259/SNI_403_2024
Hidenori Anami, Tomoko Shiwa, Taku Nonaka, Hiroshi Nakano, Ryosuke Hashimoto, Masatoshi Yamada, Tomonori Kobayashi
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引用次数: 0

摘要

背景:腮腺腺样囊性癌(腺样囊性癌,ACC)常在初次手术后很长时间内表现为远处转移,长期预后较差。最常见的转移部位是肺、肝和骨骼。单次颅内转移非常罕见。病例描述:一名43岁女性,24年前有ACC手术切除史,现表现为Gerstmann综合征和右半盲。头部磁共振成像显示在左枕区有一个孤立的轴外肿瘤。手术切除肿瘤,病理诊断为筛状型ACC转移。由于她没有其他的全身转移,她没有接受辅助治疗,术后35个月没有复发。结论:非常晚期ACC颅内孤立性转移极为罕见。由于病理证实的筛状型ACC有延迟复发的风险,建议长期随访。
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Very late intracranial extraparenchymal solitary metastasis of adenoid cystic carcinoma of the parotid gland: A case report and literature review.

Background: Adenoid cystic carcinoma (ACC) of the parotid gland often manifests as distant metastasis long after the initial surgery, resulting in a poor long-term prognosis. The most common sites of metastasis are the lungs, liver, and bones. Single intracranial metastasis is very rare.

Case description: A 43-year-old woman with a history of surgical removal of ACC 24 years prior presented with Gerstmann syndrome and right hemianopsia. Head magnetic resonance imaging revealed a solitary extra-axial tumor in the left occipital region. The tumor was surgically removed and pathologically diagnosed as a metastasis of cribriform-type ACC. Since she had no other systemic metastasis, she did not receive adjuvant treatment and has remained recurrence-free for 35 months postoperatively.

Conclusion: Very late intracranial solitary metastasis of ACC is extremely rare. Due to the risk of delayed recurrence in pathologically confirmed cribriform type ACC, long-term follow-up is recommended.

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