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经栓塞和半肝切除术治疗腮腺腺样囊性癌广泛肝转移:1例报告

Management of Extensive Hepatic Metastases From Adenoid Cystic Carcinoma of the Parotid Gland by Embolization and Hemi-Hepatectomy: A Case Report.

作者信息

Desai Gunjan, Lokhande Kaustubh, Parikh Deepak, Wagle Prasad

机构信息

Gastrointestinal Surgery, Lilavati Hospital and Research Centre, Mumbai, IND.

Radiology, Lilavati Hospital and Research Centre, Mumbai, IND.

出版信息

Cureus. 2025 Apr 7;17(4):e81860. doi: 10.7759/cureus.81860. eCollection 2025 Apr.

Abstract

Adenoid cystic carcinoma (ACC) is a rare malignancy of the salivary glands characterized by slow growth, perineural invasion, and a predilection for distant metastasis, primarily to the lungs and bones. Liver metastasis from ACC is uncommon and poses significant diagnostic and therapeutic challenges. This report presents a case of mixed type of ACC (predominantly cribriform and tubular architecture with a solid component of 20%) originating in the parotid gland with multiple liver metastases from a tertiary center in India. A 32-year-old woman initially underwent a total conservative parotidectomy with facial nerve preservation and adjuvant radiotherapy for ACC of the right parotid gland in 2017. Immunohistochemistry was positive for CD117, S100, and smooth muscle actin (SMA). Following a recurrence of metastatic neck lymph node involvement in 2020, she underwent right modified radical neck dissection and additional radiation therapy. In 2024, surveillance imaging revealed liver lesions, confirmed as ACC metastases by biopsy with immunohistochemistry. Due to inadequate hepatic reserve for a right hemi-hepatectomy, a right portal vein embolization was performed to induce hypertrophy of the left liver. Subsequent right hemi-hepatectomy with segment II metastatectomy achieved an R0 resection, and the patient experienced an uneventful recovery. She remained disease-free six months postoperatively. ACC accounts for 1%-2% of all head and neck cancers and exhibits distinct clinical and pathological features. Its treatment is centered on surgical resection with adjuvant radiotherapy, although the efficacy of chemotherapy is limited. Liver metastasis, though rare, can be managed with surgical intervention in selected cases, potentially improving survival outcomes. This case underscores the importance of long-term follow-up for ACC patients due to the risk of delayed distant metastases. It also highlights the role of multidisciplinary management and individualized treatment strategies in achieving optimal outcomes in rare and complex clinical scenarios.

摘要

腺样囊性癌(ACC)是一种罕见的唾液腺恶性肿瘤,其特征为生长缓慢、神经周围浸润,且易发生远处转移,主要转移至肺和骨。ACC发生肝转移并不常见,会带来重大的诊断和治疗挑战。本报告介绍了一例源自印度某三级中心腮腺的混合型ACC(主要为筛状和管状结构,实性成分占20%)并伴有多发肝转移的病例。一名32岁女性于2017年最初接受了保留面神经的右侧腮腺全保守切除术,并接受了右侧腮腺ACC的辅助放疗。免疫组化显示CD117、S100和平滑肌肌动蛋白(SMA)呈阳性。2020年出现转移性颈部淋巴结复发后,她接受了右侧改良根治性颈清扫术及额外放疗。2024年,监测影像显示肝脏有病变,经免疫组化活检确诊为ACC转移。由于肝储备不足无法进行右半肝切除术,遂进行了右门静脉栓塞以诱导左肝肥大。随后进行的右半肝切除术及II段转移灶切除术实现了R0切除,患者恢复顺利。术后六个月她仍无疾病。ACC占所有头颈癌的1%-2%,具有独特的临床和病理特征。其治疗以手术切除并辅以放疗为主,尽管化疗效果有限。肝转移虽罕见,但在某些病例中可通过手术干预进行处理,可能改善生存结局。该病例强调了由于ACC患者存在延迟远处转移的风险,长期随访的重要性。它还凸显了多学科管理和个体化治疗策略在罕见和复杂临床情况下实现最佳治疗效果中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78eb/12059504/7244e8b4a779/cureus-0017-00000081860-i01.jpg

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