salivary gland malignant tumor

  • 文章类型: Journal Article
    背景:腺泡细胞癌(AcCC),唾液腺的罕见恶性肿瘤,经常复发和转移,特别是在颅底。传统的根治性切除术可以侵入性的颅底AcCC邻近颅神经和主要脉管系统,立体定向放射外科(SRS)作为替代方案的有效性尚不明确。
    方法:本病例报告详细介绍了SRS在复发性颅底AcCC中的应用。一名71岁的男性,有23年前的右下颌AcCC切除史,经历了涉及右海绵窦和鼻腔的肿瘤复发。他接受了鼻内镜手术,然后是针对不同肿瘤位置的SRS-海绵窦至翼腭窝,上颌窦,和clivus-各自的处方剂量为20Gy至40%至50%的等剂量线。在第一次颅底转移后,内镜手术后再进行局部SRS治疗,可获得12年无后遗症的生存期.
    结论:这是一份报告,表明颅底AcCC的SRS可以实现良好的局部控制,功能保存,和长期生存。考虑到病变倾向于多次局部复发,SRS可能适用于颅底AcCC。需要进一步的研究来验证治疗的疗效。
    BACKGROUND: Acinic cell carcinomas (AcCCs), rare malignancies of the salivary glands, often recur and metastasize, particularly in the skull base. Conventional radical resection can be invasive for skull base AcCCs adjacent to cranial nerves and major vasculature, and the effectiveness of stereotactic radiosurgery (SRS) as an alternative is not well established.
    METHODS: This case report details the application of SRS for recurrent skull base AcCCs. A 71-year-old male with a history of resection for a right mandibular AcCC 23 years earlier experienced tumor recurrence involving the right cavernous sinus and nasal cavity. He underwent endoscopic transnasal surgery followed by SRS targeting different tumor locations-the cavernous sinus to the pterygopalatine fossa, maxillary sinus, and clivus-each with a prescribed dose of 20 Gy to the 40% to 50% isodose line. After the first skull base metastasis, additional sessions of localized SRS after endoscopic surgery led to a 12-year survival without sequela.
    CONCLUSIONS: This is a report indicating that SRS for skull base AcCCs can achieve favorable local control, functional preservation, and long-term survival. SRS may be suitable for skull base AcCC given the lesion\'s tendency toward multiple local recurrences. Further investigation is needed to validate the treatment\'s efficacy.
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  • 文章类型: Journal Article
    背景:多形性腺癌(PACs)是由唾液腺引起的罕见肿瘤。根治性切除和术后放疗是治疗的主要手段。然而,当肿瘤侵入颅底时,并不总是可以完全切除肿瘤。立体定向放射外科(SRS)可能是治疗颅底PAC的侵入性较小的替代方法。
    方法:一名70岁男性,有右腭PAC手术史,表现为右视力障碍,复视,和上眼睑。影像学检查显示肿瘤复发侵犯右侧海绵窦(CS)。对于这种复发,使用伽玛刀进行了SRS,在50%的等剂量线处开出18Gy的边际剂量。SRS之后五个月,他的症状缓解了,肿瘤控制良好55个月,无任何不良事件发生.
    结论:据作者所知,这是世界上首例复发性颅底PAC侵犯CS的病例,并成功采用抢救SRS治疗。因此,SRS可能是颅底PAC的适用治疗选择。
    BACKGROUND: Polymorphous adenocarcinomas (PACs) are rare tumors arising from the salivary glands. Radical resection and postoperative radiotherapy are the mainstays of treatment. However, complete tumor resection is not always achievable when the tumor invades the skull base. Stereotactic radiosurgery (SRS) could be a less invasive alternative for treating skull base PACs.
    METHODS: A 70-year-old male with a history of surgery for a right palatine PAC presented with right visual impairment, diplopia, and ptosis. Imaging studies revealed tumor recurrence invading the right cavernous sinus (CS). SRS using a gamma knife was performed for this recurrence, prescribing a marginal dose of 18 Gy at a 50% isodose line. Five months after SRS, his symptoms were relieved, and the tumor was well-controlled for 55 months without any adverse events.
    CONCLUSIONS: To the best of the authors\' knowledge, this is the world\'s first case of recurrent skull base PAC invading the CS that was successfully treated with salvage SRS. Thus, SRS may be an applicable treatment option for skull base PACs.
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  • 文章类型: Journal Article
    目的:为了研究临床表现,病理特征,涎腺恶性肿瘤(SGMT)伴颅底转移的治疗和预后。
    方法:对5例SGMT颅底转移患者进行回顾性研究。主要临床症状包括头痛,面瘫,耳朵听力损失。3例患者既往有SGMT切除史。所有患者均行术前计算机断层扫描(CT)和磁共振成像(MRI)。三名患者进行了开颅手术,5例患者均接受了放疗和化疗。
    结果:两名患者被证实患有腺癌,一名患者经病理证实患有鳞状细胞癌,一名患者患有导管癌,一名患者患有腺泡细胞癌。一名患者在治疗2年后死亡,其余4例患者随访6~24个月,提示肿瘤大小未增大或无局部复发。
    结论:SGMT伴颅底转移极为罕见,由于相似的成像特性,很容易误诊为脑膜瘤或神经鞘瘤。早期诊断,入侵程度,手术和联合化疗和放疗是该疾病的预后因素。
    UNASSIGNED: To investigate the clinical performance, pathological characteristics, treatment and prognosis of salivary gland malignant tumor (SGMT) with skull base metastasis.
    UNASSIGNED: Five SGMT patients with skull base metastasis were retrospectively studied. Major clinical symptoms included headache, facial paralysis, and ear hearing loss. Three patients had previous history of SGMT resection. All patients underwent preoperative computed tomography (CT) and magnetic resonance imaging (MRI). Craniotomy was performed in three patients, and all the five patients underwent radiotherapy and chemotherapy.
    UNASSIGNED: Two patients were confirmed as having adenocarcinoma, one patient was pathologically confirmed to have squamous cell carcinoma, one patient had ductal carcinoma, and one patient had acinar cell carcinoma. One patient died after 2 years of treatment, and the remaining 4 patients were followed up for 6 ∼ 24 months, suggesting that the tumor size was not enlarged or showed no local recurrence.
    UNASSIGNED: SGMT with skull base metastasis is extremely rare, and due to similar imaging characteristics, it can be easily misdiagnosed as meningioma or schwannoma. Early diagnosis, extent of invasion, surgery and combination of chemotherapy and radiotherapy are the prognostic factors of the disease.
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