Suppr超能文献

头颈部副神经节瘤对177Lu-DOTATATE的延迟和持久反应:病例报告与文献综述

Delayed and Long-Lasting Response to 177Lu-DOTATATE in a Head and Neck Paraganglioma: Case Report and Literature Review.

作者信息

Ruffini Egea Sofía, Campos Ramírez Sara Elena, Pascual de la Fuente Natalia Pilar, Monreal Cepero María Luna, Mocha Campillo Fatima, Trincado Cobos Pablo, Antón Torres Antonio, Martínez Trufero Javier

机构信息

Medical Oncology Department, Hospital Universitario Miguel Servet, Zaragoza, Spain.

出版信息

Case Rep Oncol. 2024 Oct 30;17(1):1252-1257. doi: 10.1159/000541359. eCollection 2024 Jan-Dec.

Abstract

INTRODUCTION

Malignant paragangliomas (M-PGL) are a group of neuroendocrine tumors that originate from chromaffin cells. The most common location for PGL is the head and neck, which comprise 65-70% of all PGL, and the M-PGL accounts for 0.6% of all head and neck cancers. It is a rare tumor, with an incidence of 2-8 per million. Diagnosing PGL can be challenging, and treatment for metastatic disease is usually not curative.

CASE PRESENTATION

A 66-year-old woman was diagnosed with left cervical pain and laterocervical mass in March 2015. Octreotide scintigraphy showed intense uptake in the cervical mass, two pulmonary micronodules of 4-5 mm, and another lesion in the lumbar region (L3-L4). The final diagnosis was malignant nonsecretory PGL with adjacent tissue involvement and distant metastases. After three different treatments with minimal symptomatic improvement, 177Lu-DOTATATE was requested off-label. With a dose of 7,400 MBq until January 2018, the patient showed remarkable symptomatic pain improvement and a decrease in tumor size.

CONCLUSION

We believe that our case report provides relevant information that can be considered in similar cases. First, the patient tripled the expected survival in such a clinical setting, and this benefit seems to rely on 177Lu-DOTATATE treatment. Second, we documented an early symptomatic response to this treatment but a long-term delayed volumetric radiographic response.

摘要

引言

恶性副神经节瘤(M-PGL)是一组起源于嗜铬细胞的神经内分泌肿瘤。副神经节瘤最常见的部位是头颈部,占所有副神经节瘤的65%-70%,而M-PGL占所有头颈癌的0.6%。它是一种罕见肿瘤,发病率为百万分之二至八。诊断副神经节瘤具有挑战性,转移性疾病的治疗通常无法治愈。

病例报告

一名66岁女性于2015年3月被诊断为左侧颈部疼痛和颈外侧肿块。奥曲肽闪烁扫描显示颈部肿块、两个4-5毫米的肺微小结节以及腰椎区域(L3-L4)有强烈摄取。最终诊断为恶性非分泌性副神经节瘤,伴有相邻组织受累和远处转移。在三种不同治疗后症状改善甚微,遂超说明书使用177Lu-奥曲肽。至2018年1月,剂量为7400兆贝可,患者症状性疼痛明显改善,肿瘤大小减小。

结论

我们认为我们的病例报告提供了可在类似病例中参考的相关信息。首先,患者在这种临床情况下的生存期是预期的三倍,这种获益似乎依赖于177Lu-奥曲肽治疗。其次,我们记录了该治疗的早期症状反应,但体积的影像学反应延迟较长时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a97/11524611/3098e5a36c7c/cro-2024-0017-0001-541359_F01.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验