Suppr超能文献

甲状旁腺癌——十年谜团之经验

Parathyroid Carcinoma-An Experience of the Enigma Over 10 Years.

作者信息

Nayyar Supreet Singh, Thiagarajan Shivakumar, Chaukar Devendra, Laskar Sarbani Ghosh, Patil Asawari, Mahajan Abhishek, Shah Snehal

机构信息

Department of Head and Neck Surgical Oncology, Homi Bhabha National Institute, Tata Memorial Hospital, Mumbai, Maharashtra, India.

Department of Radiation Oncology, Homi Bhabha National Institute, Tata Memorial Hospital, Mumbai, Maharashtra, India.

出版信息

Indian J Endocrinol Metab. 2020 Mar-Apr;24(2):137-142. doi: 10.4103/ijem.IJEM_588_19. Epub 2020 Apr 30.

Abstract

INTRODUCTION

Parathyroid carcinoma (PC) is an uncommon clinical entity. Identification and appropriate treatment of PC remains a challenge. In this study, we explore clinico-radiological features suggestive of PC, the utility of Castleman's histopathological criteria for the diagnosis of PC and discuss the MD-Anderson prognostic stratification system for PC.

METHODS

Retrospective analysis (case series) of patients who were treated at our tertiary oncology institution between January 2009 and December 2018 with an eventual diagnosis of PC.

RESULTS

The study group comprised 15 patients. The most common presentation was related to the musculoskeletal system ( = 9, 60%). In one of the cases, ultrasound features were recorded to be suspicious of PC. The highest histopathological correlation with PC was found with capsular and vascular invasion ( = 12, 80%). The primary tumor was found in inferior parathyroid glands in most cases ( = 12, 80%). The average tumor size was 2.47 cm. Six patients (40%) received adjuvant radiotherapy (RT). Three patients (20%) developed recurrence, all having distant metastasis. Overall survival (OS) at 3 years was 92.31% and disease-free survival (DFS) of 76.61%.

CONCLUSION

The presence of certain features on ultrasonography might suggest PC preoperatively. Among Castleman's criteria, capsular invasion and vascular invasion had a maximum association with PC in our series. At present, there is no evidence to routinely give adjuvant RT to all patients with PC.

摘要

引言

甲状旁腺癌(PC)是一种罕见的临床实体。甲状旁腺癌的识别和恰当治疗仍然是一项挑战。在本研究中,我们探讨提示甲状旁腺癌的临床放射学特征、卡斯尔曼组织病理学诊断标准对甲状旁腺癌诊断的实用性,并讨论MD安德森甲状旁腺癌预后分层系统。

方法

对2009年1月至2018年12月期间在我们的三级肿瘤机构接受治疗并最终诊断为甲状旁腺癌的患者进行回顾性分析(病例系列研究)。

结果

研究组包括15名患者。最常见的表现与肌肉骨骼系统有关(n = 9,60%)。在其中1例病例中,超声特征被记录为怀疑甲状旁腺癌。与甲状旁腺癌组织病理学相关性最高的是包膜和血管侵犯(n = 12,80%)。大多数病例中,原发性肿瘤位于下甲状旁腺(n = 12,80%)。肿瘤平均大小为2.47厘米。6名患者(40%)接受了辅助放疗(RT)。3名患者(20%)出现复发,均有远处转移。3年总生存率(OS)为92.31%,无病生存率(DFS)为76.61%。

结论

超声检查出现某些特征可能在术前提示甲状旁腺癌。在卡斯尔曼标准中,包膜侵犯和血管侵犯在我们的系列研究中与甲状旁腺癌的关联最大。目前,没有证据表明要对所有甲状旁腺癌患者常规给予辅助放疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13bf/7333759/de7c8e3428f6/IJEM-24-137-g001.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