Combined Treatment With 131I-MIBG and Sunitinib Induces Remission in a Patient With Metastatic Paraganglioma Due to Hereditary Paraganglioma-Pheochromocytoma Syndrome From an SDHB Mutation

Makis William; McCann Karey; McEwan Alexander J. B.; Sawyer Michael B.

首页> 外文期刊>Clinical nuclear medicine >Combined Treatment With 131I-MIBG and Sunitinib Induces Remission in a Patient With Metastatic Paraganglioma Due to Hereditary Paraganglioma-Pheochromocytoma Syndrome From an SDHB Mutation

【24h】

Combined Treatment With 131I-MIBG and Sunitinib Induces Remission in a Patient With Metastatic Paraganglioma Due to Hereditary Paraganglioma-Pheochromocytoma Syndrome From an SDHB Mutation

机译：131I-MIBG和舒尼替尼的联合治疗可从遗传性副神经节瘤-嗜铬细胞瘤综合征导致的转移性副神经节瘤患者的SDHB突变中缓解

获取原文

获取原文并翻译 | 示例

获取外文期刊封面封底 >>

开具论文收录证明 >>

文献代查 >>

页面导航

摘要
著录项
相似文献
相关主题

摘要

A 22-year-old woman with rapidly progressing metastatic paraganglioma due to hereditary paraganglioma-pheochromocytoma syndrome from an SDHB mutation, who recurred after neoadjuvant chemotherapy, was found to be MIBG avid. She was treated with 2 I-131-MIBG treatments and concurrent sunitinib, achieving a complete response. She was in full remission for 9 months before developing bone metastases.

机译：一名22岁的妇女因新的辅助化疗后复发，由于遗传性副神经节瘤-嗜铬细胞瘤综合征，由于遗传性副神经节瘤-嗜铬细胞瘤综合征而迅速发展，并伴有快速发展的转移性副神经节瘤。她接受了2次I-131-MIBG治疗，并发舒尼替尼，获得了完全缓解。在骨转移之前，她已经完全缓解了9个月。

著录项

来源
《Clinical nuclear medicine》 |2016年第3期|共3页
作者
Makis William; McCann Karey; McEwan Alexander J. B.; Sawyer Michael B.;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类放射医学;
关键词
sunitinib; pheochromocytoma; paraganglioma; I-131-MIBG;

机译：舒尼替尼;嗜铬细胞瘤;副神经节瘤;I-131-MIBG;

相似文献

外文文献
中文文献
专利

1. Combined Treatment With 131I-MIBG and Sunitinib Induces Remission in a Patient With Metastatic Paraganglioma Due to Hereditary Paraganglioma-Pheochromocytoma Syndrome From an SDHB Mutation [J] . Makis William, McCann Karey, McEwan Alexander J. B., Clinical nuclear medicine . 2016,第3期

机译：131I-MIBG和舒尼替尼的联合治疗可从遗传性副神经节瘤-嗜铬细胞瘤综合征导致的转移性副神经节瘤患者的SDHB突变中缓解
2. The utility of SDHB and FH immunohistochemistry in patients evaluated for hereditary paraganglioma-pheochromocytoma syndromes [J] . Aaron M. Udager, Martin J. Magers, Dayna M. Goerke, Human Pathology . 2018,第期

机译：SDHB和FH免疫组织化学术治疗遗传性肺结核瘤 - 嗜铬细胞瘤综合征的效用
3. Pheochromocytoma in a Twelve-Year-Old Girl with SDHB-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome [J] . DarylGraham, MeganGooch, ZhanYe, Case Reports in Genetics . 2014,第2期

机译：与SDHB相关的遗传性副神经节瘤-嗜铬细胞瘤综合征的十二岁女孩的嗜铬细胞瘤
4. The combined approach to treatment of patients witn chronic ischemia and diabetic foot syndrome [C] . Mikhail Smagin, Oleg Shumkov, Rustam Khapaev, Conference on Cognitive Sciences, Genomics and Bioinformatics . 2020

机译：慢性缺血合并糖尿病足综合征的综合治疗
5. Evaluation of the accuracy of quantitative models in predicting Lynch syndrome (hereditary nonpolyposis colorectal cancer with defective DNA mismatch repair) mutations in a population-based sample of early-onset colorectal cancer patients [D] . Carpiniello, Lauren 2007

机译：在以人群为基础的早发性大肠癌患者样本中预测定量模型预测Lynch综合征（遗传性非息肉病性大肠直肠癌，DNA失配修复缺陷）的准确性
6. Pheochromocytoma in a Twelve-Year-Old Girl with SDHB-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome [O] . Daryl Graham, Megan Gooch, Zhan Ye, 2014

机译：与SDHB相关的遗传性副神经节瘤-嗜铬细胞瘤综合征的十二岁女孩的嗜铬细胞瘤
7. The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patients [O] . Bayley, Jean-Pierre, Grimbergen, Anneliese Em, van Bunderen, Patrick A., 2009

机译：副神经节瘤-嗜铬细胞瘤患者中的首次荷兰SDHB创始人删除

Combined Treatment With 131I-MIBG and Sunitinib Induces Remission in a Patient With Metastatic Paraganglioma Due to Hereditary Paraganglioma-Pheochromocytoma Syndrome From an SDHB Mutation

摘要

著录项

相似文献

相关主题

期刊订阅