Cardiac Paraganglioma Arising From the Right Atrioventricular Groove in a Paraganglioma-Pheochromocytoma Family Syndrome With Evidence of SDHB Gene Mutation: An Unusual Presentation

被引：8

作者：

Del Forno, Benedetto ^{[1
]}

Zingaro, Carlo ^{[1
]}

Di Palma, Enza ^{[1
]}

Capestro, Filippo ^{[1
]}

Rescigno, Giuseppe ^{[1
]}

Torracca, Lucia ^{[1
]}

机构：

[1] Lancisi Cardiol Hosp, Cardiac Surg Div, Via Conca 3, I-60020 Ancona, Italy

来源：

ANNALS OF THORACIC SURGERY | 2016年 / 102卷 / 03期

关键词：

D O I：

10.1016/j.athoracsur.2016.01.072

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Primary cardiac paragangliomas are extremely rare. Recently this neoplasm has been associated with a familiar syndrome as a result of mutation of genes that encode proteins in the mitochondrial complex II. We report a case of a 46-year-old woman having cases of vertebral paraganglioma in her family showing an unusual anatomic and clinical presentation of cardiac paraganglioma and expressing a genetic mutation never associated before with cardiac localization of this neoplasm. (C) 2016 by The Society of Thoracic Surgeons

引用

页码：E215 / E216

页数：2

共 7 条

[1] A Completely Resected Paraganglioma Arising From the Right Atrioventricular Groove
Hu, Min
Pan, Tiecheng
Wei, Xiang
Xiang, Feixiang
ANNALS OF THORACIC SURGERY, 2013, 96 (06): : E137 - E139
[2] 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.
CLINICAL NUCLEAR MEDICINE, 2016, 41 (03) : 204 - 206
[3] A novel mutation in the succinate dehydrogenase subunit D gene in siblings with the hereditary paraganglioma-pheochromocytoma syndrome
Prasad, Chaithra
Oakley, Gerard J., III
Yip, Linwah
Coyne, Christopher
Rangaswamy, Balasubramanya
Dixit, Sanjay B.
SAGE OPEN MEDICAL CASE REPORTS, 2014, 2
[4] Palliation of Extensive Metastatic Bone Disease With 223Ra-Dichloride α-Particle Therapy in a Patient With Malignant Hereditary Paraganglioma-Pheochromocytoma Syndrome With SDHB Mutation
Makis, William
McCann, Karey
McEwan, Alexander J. B.
Sawyer, Michael B.
CLINICAL NUCLEAR MEDICINE, 2016, 41 (02) : 144 - 147
[5] Hereditary pheochromocytoma/paraganglioma syndrome with a novel mutation in the succinate dehydrogenase subunit B gene in a Japanese family: two case reports
Hirose, Rei
Tsurutani, Yuya
Sugisawa, Chiho
Inoue, Kosuke
Suematsu, Sachiko
Nagata, Maki
Hasegawa, Naoki
Kakuta, Yukio
Yonamine, Masato
Takekoshi, Kazuhiro
Kimura, Noriko
Saito, Jun
Nishikawa, Tetsuo
JOURNAL OF MEDICAL CASE REPORTS, 2021, 15 (01)
[6] Hereditary pheochromocytoma/paraganglioma syndrome with a novel mutation in the succinate dehydrogenase subunit B gene in a Japanese family: two case reports
Rei Hirose
Yuya Tsurutani
Chiho Sugisawa
Kosuke Inoue
Sachiko Suematsu
Maki Nagata
Naoki Hasegawa
Yukio Kakuta
Masato Yonamine
Kazuhiro Takekoshi
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Journal of Medical Case Reports, 15
[7] Isolated Cardiac Paraganglioma Encasing Right Coronary Artery With Evidence of Succinyl Dehydrogenase Gene Mutation: Successful Management Using Multimodality Imaging
Garg, Naveen
Pandey, Shashank
Madan, Shiva
Yadav, Subhash
Majumdar, Gurango
Jain, Neeraj
Jain, Manoj
TEXAS HEART INSTITUTE JOURNAL, 2023, 50 (01)

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