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논문 기본 정보

자료유형
학술저널
저자정보
Yoon Do Won (Department of Radiology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seoul, Korea.) Choi Hong-Mi (Division of Cardiology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seoul, Korea.) Song Kyoung-Ho (Division of Infectious Diseases, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seoul, Korea.) Kim Jun Sung (Division of Cardiovascular Surgery, Department of Thoracic and Cardiovascular Surgery, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seoul, Korea) Kong Sung Hye (Division of Endocrinology and Metabolism, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seoul, Korea.) Oh Dongkyu (Department of Nuclear Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seoul, Korea.) Park So Yeon (Department of Pathology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seoul, Korea.) Chun Eun Ju (Department of Radiology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seoul, Korea.)
저널정보
대한자기공명의과학회 Investigative Magnetic Resonance Imaging Investigative Magnetic Resonance Imaging Vol.28 No.2
발행연도
2024.6
수록면
87 - 92 (6page)
DOI
10.13104/imri.2024.0001

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'Paragangliomas, a term used for tumors of extra-adrenal origin, are chromaffin cell tumors that secrete catecholamines. Approximately one in three patients with paraganglioma has a gene mutation associated with familial paraganglioma syndromes (FPGLs), resulting from mutations in one of the subunits of the succinate dehydrogenase (SDH) gene. Most extraadrenal paragangliomas involve the head and neck, and only 2% of paragangliomas are found in the mediastinum. We report the case of a 37-year-old woman with a posterior mediastinal paraganglioma attached to the heart and recurrent glomus jugulare who underwent glomus tumor resection at the age of 17 years. Genetic testing revealed a mutation in the SDH subunit B gene associated with FPGL type 4 (FPGL4). This case report describes the features of multimodal imaging of a posterior mediastinal paraganglioma and explain how a multidisciplinary approach led to the diagnosis of FPGL4.

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