Malignant succinate dehydrogenase subunit B-associated paraganglioma in a black African patient

被引：0
|
作者：
Goedhals, J. [1 ]
Shone, D. [1 ]
Pearce, N. [1 ]
机构：
[1] Univ Free State, Dept Anat Pathol, Bloemfontein, South Africa
来源：
VIRCHOWS ARCHIV | 2016年 / 469卷
关键词：
D O I：
暂无
中图分类号：
R36 [病理学];
学科分类号：
100104 ;
摘要：
EPS-05-013
引用
收藏
页码：S255 / S255
页数：1
相关论文
共 50 条
  • [41] Succinate dehydrogenase gene mutations are strongly associated with paraganglioma of the organ of Zuckerkandl
    Lodish, Maya B.
    Adams, Karen T.
    Huynh, Thanh T.
    Prodanov, Tamara
    Ling, Alex
    Chen, Clara
    Shusterman, Suzanne
    Jimenez, Camilo
    Merino, Maria
    Hughes, Marybeth
    Cradic, Kendall W.
    Milosevic, Dragana
    Singh, Ravinder J.
    Stratakis, Constantine A.
    Pacak, Karel
    ENDOCRINE-RELATED CANCER, 2010, 17 (03) : 581 - 588
  • [42] Surgical Management of the Succinate Dehydrogenase-Associated Familial Paraganglioma Syndromes
    Cocieru, Andrei
    Saldinger, Pierre F.
    ARCHIVES OF SURGERY, 2012, 147 (01) : 89 - 91
  • [43] A case report of an intracardiac paraganglioma attached to the left main coronary artery in a patient with a succinate dehydrogenase complex subunit D mutation
    Feijen, Michelle
    Palmen, Meindert
    Lamb, Hildo J.
    Corssmit, Eleonora P. M.
    Antoni, Maria Louisa
    EUROPEAN HEART JOURNAL-CASE REPORTS, 2023, 7 (10)
  • [44] Novel splice donor region dna sequence variant in the succinate dehydrogenase subunit B gene in a boy with malignant paraganglioma in a family with nonclassic congenital adrenal hyperplasia.
    Majumdar, S.
    Friedrich, C.
    Koch, C. A.
    Moll, G. W.
    JOURNAL OF INVESTIGATIVE MEDICINE, 2007, 55 (01) : S251 - S252
  • [45] Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma
    Astuti, D
    Latif, F
    Dallol, A
    Dahia, PLM
    Douglas, F
    George, E
    Sköldberg, F
    Husebye, ES
    Eng, C
    Maher, ER
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (01) : 49 - 54
  • [46] Succinate Dehydrogenase Subunit B (SDHB) Immunohistochemistry Should Not Replace Clinical Genetic Testing for SDHx Mutations in Patients with Pheochromocytoma and Paraganglioma
    Fishbein, L.
    Bennett, B.
    Merrill, S.
    Cohen, D. L.
    LiVolsi, V. A.
    Nathanson, K. L.
    Montone, K.
    NEUROENDOCRINOLOGY, 2014, 99 (3-4) : 289 - 289
  • [47] 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)
  • [48] Succinate Dehydrogenase Subunit B (SDHB) Immunohistochemistry Should Not Replace Clinical Genetic Testing for SDHx Mutations in Patients with Pheochromocytoma and Paraganglioma
    Fishbein, Lauren
    Bennett, Bonita
    Merrill, Shana
    Cohen, Debbie L.
    LiVolsi, Virginia A.
    Nathanson, Katherine L.
    Montone, Kathleen
    PANCREAS, 2014, 43 (03) : 495 - 495
  • [49] 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
    Noriko Kimura
    Jun Saito
    Tetsuo Nishikawa
    Journal of Medical Case Reports, 15
  • [50] Robotic Resection in Succinate Dehydrogenase Subunit B (SDHB)-Mutated Hereditary Paraganglioma: A Case Report of Two Patients and A Literature Review
    Baron, Ekaterina
    Wu, Chih Ching
    Gupta, Kanchan
    Wernberg, Jessica A.
    Sheehan, Michael T.
    Sharma, Rohit
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (03)
12345