A novel succinate dehydrogenase subunit B gene mutation, H132P, causes familial malignant sympathetic extraadrenal paragangliomas

被引:21
|
作者
Maier-Woelfle, M
Brändle, M
Komminoth, P
Saremaslani, P
Schmid, S
Locer, T
Heitz, PU
Krull, I
Galeazzi, RL
Schmid, C
Perren, A
机构
[1] Univ Zurich Hosp, Dept Pathol, Inst Clin Pathol, CH-8091 Zurich, Switzerland
[2] Univ Zurich Hosp, Dept Internal Med, Div Endocrinol & Diabetol, CH-8091 Zurich, Switzerland
[3] Kantonsspital, Dept Internal Med, CH-9007 St Gallen, Switzerland
[4] Kantonsspital Baden, Inst Pathol, CH-5405 Baden, Switzerland
来源
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 2004年 / 89卷 / 01期
关键词
D O I
10.1210/jc.2003-031236
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report a family with malignant sympathetic paragangliomas (PGL) exhibiting a new type of germline mutation in the succinate dehydrogenase subunit B (SDHB) gene. Two affected brothers, presenting with symptoms at the ages of 25 and 52 yr, suffered from malignant abdominal extraadrenal sympathetic PGL. They died of their disease at ages 43 and 61 yr. Their mother had the same history of signs and symptoms, suggesting a catecholamine-producing tumor at the age of 55 yr. Analysis of the germline DNA from these three patients revealed a novel mutation in exon 4 (H132P) of the SDHB gene. This mutation was absent in 160 control chromosomes. Loss of heterozygosity analysis of the tumors showed a loss of one SDHB allele, and RT-PCR-based expression analysis confirmed the exclusive expression of the mutated allele in both tumors. A review of the published PGL families revealed malignant tumors in seven of 12 well-documented families with SDHB mutation-associated extraadrenal PGL. These findings, as well as findings of the family reported here, suggest a strong causal relationship of SDHB germline mutations with malignant extraadrenal abdominal PGL and imply the necessity of a close follow-up of affected individuals and family members.
引用
收藏
页码:362 / 367
页数:6
相关论文
共 49 条
  • [1] Succinate dehydrogenase subunit B-mutation-related pheochromocytomas and sympathetic paragangliomas: Gene analyses and clinicopathological study
    Kimura, N.
    Takekoshi, K.
    VIRCHOWS ARCHIV, 2013, 463 (02) : 112 - 112
  • [2] The malignant potential of a succinate dehydrogenase subunit B germline mutation
    Fuentes, C.
    Menendez, E.
    Pineda, J.
    Martinez De Esteban, J. P.
    Anda, E.
    Goni, M. J.
    Bausch, B.
    Neumann, H. P. H.
    JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2006, 29 (04) : 350 - 352
  • [3] The malignant potential of a succinate dehydrogenase subunit B germline mutation
    C. Fuentes Gómez
    E. Menéndez
    J. Pineda
    J. P. Martínez De Esteban
    E. Anda
    M. J. Goñi
    B. Bausch
    H. P. H. Neumann
    Journal of Endocrinological Investigation, 2006, 29 : 350 - 352
  • [4] Bilateral Carotid Body Paragangliomas With Succinate Dehydrogenase Complex Subunit D Gene Mutation
    Khan, Abdul R.
    Li, Kelvin
    Gupta, Neel D.
    Gupta, Jagan D.
    Ansari, Mohammed M.
    Do, Triet M.
    Palacios, Enrique
    ENT-EAR NOSE & THROAT JOURNAL, 2025,
  • [5] Biochemically Silent Abdominal Paragangliomas in Patients with Mutations in the Succinate Dehydrogenase Subunit B Gene
    Timmers, Henri J. L. M.
    Pacak, Karel
    Huynh, Thanh T.
    Abu-Asab, Mones
    Tsokos, Maria
    Merino, Maria J.
    Baysal, Bora E.
    Adams, Karen T.
    Eisenhofer, Graeme
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2008, 93 (12): : 4826 - 4832
  • [6] Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas
    Amar, Laurence
    Baudin, Eric
    Burnichon, Nelly
    Peyrard, Severine
    Silvera, Stephane
    Bertherat, Jerome
    Bertagna, Xavier
    Schlumberger, Martin
    Jeunemaitre, Xavier
    Gimenez-Roqueplo, Anne-Paule
    Plouin, Pierre-Francois
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2007, 92 (10): : 3822 - 3828
  • [7] Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas
    Diana E Benn
    Michael S Croxson
    Kathy Tucker
    Christopher P Bambach
    Anne Louise Richardson
    Leigh Delbridge
    Peter T Pullan
    Jeremy Hammond
    Deborah J Marsh
    Bruce G Robinson
    Oncogene, 2003, 22 : 1358 - 1364
  • [8] Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas
    Benn, DE
    Croxson, MS
    Tucker, K
    Bambach, CP
    Richardson, AL
    Delbridge, L
    Pullan, PT
    Hammond, J
    Marsh, DJ
    Robinson, BG
    ONCOGENE, 2003, 22 (09) : 1358 - 1364
  • [9] Bilateral Paragangliomas in the Presence of p.C68Y Variant of the Succinate Dehydrogenase Subunit B (SDHB) Gene
    Subang, Maria Laarni
    Malek, Rana
    Alexander, Henry Richard
    ENDOCRINE REVIEWS, 2014, 35 (03)
  • [10] Compound Heterozygous Mutation With a Novel Splice Donor Region DNA Sequence Variant in the Succinate Dehydrogenase Subunit B Gene in Malignant Paraganglioma
    Majumdar, Suvankar
    Friedrich, Christopher A.
    Koch, Christian A.
    Megason, Gail C.
    Fratkin, Jonathan D.
    Moll, George W.
    PEDIATRIC BLOOD & CANCER, 2010, 54 (03) : 473 - 475