Endocrine Tumors Associated with Neurofibromatosis Type 1, Peutz-Jeghers Syndrome and Other Familial Neoplasia Syndromes

被引:11
作者
Kalkan, Esra [1 ]
Waguespack, Steven G. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Endocrine Neoplasia & Hormonal Disorders, Houston, TX 77230 USA
来源
ENDOCRINE TUMOR SYNDROMES AND THEIR GENETICS | 2013年 / 41卷
关键词
PAPILLARY THYROID-CARCINOMA; LI-FRAUMENI SYNDROME; ADENOMATOUS POLYPOSIS; TUBEROUS SCLEROSIS; ADRENOCORTICAL CARCINOMA; CLINICAL CHARACTERISTICS; GERMLINE MUTATIONS; ADRENAL MASSES; TP53; MUTATION; APC GENE;
D O I
10.1159/000345676
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Endocrine tumors are a less common but important component of the clinical spectrum of a number of hereditary tumor syndromes such as neurofibromatosis type 1, Peutz Jeghers syndrome, Beckwith-Wiedemann syndrome, the tuberous sclerosis complex, Li-Fraumeni syndrome, PTEN hamartoma tumor syndrome, and APC-associated polyposis. It is important to recognize the often unique clinical presentations of these tumors and possible strategies for presymptomatic screening and early diagnosis. Copyright (C) 2013 S. Karger AG, Basel
引用
收藏
页码:166 / 181
页数:16
相关论文
共 80 条
  • [31] Jasperson KW, 1998, GENEREVIEWS
  • [32] Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase
    Jenne, DE
    Reimann, H
    Nezu, J
    Friedel, W
    Loff, S
    Jeschke, R
    Müller, D
    Back, W
    Zimmer, M
    [J]. NATURE GENETICS, 1998, 18 (01) : 38 - 44
  • [33] Inherited pancreatic endocrine tumor syndromes: Advances in molecular pathogenesis, diagnosis, management, and controversies
    Jensen, Robert I.
    Berna, Marc J.
    Bingham, David B.
    Norton, Jeffrey A.
    [J]. CANCER, 2008, 113 (07) : 1807 - 1843
  • [34] Growth Hormone Excess in Children with Neurofibromatosis Type 1-Associated and Sporadic Optic Pathway Tumors
    Josefson, Jami
    Listernick, Robert
    Fangusaro, Jason R.
    Charrow, Joel
    Habiby, Reema
    [J]. JOURNAL OF PEDIATRICS, 2011, 158 (03) : 433 - 436
  • [35] mTOR expression and activity patterns in gastroenteropancreatic neuroendocrine tumours
    Kasajima, Atsuko
    Pavel, Marianne
    Darb-Esfahani, Silvia
    Noske, Aurelia
    Stenzinger, Albrecht
    Sasano, Hironobu
    Dietel, Manfred
    Denkert, Carsten
    Roecken, Christoph
    Wiedenmann, Bertram
    Weichert, Wilko
    [J]. ENDOCRINE-RELATED CANCER, 2011, 18 (01) : 181 - 192
  • [36] Neurofibromin and NF1 gene analysis in composite pheochromocytoma and tumors associated with von Recklinghausen's disease
    Kimura, N
    Watanabe, T
    Fukase, M
    Wakita, A
    Noshiro, T
    Kimura, I
    [J]. MODERN PATHOLOGY, 2002, 15 (03) : 183 - 188
  • [37] Water-clear cell parathyroid adenoma causing primary hyperparathyroidism in a patient with neurofibromatosis type 1: Report of a case
    Kodama, Hitomi
    Iihara, Masatoshi
    Okamoto, Takahiro
    Obara, Takao
    [J]. SURGERY TODAY, 2007, 37 (10) : 884 - 887
  • [39] Thyroid Pathology in PTEN-Hamartoma Tumor Syndrome: Characteristic Findings of a Distinct Entity
    Laury, Anna Ray
    Bongiovanni, Massimo
    Tille, Jean-Christophe
    Kozakewich, Harry
    Nose, Vania
    [J]. THYROID, 2011, 21 (02) : 135 - 144
  • [40] Zollinger- Ellison syndrome associated with neurofibromatosis type I: a case report
    Lee, WS
    Koh, YS
    Kim, JC
    Park, CH
    Joo, YE
    Kim, HS
    Cho, CK
    Choi, SK
    Rew, JS
    Kim, SJ
    [J]. BMC CANCER, 2005, 5 (1)