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

页码：166 / 181

页数：16

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