Pheochromocytoma in an 8-year-old patient with multiple endocrine neoplasia type 2A: Implications for screening

被引：18

作者：

Rowland, Kathryn J. ^{[1
]}

Chernock, Rebecca D. ^{[2
]}

Moley, Jeffrey F. ^{[1
]}

机构：

[1] Washington Univ, Sch Med, Dept Surg, St Louis, MO 63110 USA

[2] Washington Univ, Sch Med, Dept Pathol, St Louis, MO 63110 USA

来源：

JOURNAL OF SURGICAL ONCOLOGY | 2013年 / 108卷 / 04期

基金：

美国国家卫生研究院;

关键词：

multiple endocrine neoplasia type 2; pheochromocytoma; screening; adrenalectomy; MEDULLARY-THYROID CARCINOMA;

D O I：

10.1002/jso.23378

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Childhood pheochromocytoma in the setting of multiple endocrine neoplasia type 2 (MEN2) remains rare and has not been reported under the age of 12. We present an 8-year-old female with known MEN 2A, C634Y RET mutation, diagnosed with a 6cm pheochromocytoma requiring laparoscopic adrenalectomy. Given this patient's age at diagnosis, screening guidelines should recommend annual screening beginning at age 8 for patients with MEN 2B or MEN 2A codons 630 or 634 RET mutations. J. Surg. Oncol. 2013 108:203-206. (c) 2013 Wiley Periodicals, Inc.

引用

页码：203 / 206

页数：4

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