Multiple Endocrine Neoplasia Syndromes A Comprehensive Imaging Review

被引：11

作者：

Grajo, Joseph R. ^{[1
]}

Paspulati, Raj Mohan ^{[2
]}

Sahani, Dushyant V. ^{[3
]}

Kambadakone, Avinash ^{[3
]}

机构：

[1] Univ Florida, Coll Med, Dept Radiol, Div Abdominal Imaging,Shands Med Ctr, POB 100374, Gainesville, FL 32610 USA

[2] Case Western Reserve Univ, Univ Hosp Case Med Ctr, Dept Radiol, 11100 Euclid Ave, Cleveland, OH 44106 USA

[3] Harvard Univ, Massachusetts Gen Hosp, Div Abdominal Imaging, Dept Radiol,Sch Med, 55 Fruit St,White 270, Boston, MA 02114 USA

来源：

RADIOLOGIC CLINICS OF NORTH AMERICA | 2016年 / 54卷 / 03期

关键词：

Multiple endocrine neoplasia; MEN1; MEN2; MEN4; Neuroendocrine tumor; DES TUMEURS ENDOCRINES; NEUROENDOCRINE TUMORS; ADRENAL INVOLVEMENT; METAIODOBENZYLGUANIDINE; APPEARANCES; SENSITIVITY; MUTATIONS; SEQUENCES; PANCREAS; SPECTRUM;

D O I：

10.1016/j.rcl.2015.12.001

中图分类号：

R8 [特种医学]; R445 [影像诊断学];

学科分类号：

1002 ; 100207 ; 1009 ;

摘要：

MEN1, MEN2, and MEN4 comprise a series of familial disorders involving the simultaneous occurrence of tumors in more than one endocrine organ, collectively known as multiple endocrine neoplasia. Patients with this family of disorders develop tumors of the parathyroid gland, pancreas, pituitary gland, adrenal gland, and thyroid gland, along with miscellaneous neuroendocrine tumors of the respiratory and gastrointestinal tracts. Although some patients undergo early prophylactic surgical management, particularly in the setting of familial medullary thyroid carcinoma, many develop tumors later in life. These tumors are often discovered at imaging for screening purposes. Recognition of the imaging features of the known tumors is important for appropriate patient management.

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页码：441 / +

页数：12

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