Parathyroid tumors and related disorders

被引:85
作者
DeLellis, Ronald A. [1 ,2 ,3 ]
机构
[1] Rhode Isl Hosp, Dept Pathol, Providence, RI 02903 USA
[2] Miriam Hosp, Providence, RI 02906 USA
[3] Brown Univ, Warren Alpert Med Sch, Providence, RI 02912 USA
关键词
carcinoma; HPT-JT syndrome; MEN-1; molecular diagnostics; parafibromin; parathyromatosis; Tc-99m-sestamibi; ENDOCRINE NEOPLASIA TYPE-1; FAMILIAL ISOLATED HYPERPARATHYROIDISM; CHRONIC-RENAL-FAILURE; PARAFIBROMIN IMMUNOREACTIVITY; SECONDARY HYPERPARATHYROIDISM; MOLECULAR PATHOGENESIS; SURGICAL-MANAGEMENT; DOUBLE ADENOMAS; CARCINOMA; DISEASE;
D O I
10.1038/modpathol.2010.132
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Primary hyperparathyroidism (P-HPT) is a common endocrine disorder that occurs as a result of adenomas (80-85%), hyperplasias (10-15%) or carcinomas (< 1%) of the parathyroid glands. Molecular genetic analyses of heritable P-HPT syndromes have provided considerable insight into the understanding of sporadic parathyroid tumors and hyperplasias. This review will focus on the criteria for classification of parathyroid proliferative disorders and will highlight our understanding of these lesions at the molecular level. Advances in radiological imaging techniques together with the rapid intraoperative parathyroid hormone assay will be reviewed with respect to current treatment approaches for P-HPT. Modern Pathology (2011) 24, S78-S93; doi:10.1038/modpathol.2010.132
引用
收藏
页码:S78 / S93
页数:16
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