Abstract DICER1 syndrome (OMIM 606241, 601200) is a rare autosomal dominant familial
tumor predisposition disorder with a heterozygous DICER1 germline mutation. The most …

The simple nodular goiter, the etiology of which is multifactorial, encompasses the spectrum
from the incidental asymptomatic small solitary nodule to the large intrathoracic goiter …

Objective: To develop evidence-based recommendations for safe, effective, and appropriate
thyroidectomy. Background: Surgical management of thyroid disease has evolved …

This volume covers tumors of the pituary, the thyroid and parathyroid, the adrenal gland, the
endocrine pancreas, and inherited tumor syndromes. Each entity is extensively discussed …

Answer questions and earn CME/CNE Thyroid cancer exists in several forms. Differentiated
thyroid cancers include those with papillary and follicular histologies. These tumors exist …

Background Constitutional DICER1 mutations were recently reported to cause familial
pleuropulmonary blastoma (PPB). Aim To investigate the contribution and phenotypic …

Context Nontoxic multinodular goiter (MNG) is frequently observed in the general
population, but little is known about the underlying genetic susceptibility to this disease …

The purpose of this review is to summarize current knowledge of the etiology of euthyroid
and toxic multinodular goiter (MNG) with respect to the epidemiology, clinical characteristics …

This review of the familial tumor syndromes involving the endocrine organs is focused on
discussing the main updates on the upcoming fifth edition of the WHO Classification of …

Familial nonmedullary thyroid cancer (FNMTC) is a clinical entity characterized by a
phenotype more aggressive than that of its sporadic counterpart. Families with recurrence of …