Rare RET Variants in a Patient With MEN2A and Multiple Follicular-Derived Thyroid Tumors: A Case Report and Review of the Literature
International Journal of Surgical Pathology
Published online on February 18, 2026
Abstract
International Journal of Surgical Pathology, Volume 34, Issue 5, Page 1295-1302, August 2026.
Multiple endocrine neoplasia (MEN) syndromes are a group of rare autosomal dominant hereditary disorders that are classified into 5 distinct types. MEN2A, the most common type of MEN2, is associated with mutations and variants ofRET, which are ...
Multiple endocrine neoplasia (MEN) syndromes are a group of rare autosomal dominant hereditary disorders that are classified into 5 distinct types. MEN2A, the most common type of MEN2, is associated with mutations and variants ofRET, which are ...