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Article

Villous papillary thyroid carcinoma: a variant associated with marfan syndrome.

Endocrine pathology - 1 Dec 2012

Winer Daniel A, Winer Shawn, Rotstein Lorne, Asa Sylvia L, Mete Ozgur

Abstract excerpt

Marfan syndrome (MFS) is an autosomal dominant hereditary disorder of connective tissue associated with perturbations in transforming growth factor β (TGF-β) biology, most often due to mutations in FBN1 gene that encodes fibrillin-1. To our knowledge, there is no known association of MFS with thyroid carcinoma. We report a 46-year-old man with known history of MFS who developed an unusual histological variant of...

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Source

Identifiers

PMID: 22847364
DOI: 10.1007/s12022-012-9219-6

Genes

BRAF
FBN1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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