Papillary thyroid carcinoma as first and isolated neoplastic disease in a Lynch syndrome family member with a germline MLH1 mutation

Endocrine. 2022 Jun;77(1):199-202. doi: 10.1007/s12020-022-03048-1. Epub 2022 Apr 12.

Authors

A Verrienti¹, A Carbone², M Sponziello¹, V Pecce¹, D S Cito², R Bruno³

Affiliations

¹ Department of Translational and Precision Medicine, Sapienza University, 00185, Rome, Italy.
² Endocrine Unit, Tinchi Hospital, 75015, Matera, Italy.
³ Endocrine Unit, Tinchi Hospital, 75015, Matera, Italy. roccobruno1@virgilio.it.

PMID: 35415788
DOI: 10.1007/s12020-022-03048-1

No abstract available

Publication types

Letter

MeSH terms

Colorectal Neoplasms, Hereditary Nonpolyposis* / genetics
Colorectal Neoplasms, Hereditary Nonpolyposis* / pathology
DNA Methylation
Family
Genetic Predisposition to Disease
Germ Cells / metabolism
Germ Cells / pathology
Germ-Line Mutation
Humans
MutL Protein Homolog 1 / genetics
MutL Protein Homolog 1 / metabolism
Mutation
Thyroid Cancer, Papillary / genetics
Thyroid Neoplasms* / genetics

Substances

MLH1 protein, human
MutL Protein Homolog 1