Genetic alterations in thyroid carcinoma associated with familial adenomatous polyposis: Clinical implications and suggestions for early detection

Francesco Cetta, Sylviane Olschwang, Margherita Petracci, Giulia Montalto, Claudio Baldi, Michele Zuckermann, Renato Mariani Costantini, Alfredo Fusco

Research output: Contribution to journalArticle

Abstract

Germ-line mutations of the adenomatous polyposis (APC) gene, responsible for familial adenomatous polyposis (FAP) were analyzed in 15 patients with FAP-associated papillary thyroid carcinomas: 13 had the mutation between codons 778 and 1309 (exon 15), 1 at codon 593 (exon 14), and 1 at codon 140 (exon 3). Therefore APC gene mutations clustered in the genomic area associated with congenital hypertrophy of the retinal pigment epithelium (CHRPE) (codons 463-1387). Ocular patches were documented in 12 patients. In particular, 4 of the 15 patients, all women with a mean age of 23.5 (range 20-32), were found during the study of 15 consecutive kindreds who had undergone systematic screening for extracolonic manifestations. Three of them belonged to the same kindred and were asymptomatic. These four patients were also screened for loss of heterozygosity of APC in the thyroid tumoral tissue. No biallelic inactivation of the APC gene was found. In contrast, three of these four patients had activation of the ret-PTC oncogene. In particular, there was activation of the ret-PTC1 isoform, a chimeric gene resulting from fusion of a gene named H4 with the RET gene. On histologic examination, three of the four patients showed Hashimoto-like lymphocytic infiltration. Present data suggest that: (1) the incidence of FAP-associated thyroid cancer probably has been underestimated in the past; (2) intensive screening could detect a larger than expected number of thyroid carcinomas; (3) systematic screening is recommended in patients with ocular patches and genetic mutation in exon 15; (4) Hashimoto-like findings do not exclude carcinoma but are a frequent accompanying finding; (5) despite frequent multicentricity and early lymph node involvement, FAP-associated thyroid tumors seem to have an excellent prognosis, in particular those showing ret- PTC activation.

Original languageEnglish
Pages (from-to)1231-1236
Number of pages6
JournalWorld Journal of Surgery
Volume22
Issue number12
DOIs
Publication statusPublished - Dec 1998

Fingerprint

Adenomatous Polyposis Coli
Thyroid Neoplasms
APC Genes
Codon
Exons
Factor IX
Mutation
Thyroid Gland
Germ-Line Mutation
Retinal Pigment Epithelium
Loss of Heterozygosity
Gene Fusion
Oncogenes
Hypertrophy
Genes
Protein Isoforms
Lymph Nodes
Carcinoma
Incidence

ASJC Scopus subject areas

  • Surgery

Cite this

Genetic alterations in thyroid carcinoma associated with familial adenomatous polyposis : Clinical implications and suggestions for early detection. / Cetta, Francesco; Olschwang, Sylviane; Petracci, Margherita; Montalto, Giulia; Baldi, Claudio; Zuckermann, Michele; Costantini, Renato Mariani; Fusco, Alfredo.

In: World Journal of Surgery, Vol. 22, No. 12, 12.1998, p. 1231-1236.

Research output: Contribution to journalArticle

Cetta, F, Olschwang, S, Petracci, M, Montalto, G, Baldi, C, Zuckermann, M, Costantini, RM & Fusco, A 1998, 'Genetic alterations in thyroid carcinoma associated with familial adenomatous polyposis: Clinical implications and suggestions for early detection', World Journal of Surgery, vol. 22, no. 12, pp. 1231-1236. https://doi.org/10.1007/s002689900550
Cetta, Francesco ; Olschwang, Sylviane ; Petracci, Margherita ; Montalto, Giulia ; Baldi, Claudio ; Zuckermann, Michele ; Costantini, Renato Mariani ; Fusco, Alfredo. / Genetic alterations in thyroid carcinoma associated with familial adenomatous polyposis : Clinical implications and suggestions for early detection. In: World Journal of Surgery. 1998 ; Vol. 22, No. 12. pp. 1231-1236.
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AU - Baldi, Claudio

AU - Zuckermann, Michele

AU - Costantini, Renato Mariani

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