Familial non-medullary thyroid carcinoma: an update (Q37302842)

19 August 2017

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title

Familial non-medullary thyroid carcinoma: an update (English)

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19 August 2017

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Vânia Nosé

1

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19 August 2017

1 January 2008

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19 August 2017

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19 August 2017

19

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19 August 2017

4

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19 August 2017

226-240

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https://scigraph.springernature.com/pub.10.1007/s12022-008-9045-z

19 August 2017

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Familial nonmedullary thyroid cancer. An emerging entity that warrants aggressive treatment.

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Familial nonmedullary thyroid neoplasia

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Does familial non-medullary thyroid cancer adversely affect survival?

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Solitary, multiple, and familial oxyphil tumours of the thyroid gland

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Molecular genetics of thyroid cancer: implications for diagnosis, treatment and prognosis

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Somatic mutations of the ret protooncogene in sporadic medullary thyroid carcinoma are not restricted to exon 16 and are associated with tumor recurrence

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12 December 2020

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome

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Mutational analysis of the APC gene in cribriform-morula variant of papillary thyroid carcinoma.

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PAX8-PPARgamma rearrangement in thyroid tumors: RT-PCR and immunohistochemical analyses

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Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic loci.

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Familial Occurrence of Differentiated (Non-Medullary) Thyroid Cancer

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Molecular profile and clinical-pathologic features of the follicular variant of papillary thyroid carcinoma. An unusually high prevalence of ras mutations.

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RET/PTC rearrangement in thyroid tumors

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Pathologic diagnosis of papillary thyroid carcinoma: today and tomorrow

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Familial nonmedullary thyroid cancer

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Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2.

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Increasing incidence of thyroid cancer in the United States, 1973-2002

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Two families with an autosomal dominant inheritance pattern for papillary carcinoma of the thyroid

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Prophylactic thyroidectomy in multiple endocrine neoplasia type 2A.

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Thyroid pathologic findings in patients with Cowden disease

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Papillary thyroid carcinoma associated with papillary renal neoplasia: genetic linkage analysis of a distinct heritable tumor syndrome

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Familial adenomatous polyposis associated thyroid carcinoma: a distinct type of follicular cell neoplasm

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RET/PTC rearrangements and BRAF mutations in thyroid tumorigenesis

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Alterations of the BRAF gene in thyroid tumors.

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Familial Nonmedullary Thyroid Cancer

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Familial nonmedullary thyroid carcinoma characterized by multifocality and a high recurrence rate in a large study population

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Familial thyroid cancer

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Medullary and papillary tumors are frequently associated in the same thyroid gland without evidence of reciprocal influence in their biologic behavior

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Familial multiple endocrine neoplasia: the first 100 years

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RAS point mutations and PAX8-PPAR gamma rearrangement in thyroid tumors: evidence for distinct molecular pathways in thyroid follicular carcinoma.

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Cribriform-morular variant of papillary carcinoma: a distinctive variant representing the sporadic counterpart of familial adenomatous polyposis-associated thyroid carcinoma?

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Familial risks for nonmedullary thyroid cancer.

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Carcinoma of the thyroid and other diseases of the thyroid in identical twins

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Difference between familial and sporadic medullary thyroid carcinomas

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On the prevalence of familial nonmedullary thyroid cancer in multiply affected kindreds

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Cribriform-morular variant of papillary thyroid carcinoma: a pathological and molecular genetic study with evidence of frequent somatic mutations in exon 3 of the beta-catenin gene

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Familial papillary thyroid microcarcinoma: a new clinical entity

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Unusual features of thyroid carcinomas in Japanese patients with Werner syndrome and possible genotype-phenotype relations to cell type and race

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Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinoma

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12 December 2020

Familial nonmedullary thyroid carcinoma

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12 December 2020

Familial nonmedullary thyroid cancer: an emerging entity that warrants aggressive treatment

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The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

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Medullary thyroid carcinoma: clinical characteristics, treatment, prognostic factors, and a comparison of staging systems

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12 December 2020

Chromosomal aberrations by comparative genomic hybridization in thyroid tumors in patients with familial nonmedullary thyroid cancer

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Excess of rare cancers in Werner syndrome (adult progeria)

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12 December 2020

Familial non-medullary thyroid carcinoma: pathology review in 27 affected cases from 13 French families

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12 December 2020

Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers

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Abnormal distribution and hyperplasia of thyroid C-cells in PTEN-associated tumor syndromes.

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12 December 2020

Cancer phenomics: RET and PTEN as illustrative models

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Analysis of RET protooncogene point mutations distinguishes heritable from nonheritable medullary thyroid carcinomas

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12 December 2020

Increased incidence of thyroid carcinoma in france: a true epidemic or thyroid nodule management effects? Report from the French Thyroid Cancer Committee

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12 December 2020

Familial papillary thyroid carcinoma: genetics, criteria for diagnosis, clinical features, and surgical treatment

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12 December 2020

High prevalence of BRAF mutations in thyroid cancer: genetic evidence for constitutive activation of the RET/PTC-RAS-BRAF signaling pathway in papillary thyroid carcinoma

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12 December 2020

A new form of familial multi-nodular goitre with progression to differentiated thyroid cancer.

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12 December 2020

Enhanced B-Raf protein expression is independent of V600E mutant status in thyroid carcinomas

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12 December 2020

Is familial non-medullary thyroid carcinoma more aggressive than sporadic thyroid cancer? A multicenter series

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12 December 2020

Familial medullary thyroid carcinoma and C cell hyperplasia

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12 December 2020

Simultaneous occurrence of medullary carcinoma and papillary microcarcinoma of thyroid in a patient with MEN 2A syndrome. report of a case

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12 December 2020

Familial papillary thyroid carcinoma is genetically distinct from familial adenomatous polyposis coli

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12 December 2020

Physiologic versus neoplastic C-cell hyperplasia of the thyroid: separation of distinct histologic and biologic entities

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12 December 2020

Genetic heterogeneity in familial nonmedullary thyroid carcinoma: exclusion of linkage to RET, MNG1, and TCO in 56 families. NMTC Consortium.

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12 December 2020

BRAF mutations in thyroid tumors are restricted to papillary carcinomas and anaplastic or poorly differentiated carcinomas arising from papillary carcinomas

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12 December 2020

Pathogenetic mechanisms in thyroid follicular-cell neoplasia

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12 December 2020

A Comprehensive Analysis ofMNG1,TCO1,fPTC,PTEN,TSHR, and TRKA in Familial Nonmedullary Thyroid Cancer: Confirmation of Linkage to TCO1

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12 December 2020

The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndrome

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12 December 2020

Prognostic significance of somatic RET oncogene mutations in sporadic medullary thyroid cancer: a 10-year follow-up study.

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12 December 2020

PTEN: one gene, many syndromes

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12 December 2020

Occult papillary thyroid carcinoma in the young and the aged

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12 December 2020

Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21

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12 December 2020

The role of PTEN, a phosphatase gene, in inherited and sporadic nonmedullary thyroid tumors

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12 December 2020

Pathology and genetics of thyroid carcinoma

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12 December 2020

C cell hyperplasia/neoplasia

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12 December 2020

Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation

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12 December 2020

A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

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12 December 2020

Microcarcinoma of the thyroid

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12 December 2020

BRAF in papillary thyroid carcinoma of ovary (struma ovarii)

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12 December 2020

Early Malignant Progression of Hereditary Medullary Thyroid Cancer

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12 December 2020

Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer

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12 December 2020

At least three genes account for familial papillary thyroid carcinoma: TCO and MNG1 excluded as susceptibility loci from a large Tasmanian family

1 reference

12 December 2020

Thyroid gland abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas (Carney complex)

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12 December 2020

Germline mutations of the APC gene in patients with familial adenomatous polyposis-associated thyroid carcinoma: results from a European cooperative study

1 reference

12 December 2020

Occult papillary carcinoma of the thyroid. A "normal" finding in Finland. A systematic autopsy study

1 reference

12 December 2020

The T1799A BRAF mutation is not a germline mutation in familial nonmedullary thyroid cancer.

1 reference

12 December 2020

Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinomas

1 reference

12 December 2020

A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2.

1 reference

12 December 2020

Carney Complex, Peutz-Jeghers Syndrome, Cowden Disease, and Bannayan-Zonana Syndrome Share Cutaneous and Endocrine Manifestations, But Not Genetic Loci

1 reference

12 December 2020

10.1007/S12022-008-9045-Z

Identifiers

DOI

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19 August 2017

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PubMed ID

18931957