Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Thyroid pathology in PTEN-hamartoma tumor syndrome: characteristic findings of a distinct entity.

Thyroid : official journal of the American Thyroid Association - 1 Feb 2011

Laury Anna Ray, Bongiovanni Massimo, Tille Jean-Christophe, Kozakewich Harry, Nosé Vânia

Abstract excerpt

BACKGROUND: Phosphatase and tensin homolog deleted on chromosome ten (PTEN)-hamartoma tumor syndrome (PHTS) is a complex disorder caused by germline inactivating mutations of the PTEN tumor suppressor gene. PHTS includes Cowden syndrome (CS), Bannayan-Riley-Ruvalcaba syndrome (BRRS), and Proteus-like syndromes. Affected individuals develop both benign and malignant tumors in a variety of tissues, including the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adenocarcinoma, Follicular
Share to Carcinoma, Papillary

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hamartoma Syndrome, Multiple

Share to Hyperplasia

Share to PTEN Phosphohydrolase

Share to Thyroid Cancer, Papillary

Share to Thyroid Gland

Share to Thyroid Nodule

Source

Identifiers

PMID: 21190448
DOI: 10.1089/thy.2010.0226

Genes

PTEN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Thyroid pathology in PTEN-hamartoma tumor syndrome: characteristic findings of a distinct entity.PMID 21190448Read ↗

Abnormal distribution and hyperplasia of thyroid C-cells in PTEN-associated tumor syndromes.Semantic proximity Read ↗

PTEN Hamartoma Tumor Syndrome: A Clinical OverviewSemantic proximity Read ↗

PTEN hamartoma tumor syndrome.Semantic proximity Read ↗

PTEN hamartoma tumor syndromes.Semantic proximity Read ↗

Unmasking familial follicular cell-derived thyroid neoplasms associated with syndromes: DICER1 and PTEN-hamartoma tumor syndromes.Semantic proximity Read ↗

PTEN hamartoma tumor syndrome: clinical risk assessment and management protocol.Semantic proximity Read ↗

PTEN Hamartoma Tumor Syndrome/Cowden Syndrome: Genomics, Oncogenesis, and Imaging Review for Associated Lesions and MalignancySemantic proximity Read ↗

PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocol.Semantic proximity Read ↗

Genetic and phenotypic heterogeneity in the PTEN hamartoma tumour syndrome.Semantic proximity Read ↗

The Genomic Landscape of Benign and Malignant Thyroid Tumors from Individuals Carrying Germline PTEN Variants Is Distinct from Sporadic Thyroid CancersSemantic proximity Read ↗

Insights into Clinical Disorders in Cowden Syndrome: A Comprehensive ReviewSemantic proximity Read ↗

Clinicopathologic features of thyroid nodules with PTEN mutations on preoperative testing.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.