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

KMT2C mutation in sporadic cribriform morular thyroid carcinoma: A rare case report and review of literature

1 Apr 2025

Abstract excerpt

Cribriform morular thyroid carcinoma is a rare thyroid malignancy with uncertain histogenesis. It predominantly affects young women and is strongly associated with familial adenomatous polyposis. This paper reports a rare case of sporadic cribriform morular thyroid carcinoma in a female patient in her early 50s, with somatic genetic testing revealing a KMT2C mutation. She presented with a solitary lesion confined...

Read the complete abstract on PubMed

Topics

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

Share to Genetic factors in colorectal cancer
Share to Head and Neck Anomalies
Share to Thyroid Cancer Diagnosis and Treatment

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 40173034
DOI: 10.1177/03000605251326789

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

KMT2C mutation in sporadic cribriform morular thyroid carcinoma: A rare case report and review of literaturePMID 40173034Read ↗

Cribriform-morular variant of thyroid carcinoma: a neoplasm with distinctive phenotype associated with the activation of the WNT/β-catenin pathway.Semantic proximity Read ↗

Cribriform-Morular Variant of Papillary Thyroid Carcinoma With Poorly Differentiated Features: A Case Report With Immunohistochemical and Molecular Genetic Analysis.Semantic proximity Read ↗

A unique case of two somatic APC mutations in an early onset cribriform-morular variant of papillary thyroid carcinoma and overview of the literatureSemantic proximity Read ↗

Prevalence, clinicopathologic features, and somatic genetic mutation profile in familial versus sporadic nonmedullary thyroid cancer.Semantic proximity Read ↗

Cribriform-morular variant of papillary carcinoma: the sporadic counterpart of familial adenomatous polyposis-associated thyroid carcinoma. A case report with clinical and molecular genetic correlation.Semantic proximity Read ↗

High-grade cribriform morular thyroid carcinoma: A clinicopathologic analysis of six patients and a review of the literature.Semantic proximity Read ↗

Co-Occurrence of Familial Non-Medullary Thyroid Cancer (FNMTC) and Hereditary Non-Polyposis Colorectal Cancer (HNPCC) Associated Tumors-A Cohort Study.Semantic proximity Read ↗

Thyroid Carcinomas That Occur in Familial Adenomatous Polyposis Patients Recurrently Harbor Somatic Variants in APC , BRAF , and KTM2DSemantic proximity Read ↗

Recognizing Familial Thyroid Neoplasia: The Pathologist's Role in Diagnosis and Management.Semantic proximity Read ↗

Targeted DNA Sequencing Detects Mutations Related to Susceptibility among Familial Non-medullary Thyroid Cancer.Semantic proximity Read ↗

Molecular Pathology of Hereditary and Sporadic Medullary Thyroid CarcinomasSemantic proximity Read ↗

[Hereditary predispositions to follicular thyroid tumors].Semantic proximity Read ↗

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