Thyroid Pathology inPTEN-Hamartoma Tumor Syndrome: Characteristic Findings of a Distinct Entity-Reference-Cited by-同舟云学术

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Thyroid Pathology inPTEN-Hamartoma Tumor Syndrome: Characteristic Findings of a Distinct Entity

Published:2011-02 Issue:2 Volume:21 Page:135-144
ISSN:1050-7256
Container-title:Thyroid
language:en
Short-container-title:Thyroid

Author:

Laury Anna Ray¹,Bongiovanni Massimo²,Tille Jean-Christophe²,Kozakewich Harry³,Nosé Vânia¹⁴

Affiliation:

1. Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.

2. Department of Pathology, Hopitaux Universitaire de Geneve, Geneva, Switzerland.

3. Department of Pathology, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts.

4. Department of Pathology, University of Miami Miller School of Medicine, Miami, Florida.

Publisher

Mary Ann Liebert Inc

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.liebertpub.com/doi/pdf/10.1089/thy.2010.0226

Reference47 articles.

1. Localization of the gene for Cowden disease to chromosome 10q22–23

2. Thyroid pathologic findings in patients with Cowden disease

3. Familial Nonmedullary Thyroid Carcinoma

4. Cancer phenomics: RET and PTEN as illustrative models

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1. Analysis of the loss of phosphatase and tensin homolog expression in thyroid tissue for the diagnosis of Cowden syndrome;Surgery;2024-09

2. Can thyroid histomorphology identify patients with PTEN hamartoma tumour syndrome?;Histopathology;2024-07

3. Korean Thyroid Association Guidelines on the Management of Differentiated Thyroid Cancers; Part I. Initial Management of Differentiated Thyroid Cancers - Chapter 4. Pathological Diagnosis and Staging after Thyroidectomy 2024;International Journal of Thyroidology;2024-05-30

4. Thyroid nodules with DICER1 mutation or PTEN alteration: A comparative cytologic, clinical, and molecular study of 117 FNA cases;Cancer Cytopathology;2024-04

5. A New Frameshift Mutation of PTEN Gene Associated with Cowden Syndrome—Case Report and Brief Review of the Literature;Genes;2023-10-05

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