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Cowden Syndrome With Gall Bladder Polyps and Incidental Gall Bladder Carcinoma
Cowden syndrome is an uncommon autosomal dominant disorder characterized by multiple hamartomas in various tissues. It is associated with germline mutation in the phosphatase and tensin homolog (PTEN) gene. It has an increased risk of malignancies of various organs (commonly breast, thyroid, and end...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cureus
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313238/ https://www.ncbi.nlm.nih.gov/pubmed/37398799 http://dx.doi.org/10.7759/cureus.39794 |