Adrenocortical Carcinoma in Peutz–Jeghers Syndrome With a Rare STK11 Pathogenic Germline Variant: A Case Report
ABSTRACT Background Peutz–Jeghers syndrome (PJS) is an inherited, autosomal‐dominant condition, featuring STK11 germline mutations, characterized by hamartomatous gastrointestinal polyps and increased cancer risk. The most commonly associated malignancies are gastrointestinal, pancreatic, and breast...
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| Autori principali: | , , , , , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Wiley
2026-05-01
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| Serie: | Cancer Reports |
| Soggetti: | |
| Accesso online: | https://doi.org/10.1002/cnr2.70583 |
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