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- W2395087261 abstract "Peutz-Jeghers syndrome (PJS), in most cases, is attributed to mutation in STK11/LKB1 and is clinically characterized by gastrointestinal hamartomatous polyposis, mucocutaneous pigmentation, and predisposition to certain neoplasms. There are currently no recommended gynecologic screening or clinical surveillance guidelines beyond those recommended for the general population; however, cervical cytology samples must be examined with a high level of suspicion for cervical adenocarcinoma. It is considered prudent to note the established association with PJS and recommend referral for genetic counseling. Complete surgical excision after a diagnosis of atypical lobular endocervical glandular hyperplasia is recommended." @default.
- W2395087261 created "2016-06-24" @default.
- W2395087261 creator A5037844254 @default.
- W2395087261 creator A5084467643 @default.
- W2395087261 date "2016-06-01" @default.
- W2395087261 modified "2023-09-28" @default.
- W2395087261 title "Peutz-Jeghers Syndrome" @default.
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- W2395087261 doi "https://doi.org/10.1016/j.path.2016.01.006" @default.
- W2395087261 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27241107" @default.
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