Abstract Background Peutz-Jeghers syndrome (PJS), an autosomal dominant multiple
cancerous disorder, is clinically characterized by mucocutaneous macules and multiple …

Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant genetic disorder characterized
by mucocutaneous pigmentation and multiple hamartomatous polyps in the gastrointestinal …

Peutz–Jeghers syndrome (PJS) is an autosomal dominant genetic disease characterized by
the development of benign hamartomatous polyps in the gastrointestinal tract and …

Abstract Background Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder
characterized by a predisposition to the development of multiple neoplasms. Gastric-type …

Abstract Introduction Patients with Peutz-Jeghers syndrome (PJS) have high risk of
malignancies, including gynecological cancers. Gastric type mucinous cervical …

Peutz-Jeghers syndrome is an autosomal dominant condition characterized by the
association of hamartomatous polyps in the digestive tract, mucocutaneous pigmentation …

Objectives To perform a systematic review of gastric-type adenocarcinoma of the cervix and
lobular endocervical glandular hyperplasia (a possible precursor lesion) in Peutz-Jeghers …

Peutz-Jeghers syndrome (PJS) is an autosomal dominant disorder characterized by the
development of hamartomatous polyposis in the gastrointestinal tract and melanin …

Abstract Background Peutz-Jeghers Syndrome (PJS) is a rare autosomal dominant disorder
characterized by gastrointestinal hamartomatous polyps and mucocutaneous pigmentation …

Background. Peutz-Jeghers Syndrome (PJS) is a rare autosomal dominant condition with
variable penetrance characterized by gastrointestinal hamartomatous polyps and …