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Peutz–Jeghers syndrome with polyps in the stomach, duodenum, and small and large intestine: a case report [PDF]

Journal of Medical Case Reports
Background Peutz–Jeghers syndrome is a rare hereditary condition characterized by gastrointestinal polyps and pigmented oral lesions. The case contributes to a deeper understanding of Peutz–Jeghers syndrome and underscores the significance of ...
Zaryab Ali Shah, Muhammad Zeb, Muhammad Ilyas, Hasnain Hamid, Komal Fatima, Maria Batool, Muhammad Abbas   +6 more
doaj   +2 more sources

Peutz-Jeghers syndrome revealed by CT finding of acute small bowel intussusception: A case report [PDF]

Radiology Case Reports
Peutz-Jeghers syndrome (PJS) is a rare genetic disorder characterized by multiple gastrointestinal hamartomatous polyps and distinctive mucocutaneous pigmentations.
Paola Milillo, MD, PhD, Gianluca Prencipe, MD, Stefano Piscone, MD, Sara Saccone, MD, Luca Cappucci, MD, Maria Grazia Scarale, MD, Roberta Vinci, MD, Luca Macarini, MD, Luca Pio Stoppino, MD, PhD   +8 more
doaj   +2 more sources

A case of multiple small bowel intussusceptions revealing a PEUTZ-JEGHERS syndrome [PDF]

Radiology Case Reports
Peutz-Jeghers Syndrome (PJS) is a rare autosomal dominant disorder marked by mucocutaneous pigmentation and gastrointestinal hamartomatous polyps, with a predisposition to malignancy.
Khaoula Boumeriem, MD, Kabila Badr, MD, Moatassim Billah Nabil, PhD, Nassar Ittimade, PhD, Imrani Kaoutar, PhD   +4 more
doaj   +2 more sources

Clarification of the clinical significance of an intron variant in a case of Peutz–Jeghers syndrome with abnormal RNA splicing of STK11 [PDF]

Molecular Cytogenetics
Peutz–Jeghers syndrome is an autosomal dominant disease characterized by intestinal polyposis, mucocutaneous pigmentation, and an increased risk of various types of cancer.
Aki Ishikawa, Masahiro Gotoh, Mineko Ushiama, Hiromi Sakamoto, Noriko Tanabe, Tomoko Watanabe, Hourin Cho, Masayoshi Yamada, Kokichi Sugano, Kouya Shiraishi, Makoto Hirata, Teruhiko Yoshida, Akihiro Sakurai   +12 more
doaj   +2 more sources

Solitary Peutz-Jeghers type harmartomatous polyp in duodenum with gastric foveolar epithelium: a case report [PDF]

Journal of Pathology and Translational Medicine, 2023
Peutz-Jeghers type hamartomatous polyp is known to be associated with Peutz-Jeghers syndrome, which shows characteristic multiple hamartomatous polyp involvement in the gastrointestinal tract, combined with mucocutaneous symptom, familial history of ...
Eugene Choi, Junghwan Lee, Youngsoo Park
doaj   +1 more source

Peutz–Jeghers syndrome revealed by recurrent small bowel intussusceptions in children: A case report

Clinical Case Reports, 2022
Peutz–Jeghers syndrome is a rare but potentially life‐threating syndrome. We report here the case of a young girl who presented recurrent small bowel intussusceptions.
Chtourou Rahma, Ben Kraiem Najoua, Zouari Mohamed, Mellouli Manel, Dghaies Rim, Ben Dhaou Mahdi, Sellami Boudawara Tahya, Mhiri Riadh   +7 more
doaj   +1 more source

A rare case of gastric-type mucinous adenocarcinoma in a woman with Peutz-Jeghers syndrome [PDF]

Obstetrics & Gynecology Science, 2019
Adenocarcinoma of the cervix is less common than squamous cell carcinoma. Minimal deviation adenocarcinoma (adenoma malignum) is considered an extremely well-differentiated variant of GAS.
Yeorae Kim, Eun Yi Kim, Tae Jin Kim, Kyung Taek Lim, Ki Heon Lee, Yikyeong Chun, Kyeong A So   +6 more
doaj   +1 more source

High Grade Dysplastic Villous Adenoma Arising from a Giant Hamartomatous Polyp- A Rare Case Presentation [PDF]

Journal of Clinical and Diagnostic Research, 2022
Adenomatous polyps can be found throughout the colon, most commonly in right colon. Microscopically they are classified as tubular, villous or tubulovillous subtypes.
Sayan Bhowmik, J Thanka, Rajendran Shanmugasundaram   +2 more
doaj   +1 more source

Peutz-Jeghers syndrome a review of gynecological implications and the management of these patients through the presentation of a case report

Clinical and Experimental Obstetrics & Gynecology, 2022
Background: Peutz-Jeghers Syndrome (PJS) is a rare autosomal dominant genetic condition caused by mutations in STK11 (Serine/threonine kinase 11) gene (OMIM 602216 Serine/Threonine Protein Kinase 11) located in the short arm of chromosome 19 (19p.13.3 ...
Katarzyna Plagens-Rotman, Grażyna Jarząbek-Bielecka, Piotr Merks, Katarzyna Wróblewska-Seniuk, Małgorzata Mizgier, Ewa Jakubek, Samuel Grześkiewicz, Małgorzata Wójcik, Witold Kędzia   +8 more
doaj   +1 more source

The Importance of Simultaneous Surgical and Endoscopic Polypectomies in Peutz-Jeghers Syndrome: A Case Report

İstanbul Medical Journal, 2020
Peutz-Jeghers syndrome may be presented with gastrointestinal and extra-intestinal malignancies. Herein, we report a case of Peutz-Jeghers syndrome with a malignant intestinal polyp accompanied by synchronous multiple hamartomatous gastrointestinal ...
Damla Beyazadam, Tunç Eren, Aman Gapbarov, Hatice Şeneldir, İbrahim Ali Özemir, Özgür Ekinci, Orhan Alimoğlu   +6 more
doaj   +1 more source