Results 11 to 20 of about 5,377 (175)

Cancer risk in patients with Peutz–Jeghers syndrome: A retrospective cohort study of 336 cases

Tumor Biology, 2017
Peutz–Jeghers syndrome is a rare autosomal dominant inherited disorder characterized by mucocutaneous pigmentation and hamartomatous gastrointestinal polyposis.
Hong-Yu Chen, Xiao-Wei Jin, Bai-Rong Li, Ming Zhu, Jing Li, Gao-Ping Mao, Ya-Fei Zhang, Shou-Bin Ning   +7 more
doaj   +2 more sources

Peutz-Jeghers Syndrome

Journal of Cutaneous Medicine and Surgery
Peutz-Jeghers syndrome is a rare, hereditary disease defined by the presence of hamartomatous polyps within the gastrointestinal tract (with the exception of the esophagus) and the development of mucocutaneous pigmented lesions, which are most commonly observed in the mouth, buccal mucosa, genitals, periorbital region, and the palm and fingers of the ...
Sherman S, Menon G, Krishnamurthy K.
europepmc   +4 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

A case report of Peutz-Jeghers syndrome in a child with Crohn's disease. [PDF]

JPGN Rep
Abstract Peutz–Jeghers syndrome (PJS) is a rare genetic disorder characterized by hamartomatous polyps and mucocutaneous hyperpigmented freckles, whereas Crohn's disease (CD) is a condition characterized by chronic intestinal inflammation. Here, we present a rare case report of an 11‐year‐old male who presented with both CD and PJS.
Rannulu H, May E, Cunningham B, Cochran E, Zdenek R, Garrity SH.   +5 more
europepmc   +2 more sources

Peutz-Jeghers syndrome [PDF]

Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2018
non ...
Radio C, Grammatico P
openaire   +3 more sources

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