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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 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 [PDF]

Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2018
non ...
Radio C, Grammatico P
openaire   +4 more sources

Peutz-Jeghers syndrome: revisited

Autopsy and Case Reports, 2022
Vitorino Modesto dos Santos, Lister Arruda Modesto dos Santos, Laura Campos Modesto   +2 more
doaj   +4 more sources

Peutz-Jeghers syndrome

North American Journal of Medical Sciences, 2012
Dear Editor, PeutzJeghers Syndrome (PJS) is an inherited autosomal dominant disorder, and attributed to a mutation localized at 19p13.3.[1] This condition is characterized by mucocutaneous pigmentation and gastrointestinal polyps. The purpose of reporting this case is to remind clinicians that perioral or hand pigmentation should not be taken ...
Parray, Fazl Qadir, Syed, Abdul Wahid, Yatoo, Ghulam Nabi, Zargar, Showkat Ali, Malik, Rayees Ahmad   +4 more
openaire   +4 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