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Peutz-Jeghers-Syndrome [PDF]

Pediatric Radiology, 2006
Peutz-Jeghers Syndrome (PJS) is a rare condition that tends to run in families. Diagnosis of PJS is made if a person has polyps in the gastrointestinal (GI) tract and at least two of the following: polyps in the small bowel, melanin spots, and/or a ...
Gowthaman, Gunabushanam, Subramanian, Subramanian, Ashu, Seith   +2 more
core   +4 more sources

Solitary Peutz-Jeghers type hamartomatous polyps in the duodenum are not always associated with a low risk of cancer: two case reports [PDF]

Journal of Medical Case Reports, 2011
Introduction A hamartomatous polyp without associated mucocutaneous pigmentation or a family history of Peutz-Jeghers Syndrome is diagnosed as a solitary Peutz-Jeghers type hamartomatous polyp.
Koide Tomoko, Takahashi Hirokazu, Sakamoto Yasunari, Iida Hiroshi, Tanaka Michio, Tsunemi Akisa, Saito Kumiko, Fujisawa Nobutaka, Takahata Ayako, Akimoto Keiko, Tsuzawa Kaoru, Suzuki Kaori, Hirai Mitsuru, Inamori Masahiko, Sekino Yusuke, Tokoro Chikako, Abe Yasunobu, Nakajima Atsushi, Maeda Shin, Koyama Shigeru   +19 more
doaj   +2 more sources

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

Peutz-Jeghers Syndrome

INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH
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   +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]

Archives of Disease in Childhood, 1980
We report 3 cases of the Peutz-Jeghers syndrome presenting in early childhood, and consider the need for surgical intervention.
C D, Griffith, W H, Bisset
openaire   +2 more sources