Results 21 to 30 of about 5,184 (174)

Peutz-Jeghers sendromu

Ege Tıp Dergisi, 2016
Peutz-Jeghers sendromu (PJS), otozomal dominant gecis gosteren, mukokutanoz pigmentasyon ve gastrointestinal poliplerin goruldugu bir hastaliktir. Yuvarlak, oval, duzgun olmayan, 1-5 mm capindaki kahverengi pigmentasyonlar oral mukoza, dis eti, damak ve dudaklarda yerlesim gosterir.
Yılmaz, Tuğba Han, Avcı, Tevfik, Erol, Varlık, Gülay, Hüseyin   +3 more
openaire   +2 more sources

Peutz-Jeghers Type Polyp of the Appendix with Review of Literature

Case Reports in Pathology, 2019
Hamartomatous polyps of Peutz-Jeghers type are strongly associated with Peutz-Jeghers polyposis syndrome and are predominantly encountered in the small intestine. Sporadic cases are uncommonly reported. We report a case of a polyp identified incidentally
Jolanta Jedrzkiewicz, Keith Quencer, Anna P. Matynia, Ellen Morrow, Maria Pletneva, Gonzalo Barraza   +5 more
doaj   +1 more source

Rare cases of Peutz-Jeghers syndrome in children

Сучасна педіатрія: Україна
Peutz-Jeghers syndrome is a genetic disease in which hamartomatous polyps of the gastrointestinal tract are detected, which leads to an elevated risk of developing colon cancer and other organs.
M.G. Melnychenko, V.O. Sytnikova, N.A. Dybchynska, L.B. Eliy   +3 more
doaj   +1 more source

Melæna massif révélant un syndrome de Peutz-Jeghers vu au CHU-JRA Madagascar: à propos d'un cas

The Pan African Medical Journal, 2016
Le syndrome de Peutz-Jeghers (SPJ) est caractérisé par l'association d'une polypose digestive hamartomateuse et d'une lentiginose cutanéo-muqueuse. Les malades sont exposés à des complications mécaniques et hémorragiques.
Andrianimaro Florelia Martinetti, Rasoanaivo Mamy Andriantsoa, Rajaonera Tovohery Andriambelo, Rakotoarison Ratsaraharimanana Cathérine Nicole, Raveloson Nasolotsiry Enintsoa   +4 more
doaj   +1 more source

Intraoperative endoscopy-assisted tumor debulking in pediatric peutz-jeghers syndrome with early onset massive polyp burden phenotype

Journal of Pediatric Surgery Case Reports, 2022
Peutz-Jeghers Syndrome is an autosomal dominant disorder linked to abnormalities in STK11, and is associated with mucocutaneous pigmentation, sex cord tumors, and gastrointestinal polyps. While it is extremely rare in children under the age of 2, several
Maria E. Tecos, Matthew Ballweg, Andrew Huang-Pacheco, Angela Hanna, Abdalla Zarroug, Patrick Thomas   +5 more
doaj   +1 more source

Peutz-Jeghers syndrome, telangiectasias, and mitral valve prolapse. Case presentation and genetic counseling

Revista Habanera de Ciencias Médicas, 2021
Introduction: Peutz-Jeghers syndrome is characterized by mucocutaneous hyperpigmentation and gastrointestinal hamartomas that can appear from the stomach to the anus. It has an autosomal dominant inheritance pattern and variable expressiveness.
Ana Elena Arús Fernández, Enrique Arús Soler   +1 more
doaj  

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

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   +1 more source

Solitary Peutz Jeghers Polyp Causing Jejunal-Jejunal Intussusception in 6-Year-Old Female Child [PDF]

National Journal of Laboratory Medicine, 2013
Peutz-Jeghers Syndrome (PJS) is a rare autosomal dominant syndrome characterised by the familial occurrence of gastrointestinal hamartomatous polyps in association with mucocutaneous hyperpigmentation.
Khushboo Birla, Sunita Sanjay Dantkale, Hemlata Kamra, Pankaj W. Sakinlawar, Swapnil D. Chandekar   +4 more
doaj   +1 more source

Endoscopic treatment of intussusception due to small intestine polyps in patients with Peutz-Jeghers Syndrome

Endoscopy International Open, 2022
Background and study aims Intussusception caused by intestinal polyps in patients with Peutz-Jeghers syndrome usually requires laparotomy. Patients following successful endoscopic reduction using double-balloon endoscopy (DBE) have been reported. The aim
Kunihiko Oguro, Hirotsugu Sakamoto, Tomonori Yano, Yohei Funayama, Masafumi Kitamura, Manabu Nagayama, Keijiro Sunada, Alan Kawarai Lefor, Hironori Yamamoto   +8 more
doaj   +1 more source

Polyposis: The Peutz-Jeghers syndrome

Journal of British Surgery, 1995
Abstract The classical pigmentation of Peutz-Jeghers syndrome distinguishes it immediately from the other polyposis syndromes. Less widely appreciated than this most obvious manifestation are the pitfalls in management presented by the risk of cancer and by the performance of multiple laparotomies that also characterize this condition ...
A D, Spigelman, P, Arese, R K, Phillips
openaire   +2 more sources