Results 11 to 20 of about 5,233 (135)
Diagnostic difficulty in Peutz–Jeghers syndrome
Journal of Coloproctology, 2015 A case of diagnostic difficulty facing the patient with colonic polyposis secondary to Peutz–Jeghers syndrome, but without family history and pathognomonic clinical features of the disease, is illustrated.
Jenifer Loureiro +10 more
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PeutzJeghers syndrome: A case report and literature review
Journal of Pathology of Nepal, 2014 Peutz–Jeghers Syndrome is an autosomal dominant inheritedhamartomatous polyp. We present a case of a 5-year-old young boywith a history of per rectal bleeding and mass protruding out of the anus.
A Lakhey, H Shakya
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Cancer problem in Peutz-Jeghers syndrome
Advanced Biomedical Research, 2013 Peutz-Jeghers syndrome is a rare autosomal dominantly inherited condition, characterized by the presence of hamartomatous gastrointestinal polyps and mucocutaneous pigmentation.
Diana Taheri +7 more
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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 +7 more
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Peutz-Jeghers syndrome: A case report
Asian Journal of Medical Sciences, 2021 Peutz-jeghers syndrome is a rare inherited autosomal dominant disease which is characterized by mucocutaneous pigmentation and multiple polyps in the gastrointestinal tract.
Pratima Poudel , Roushan Jahan
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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 +5 more
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Rare cases of Peutz-Jeghers syndrome in children
Сучасна педіатрія: УкраїнаPeutz-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 +3 more
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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 +4 more
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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 +4 more
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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 +5 more
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