Results 21 to 30 of about 5,377 (175)
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 +4 more
openaire +4 more sources
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
High Grade Dysplastic Villous Adenoma Arising from a Giant Hamartomatous Polyp- A Rare Case Presentation [PDF]
Journal of Clinical and Diagnostic Research, 2022 Adenomatous polyps can be found throughout the colon, most commonly in right colon. Microscopically they are classified as tubular, villous or tubulovillous subtypes.
Sayan Bhowmik +2 more
doaj +1 more source
Clinical and Experimental Obstetrics & Gynecology, 2022 Background: Peutz-Jeghers Syndrome (PJS) is a rare autosomal dominant genetic condition caused by mutations in STK11 (Serine/threonine kinase 11) gene (OMIM 602216 Serine/Threonine Protein Kinase 11) located in the short arm of chromosome 19 (19p.13.3 ...
Katarzyna Plagens-Rotman +8 more
doaj +1 more source
İstanbul Medical Journal, 2020 Peutz-Jeghers syndrome may be presented with gastrointestinal and extra-intestinal malignancies. Herein, we report a case of Peutz-Jeghers syndrome with a malignant intestinal polyp accompanied by synchronous multiple hamartomatous gastrointestinal ...
Damla Beyazadam +6 more
doaj +1 more source
Peutz-Jeghers syndrome: revisited
Autopsy and Case Reports, 2022 Vitorino Modesto dos Santos +2 more
doaj +4 more sources
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
doaj +1 more source
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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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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