Peutz jeghers syndrome - Open Access .click

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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
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Peutz-Jeghers Syndrome

Journal of Cutaneous Medicine and Surgery
Sherman S, Menon G, Krishnamurthy K.
europepmc +4 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, J Thanka, Rajendran Shanmugasundaram +2 more
doaj +1 more source

Peutz-Jeghers syndrome a review of gynecological implications and the management of these patients through the presentation of a case report

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
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The Importance of Simultaneous Surgical and Endoscopic Polypectomies in Peutz-Jeghers Syndrome: A Case Report

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
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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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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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peutz-jeghers syndrome
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intestinal polyps
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