Results 11 to 20 of about 5,184 (174)

Adrenocortical Carcinoma in Peutz-Jeghers Syndrome With a Rare STK11 Pathogenic Germline Variant: A Case Report. [PDF]

Cancer Rep (Hoboken)
ABSTRACT Background Peutz–Jeghers syndrome (PJS) is an inherited, autosomal‐dominant condition, featuring STK11 germline mutations, characterized by hamartomatous gastrointestinal polyps and increased cancer risk. The most commonly associated malignancies are gastrointestinal, pancreatic, and breast cancers.
Ishida T, Kandori S, Takahashi R, Nitta S, Shiga M, Nagumo Y, Kawahara T, Hoshi A, Negoro H, Mathis BJ, Sugita S, Matsubara D, Ishiguro T, Nakajima T, Nishiyama H.   +14 more
europepmc   +2 more sources

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

A rare case of gastric-type mucinous adenocarcinoma in a woman with Peutz-Jeghers syndrome [PDF]

Obstetrics & Gynecology Science, 2019
Adenocarcinoma of the cervix is less common than squamous cell carcinoma. Minimal deviation adenocarcinoma (adenoma malignum) is considered an extremely well-differentiated variant of GAS.
Yeorae Kim, Eun Yi Kim, Tae Jin Kim, Kyung Taek Lim, Ki Heon Lee, Yikyeong Chun, Kyeong A So   +6 more
doaj   +1 more source

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, Grażyna Jarząbek-Bielecka, Piotr Merks, Katarzyna Wróblewska-Seniuk, Małgorzata Mizgier, Ewa Jakubek, Samuel Grześkiewicz, Małgorzata Wójcik, Witold Kędzia   +8 more
doaj   +1 more source

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, Tunç Eren, Aman Gapbarov, Hatice Şeneldir, İbrahim Ali Özemir, Özgür Ekinci, Orhan Alimoğlu   +6 more
doaj   +1 more source

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, Gian Luigi Menegazzo, Lucas Vergamini, Roberto Carmagnani Pestana, Fernanda Bellotti Formiga, Marcella Guilherme Carolino de Sousa, Thais Yuka Takahashi, Felipe Silveira, Paulo de Azeredo Passos Candelária, Dino Martini Filho, Fang Chia Bin   +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
doaj   +1 more source

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, Noushin Afshar-Moghadam, Parvin Mahzoni, Amin Eftekhari, Seyed Mozafar Hashemi, Mohammad Hasan Emami, Mehdi Fesharakizadeh, Hamid Reza Ghasemi-basir   +7 more
doaj   +1 more source

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
doaj   +1 more source