Results 11 to 20 of about 10,344 (216)

Ovarian Sex Cord Stromal Tumor With Annular Tubules: A Rare Diagnosis in Young Women

Clinical Case Reports
Ovarian sex cord‐stromal tumor with annular tubules (SCTAT) is a rare neoplasm with distinct clinicopathological features in its sporadic and syndromic forms, the latter commonly associated with Peutz‐Jeghers syndrome.
Prescillia Marques, Thiago Vieira, Raquel Brodbeck Ilgenfritz, Dusan Djokovic   +3 more
doaj   +2 more sources

Peutz-Jeghers syndrome: revisited

Autopsy and Case Reports, 2022
Vitorino Modesto dos Santos, Lister Arruda Modesto dos Santos, Laura Campos Modesto   +2 more
doaj   +4 more sources

Peutz-Jeghers syndrome

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, Syed, Abdul Wahid, Yatoo, Ghulam Nabi, Zargar, Showkat Ali, Malik, Rayees Ahmad   +4 more
openaire   +4 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

Peutz–Jeghers syndrome revealed by recurrent small bowel intussusceptions in children: A case report

Clinical Case Reports, 2022
Peutz–Jeghers syndrome is a rare but potentially life‐threating syndrome. We report here the case of a young girl who presented recurrent small bowel intussusceptions.
Chtourou Rahma, Ben Kraiem Najoua, Zouari Mohamed, Mellouli Manel, Dghaies Rim, Ben Dhaou Mahdi, Sellami Boudawara Tahya, Mhiri Riadh   +7 more
doaj   +1 more source

Peutz-Jeghers syndrome [PDF]

Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2018
non ...
Radio C, Grammatico P
openaire   +3 more sources

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

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

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

Peutz-Jeghers syndrome and duodeno-jejunal adenocarcinoma-therapeutic implications [PDF]

, 2009
The Peutz-Jeghers syndrome (PJS) is an autosomal dominant hamartomatous poliposis describred in 1921. Hemminki in 1997 described the presence of LKB-1 mutation tumor-suppressor gen.The patients with PJS develop a higher cumulative incidence of ...
Angós, R. (Ramón), Baixauli, J. (Jorge), Blasco-Blanco, M. (Manuel), Bueno, A. (Álvaro), Hernandez-Lizoain, J.L. (Jose Luis), Idoate, M.A. (Miguel Ángel), Martinez-Regueira, F. (Fernando), Zozaya, G. (Gabriel), Álvarez-Cienfuegos, J. (Javier)   +8 more
core   +1 more source