Results 31 to 40 of about 4,831 (162)
The course and clinical manifestations of Peutz–Jeghers syndrome in the Russian population [PDF]
Терапевтический архив, 2023 Background. PeutzJeghers syndrome (PJS) is a rare hereditary syndrome characterized by the growth of hamartomatous polyps in the gastrointestinal tract, perioral pigmentation and an increased risk of malignant neoplasms.
Тatyana A. Savelyeva +10 more
doaj +1 more source
Peutz-Jeghers syndrome: A circumventable emergency
Indian Journal of Dermatology, 2018 Peutz-Jeghers syndrome (PJS) is characterized by multiple hamartomatous polyps in the gastrointestinal tract and mucocutaneous pigmentation. Here we present, a case of multiple gastrointestinal hamartomatous polyps in a 22-year-old male who had been ...
Sourav Choudhury +4 more
doaj +1 more source
Juvenile polyposis syndrome: A case report
Clinical Case Reports, 2023 Juvenile polyposis syndrome (JPS) is an autosomal dominant disease that is characterized by multiple hamartomatous polyps. Patients with JPS are at increased risk for developing colorectal and gastric cancer. JPS was diagnosed by endoscopy and histology,
Edwin Mogere +6 more
doaj +1 more source
Nowotwory, 2022 Hamartomatous polyp syndromes are a clinically and genetically heterogenous group of rare disorders that fall into the category of inherited predisposition to cancer.
Tomasz Pytrus +4 more
doaj +1 more source
Peutz–Jeghers Syndrome which Develops into Descending Sigmoid Colon Adenocarcinoma
Indonesian Journal of Cancer, 2022 Introduction: Peutz–Jeghers Syndrome (PJS) is an autosomal dominant hereditary condition mainly characterized by hamartomatous gastrointestinal (GI) polyps. Medical treatment is often sought due to complications that arise from the polyps.
Abdul Mughni +2 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
Juvenile Polyposis Syndrome in 11- Years Old Girl [PDF]
Afro-Egyptian Journal of Infectious and Endemic Diseases, 2014 A 11-years old Egyptian girl presented by bleeding per rectum. On endoscopic examination, multiple sigmoid colon polyps(>5) with mucosal prolapse were seen. Polypectomy was done in multiple sessions ( this video shows the first session) .
Tarik Zaher
doaj +1 more source
DEN Open, Volume 7, Issue 1, April 2027.ABSTRACT Uterine leiomyosarcoma (uLMS) is a rare, aggressive uterine malignancy that usually metastasizes hematogenously, whereas gastrointestinal involvement is uncommon. A 69‐year‐old woman with uLMS treated by hysterectomy and adjuvant chemotherapy developed metachronous lung, sigmoid colon, gallbladder, and abdominal wall metastases.
Yuiko Nagasawa +9 more
wiley +1 more source
Clinical and Radiological Features of Cronkhite–Canada Syndrome: A Case Report
Journal of Gastrointestinal and Abdominal Radiology, 2022 Cronkhite–Canada syndrome is a rare non-hereditary disease characterized by gastrointestinal hamartomatous polyposis and protein-losing enteropathy.
Lokesh Lokesh +5 more
doaj +1 more source
The Journal of Pathology, Volume 270, Issue 1, Page 4-22, September 2026.Abstract Gastrointestinal cancer is a global health problem. In the new 6th edition of the World Health Organization Classification of Tumours (WCT) of the Digestive System, updated evidence and guidance is provided for the aetiology, pathogenesis, diagnosis, classification, grading, staging and prognosis of these tumours.
Iris D Nagtegaal +5 more
wiley +1 more source