Giant hamartomatous polyp of the uterine cervix with heterologous mesenchymal tissue in a child: a case report [PDF]
Background Polyps of the uterine cervix are one of the most common benign hyperplastic lesions occurring in the female genital tract that usually arise from the endocervical canal and are believed to be the result of reactive changes due to long-standing
Esmatullah Esmat +5 more
doaj +2 more sources
Small intestinal hamartomatous polyp due to Peutz–Jeghers syndrome in middle childhood [PDF]
Small‐bowel surveillance is recommended from the age of 8 years in asymptomatic individuals with Peutz–Jeghers syndrome. Because intussusception and risk of strangulated ileus were noted in an 11‐year‐old patient, small‐bowel surveillance should be ...
Toshihiko Kakiuchi, Takashi Akutagawa
doaj +2 more sources
Adrenocortical Carcinoma in Peutz-Jeghers Syndrome With a Rare STK11 Pathogenic Germline Variant: A Case Report. [PDF]
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 +14 more
europepmc +2 more sources
A Sporadic Juvenile Gastric Polyp: An Endoscopic Rarity. [PDF]
ABSTRACT There are several types of gastric polyps and juvenile gastric polyps are scarce. They can be asymptomatic or can contribute to iron deficiency anemia. Can be sporadic or part of syndromic diagnosis. It's crucial to differentiate from other gastric polyps, as juvenile gastric polyps are rare with clinical implications.
Amin N +3 more
europepmc +2 more sources
Juvenile polyposis in a SMAD4-mutated child: A call for early surveillance. [PDF]
Abstract We report the case of a 10‐year‐old boy with hereditary hemorrhagic telangiectasia (HHT) and a family history of SMAD4‐related juvenile polyposis syndrome (JPS), presenting with hypoferritinaemia unresponsive to oral supplementation. Endoscopic evaluation revealed multiple gastrointestinal polyps, including duodenal, gastric, and colonic ...
Lorusso C +10 more
europepmc +2 more sources
Familial pediatric Peutz–Jeghers syndrome with recurrent intussusception: case report and literature review [PDF]
BackgroundPeutz–Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by mucocutaneous pigmentation and gastrointestinal hamartomatous polyposis, predisposing affected individuals to recurrent small bowel intussusception and ...
Sondes Sahli +17 more
doaj +2 more sources
Solitary Peutz-Jeghers Type Hamartomatous Polyp Arising from the Appendix [PDF]
Mariana Sant’Anna +4 more
doaj +2 more sources
Rare solitary giant hamartomatous polyp of the stomach removed by endoscopic submucosal dissection [PDF]
Dennis Yang, MD +4 more
doaj +2 more sources
A Rare Case of Solitary Peutz Jeghers Type Hamartomatous Duodenal Polyp with Dysplasia! [PDF]
Solitary Peutz Jeghers (SPJ) type hamartomatous polyp is a rare and separate entity from classic Peutz Jeghers syndrome (PJS). A hamartomatous polyp without associated mucocutaneous pigmentations, any other gastrointestinal polyp or a family history of ...
Chetan Devendra Rathi +4 more
doaj +1 more source
A 68‐year‐old female patient was referred to our hospital with a 30‐mm polyp in the second portion of the duodenum found via esophagogastroduodenoscopy. The polyp had an irregular, lobular surface and a thick stalk.
Yasuhiko Hamada +12 more
doaj +1 more source

