نتایج جستجو برای: hamartomatous

تعداد نتایج: 561  

Journal: :Surgical Clinics of North America 2008

Journal: :Cancer 2011
Sherry C Huang Jeffrey K Lee E Julieta Smith Ryan T Doctolero Akihiro Tajima Stayce E Beck Noel Weidner John M Carethers

BACKGROUND Patients with hamartomatous polyposis syndromes have increased risk for colorectal cancer (CRC). Although progression of polyps to carcinoma is observed, pathogenic mechanisms remain unknown. The authors examined whether familial hamartomatous polyps harbor defects in DNA mismatch repair (MMR), and assayed for somatic mutation of PTEN, a gene inactivated in the germline of some hamar...

2006
S. WIDGREN

Patients with the Peutz-Jeghers syndrome carry a slight, though definite, increased risk of gastrointestinal carcinoma.The malignant potentiality of Peutz-Jeghers hamartomatous polyps, generally considered benign, is supported by this report. Two cases of metastasising gastrointestinal carcinoma associated with the Peutz-Jeghers syndrome are described in a 56 year old female and her 29 year old...

2011
Yusuke Sekino Masahiko Inamori Mitsuru Hirai Kaori Suzuki Kaoru Tsuzawa Keiko Akimoto Ayako Takahata Nobutaka Fujisawa Kumiko Saito Akisa Tsunemi Michio Tanaka Hiroshi Iida Yasunari Sakamoto Hirokazu Takahashi Tomoko Koide Chikako Tokoro Yasunobu Abe Atsushi Nakajima Shin Maeda Shigeru Koyama

INTRODUCTION A hamartomatous polyp without associated mucocutaneous pigmentation or a family history of Peutz-Jeghers Syndrome is diagnosed as a solitary Peutz-Jeghers type hamartomatous polyp. As compared with Peutz-Jeghers Syndrome, Peutz-Jeghers type hamartomatous polyps are diagnosed with a lower risk of cancer and are regarded as a different disorder. CASE PRESENTATION In case one, we de...

Journal: :Endoscopy 2013
T Solakoglu E Akin S H O Yavuz O Ersoy

polyp in the intrahepatic biliary duct Hamartomatous polyps are usually found as part of Peutz–Jeghers Syndrome (PJS) and are uncommon, but occasionally a solitary hamartomatous polyp may develop in an otherwise healthy patient [1]. Hamartomatous polyps may appear commonly in the stomach, small bowel, or colon, with hamartomatous features on histology [2,3]. Polyps at extraintestinal sites such...

Journal: :Journal of Korean Medical Science 2000
B. K. Kim Y. I. Kim W. H. Kim

A 42-year-old female diagnosed with tuberous sclerosis was found to have multiple polyps in the fundus of stomach. On histologic examination, the lesions were hamartomatous polyps. In tuberous sclerosis, many lesions occur in multiple organs and there are several reports about the frequent association of hamartomatous polyps of the colon. However, gastric manifestation of tuberous sclerosis has...

2014
Radu Badea Lidia Ciobanu Emil Boţan Cristina Pojoga Marcel Tanţău

The hamartomatous polyps in Peutz-Jeghers syndrome may have malignant potential. To differentiate between hamartomatous and adenomas polyps, vascular characterization can be assessed using noninvasive procedures, such as contrast-enhanced ultrasound (CEUS). The neo-angiogenic characteristics of colorectal adenomas and carcinomas are expressed as an anarchic vascular pattern observed on CEUS. Us...

2015
Christopher M. Flannery John A. Lunn

Cronkhite-Canada syndrome is a rare, hamartomatous polyposis syndrome of unknown etiology. Hamartomatous gastro-intestinal polyps, alopecia, onychodystrophy, cutaneous hyperpigmentation, abdominal pain, diarrhea, and complications of weight loss are typical of the syndrome. In this report, we describe a pathological finding of colonic adenomatous polyposis as opposed to hamartomatous polyposis....

2011
Seung Jong Oh Cheong A Oh Dae Hoon Kim Min Gew Choi Jae Hyung Noh Tae Sung Sohn Kyoung Mee Kim Jae Moon Bae Sung Kim

Most hamartomatous polyps in the stomach occur in patients with adenomatous polyposis coli and dysplasia. The authors report a case of a 57-year-old man without prior history of polyposis coli who presented with adenocarcinomas derived from hamartomatous polyps in the stomach. The patient underwent a radical subtotal gastrectomy with Billroth I anastomosis. Pathology revealed adenocarcinomas wi...

Journal: :Postgraduate medical journal 1990
J C Erdozain J J Sánchez-Ruano A L San Román D Boixeda V F Moreira A G Plaza

A case of solitary gastric hamartomatous polyp, presenting as upper gastrointestinal haemorrhage, is reported. Both the entity itself, and the clinical presentation, are exceptional. The significance of the solitary gastric hamartomatous polyp and implications of its diagnosis are discussed.

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