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Relevant bibliographies by topics / Hamartomatous Polyps

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Academic literature on the topic 'Hamartomatous Polyps'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "Hamartomatous Polyps"

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Hilmi, Mohammed Natiq. "The Prevalence and Histopathological Types of Colonic Polyps Removed during Colonoscopy in Tertiary Hospital Center: A four-year Retrospective Study." Iraqi Journal of Community Medicine 38, no. 2 (2025): 123–28. https://doi.org/10.4103/irjcm.irjcm_44_24.

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Abstract Background: Colonic polyps can be classified endoscopically as sessile (flat lesion) and pedunculated (a lesion with a stalk); however, the most important classification for treatment and prognosis is the histopathological one which divides polyps into adenomatous, serrated, juvenile/retention, inflammatory, mucosal, and hamartomatous polyps. Objective: The aim of this study is to detect the prevalence and types of colonic polyps removed during colonoscopic examination with their clinicopathological characteristics. Methods: A cross-sectional retrospective study was performed to analy

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Elkholy, Shimaa S., Shaymaa S. El Gammal, Marwa S. Rizk, Sally W. Elkhadry, Heba M. Abdallah, and Salma A. M. Nagi. "Clinicopathological findings in relation to beclin-1 protein expression among patients with Juvenile/Hamartomatous Polyps." Egyptian Journal of Pathology 44, no. 2 (2024): 167–74. https://doi.org/10.4103/egjp.egjp_28_24.

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Background Juvenile or hamartomatous polyps represent the most common pediatric polyps. Although neoplastic transformation in juvenile polyps is uncommon, dysplastic alterations were observed. The role of autophagy in hamartomatous lesions remains unclear. Objectives To assess the relationship between clinicopathological changes and beclin-1 protein expression among patients with juvenile/hamartomatous polyps. Patients and methods A total of 134 patients were enrolled in a case–control study: 63 cases of juvenile polyps, 59 colonic tissues as controls, and 12 colonic adenomas. All colonic tiss

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Vyas, Monika, Xiu Yang, and Xuchen Zhang. "Gastric Hamartomatous Polyps—Review and Update." Clinical Medicine Insights: Gastroenterology 9 (January 2016): CGast.S38452. http://dx.doi.org/10.4137/cgast.s38452.

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Gastric polyps are frequently encountered on endoscopic examinations. While many of these represent true epithelial lesions, some of the polyps may result from underlying stromal or lymphoid proliferations or even heterotopic tissue. Histologic examination is essential for accurate typing of the polyps to predict malignant potential and underlying possible genetic abnormalities. The focus of this review is on gastric hamartomatous polyps, which are relatively rare and diagnostically challenging. Though most of the gastric hamartomatous polyps are benign, certain types are associated with incre

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Tim, Lee Mem, Wan Zain Wan Zainira, and Othman Faeid. "Double Intussusceptions in Peutz-Jeghers Syndrome Patient: A Case Report." Ethiopian Medical Journal 62, no. 1 (2024): 69–72. http://dx.doi.org/10.4314/emj.v62i1.10.

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Background: Peutz-Jeghers Syndrome is one of the hereditary gastro-intestinal cancer syndrome with characteristic mucocutaneous pigmentation and histologically distinctive hamartomatous polyps in gastro-intestinal tract. Although it is characteristically benign hamartomatous polyp, majority of affected individuals develop symptoms starting from their second decades. We reported a known Peutz-Jeghers Syndrome case developed recurrent polyps leading to double intussusceptions required bowel resection. Multidisciplinary management and patient compliance to surveillance regime are important in man

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Chiu, Kenrry, Lik Hang Lee, and Wei Xiong. "Gastric Polyposis Syndromes." AJSP: Reviews and Reports 24, no. 4 (2019): 133–43. http://dx.doi.org/10.1097/pcr.0000000000000311.

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Abstract Most gastric polyps are fundic gland polyps and hyperplastic polyps. Adenomas, inflammatory fibroid polyps, and neuroendocrine tumors are other types of gastric polyps that occur less frequently. Rarely, a gastric polyp may be associated with a syndrome, including hereditary cancer syndromes. Some of these syndromes are also associated with an increased risk of gastric cancer. We present a case of a 50-year-old woman with known Cowden syndrome who presents with multiple gastric hamartomatous polyps. We then review the clinical, endoscopic, and pathologic features of various syndromes

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Venkatesh, Kusuma, Karishma Pillarisetty, and Sreedhara Murthy B. N. "Juvenile polyposis syndrome with extraintestinal anomalies: report of a rare case with review of literature." International Journal of Research in Medical Sciences 5, no. 2 (2017): 720. http://dx.doi.org/10.18203/2320-6012.ijrms20170183.

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Juvenile polyposis coli is a rare condition in children with neoplastic potential having an incidence of about 1 in 1,00,000 population. A minority of such patients have extraintestinal abnormalities like cardiac and pulmonary arteriovenous malformations. Juvenile polyposis is a disorder of hamartomatous polyposis syndrome having a malignant potential. The progression of hamartomatous polyp to carcinoma is still elucidated when compared to the understanding of transformation of an adenomatous polyp into a carcinoma via a gatekeeper defect. Here is the report of a rare case of Juvenile polyposi

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Athar, Z., A. Rajbhandari, P. Kansakar, Y. P. Singh, and P. Vaidya. "Peutz-Jehger’s Syndrome presenting as adult intussusception." Journal of Institute of Medicine Nepal 31, no. 1 (2009): 30–32. http://dx.doi.org/10.59779/jiomnepal.374.

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Abstract: Peutz- Jehger’s syndrome is an autosomal dominant disorder. It is the second most common hamartomatous syndrome with hamartomatous polyp of gastrointestinal tract and cutaneous melanin deposit. Majority of patients remain relatively asymptomatic. Some present with abdominal pain secondary to obstruction or impending obstruction owing to an intussuscepted polyp with GI bleeding. We report a case of 21 year male who presented with upper central abdominal pain, distension, vomiting and blood mixed stool. He also had black colored spots on perioral region and fingers. Ultrasound revealed

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Cone, Molly. "Hamartomatous Polyps and Associated Syndromes." Clinics in Colon and Rectal Surgery 29, no. 04 (2016): 330–35. http://dx.doi.org/10.1055/s-0036-1582441.

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AbstractHamartomatous polyps of the gastrointestinal tract can occur sporadically, however, for several hereditary syndromes, their presence is one of the major clinical features. Peutz–Jeghers syndrome, juvenile polyposis syndrome, and the PTEN hamartoma syndromes are autosomal dominant inherited disorders that predispose to formation of such polyps, especially in the colon and rectum. These can lead to increased colorectal cancer risk and should be followed and managed appropriately. In this article, the three major hereditary hamartomatous syndromes are described, including presentation, co

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Soni, Sarita, Saurabh Sharma, K. Bhindiya, Aditya Jamwal, and Rashmi Kaul. "Histopathological Analysis of Gastrointestinal Polyps: A Yearlong Study at a Tertiary Care Center." International Journal of Medical and Biomedical Studies 8, no. 3 (2024): 132–35. http://dx.doi.org/10.32553/ijmbs.v8i3.2827.

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This retrospective study was conducted at a tertiary care institute from January to December 2023. The study aimed to evaluate the range of histological characteristics seen in gastrointestinal polyps. By employing Hematoxylin and Eosin (H&E) stained slides, a total of 62 cases were examined in order to categorise polyps according to age, gender, location, and histological type. The results indicated that adenomatous polyps were primarily located in the large intestine, while hyperplastic polyps were more prevalent in the stomach. Additional forms that were detected include hamartomatous,

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Chaudhary, Gyanendra, Sachin Agrawal, Situ Situ, and Ananvay Dadu. "Peutz-Jeghers Syndrome Causing Gastroduodenal Intussusception : A Rare Case Report." Journal of Nepal Paediatric Society 43, no. 1 (2023): 108–10. http://dx.doi.org/10.60086/jnps499.

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Peutz-Jeghers syndrome (PJS) is a rare disease characterized by melanotic macular lesions over the pulp of fingers, in oral cavity mucosa, lips, and hamartomatous gastric and intestinal polyps. They usually present with intestinal intussusception or intestinal bleeding; gastroduodenal intussusception is an infrequent presentation. Endoscopic resection or complete surgical excision of the polyp is the treatment of choice. We here present a case of a seven year male with multiple gastric polyps presenting as gastric outlet obstruction.

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Book chapters on the topic "Hamartomatous Polyps"

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Baldaia, Helena. "Hamartomatous Polyps." In Encyclopedia of Pathology. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-40560-5_1629.

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Ambe, Peter C., and Gabriela Möslein. "Management of Hamartomatous Polyps." In Management of Hereditary Colorectal Cancer. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-26234-1_2.

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Namikawa, Ken, and Toshiaki Hirasawa. "Gastric Polyp: Inflammatory Fibroid Polyp, Hyperplastic Polyp, and Inverted Hamartomatous Polyp." In Endoscopic Treatment Strategy for Upper GI Tract Neoplasms. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-32-9737-1_6.

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"Hamartomatous Polyps." In Encyclopedia of Cancer. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-16483-5_6534.

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"Hamartomatous Polyps, Juvenile." In Diagnostic Pathology: Gastrointestinal. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-37673-0.50169-5.

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"Hamartomatous Polyps, Cowden Syndrome." In Diagnostic Pathology: Gastrointestinal. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-37673-0.50167-1.

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"Hamartomatous Polyps, Cronkhite-Canada." In Diagnostic Pathology: Gastrointestinal. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-37673-0.50168-3.

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"Hamartomatous Polyps, Peutz-Jeghers." In Diagnostic Pathology: Gastrointestinal. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-37673-0.50170-1.

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Sheridan, E., and R. S. Houlston. "Management of familial adenomatous polyposis and other inherited polyposis syndromes." In Risk Assessment and Management in Cancer Genetics. Oxford University PressOxford, 2005. http://dx.doi.org/10.1093/oso/9780198529606.003.0010.

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Abstract Colorectal polyps can be grouped according to their histology. The most important subgroups are adenomatous polyps and hamartomatous polyps. Adenomatous polyps account for around 30 to 50 per cent of all polyps and are premalignant lesions. They are detectable in around 15 to 20 per cent of the population by age 50, the risk increasing with age (Fig. 9.1). Autopsy series suggest that the incidence is even higher, with 60 per cent of men having a polyp by age 50 compared with only 40 per cent of women.

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"Hamartomatous Polyps, Heterotopias, Unclassified Polyps, and Tumor-Like Lesions." In Tumors of the Intestines. American Registry of PathologyWashington, DC, 2017. http://dx.doi.org/10.55418/9781933477398-02.

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Conference papers on the topic "Hamartomatous Polyps"

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Dasgupta, R., J. L. Myers, E. Hussein, et al. "Hamartomatous Endobronchial Polyp: A Unique Cause of Endobronchial Obstruction in a Smoker." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a2335.

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