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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/29698
Title: FAMILIAL ADENOMATOUS POLYPOSIS (FAP) IN CHILDREN: CLINICAL PRESENTATION, GENETIC BASIS, AND MANAGEMENT STRATEGIES
Authors: Pratikshya Holkar
Keywords: Familial adenomatous polyposis;FAP;children;pediatric;genetic testing;APC gene;colonoscopy;colectomy;colorectal cancer;early diagnosis
Issue Date: 2024
Publisher: Instituţia Publică Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu” din Republica Moldova
Citation: Pratikshya Holkar. FAMILIAL ADENOMATOUS POLYPOSIS (FAP) IN CHILDREN: CLINICAL PRESENTATION, GENETIC BASIS, AND MANAGEMENT STRATEGIES. In: Revista de Ştiinţe ale Sănătăţii din Moldova = Moldovan Journal of Health Sciences. 2024, vol. 11, Nr. 3, anexa 2, p. 697. ISSN 2345-1467.
Abstract: Background. Familial adenomatous polyposis (FAP) is a hereditary disorder characterized by the formation of numerous adenomatous polyps in the colon and rectum, lead ing to a high risk of colorectal cancer if untreated. Objective of the study. The aim of this study was to explore the clinical presentation, genetic basis, diagnostic approaches, and management strategies for FAP in the pediatric population. Material and methods. A comprehensive literature review was conducted related to pediatric FAP from 2000 to 2023. Studies involving children (ages 0-18) diagnosed with FAP were included, while studies not distinguishing between pediatric and adult populations, focusing solely on sporadic polyposis, or lacking original data were excluded. Results. Although FAP primarily affects adults, its early onset in chil dren poses unique diagnostic and management challenges. The prevalence of FAP in children was found to be between FAMILIAL ADENOMATOUS POLYPOSIS (FAP) IN CHILDREN: CLINICAL PRESENTATION, GENETIC BASIS, AND MANAGEMENT STRATEGIES Pratikshya Holkar 1 Scientific adviser: Alina Dănilă1,2 1 Natalia Gheorghiu Pediatric Surgery, Orthopedics and Anesthesiology Department, Nicolae Testemițanu University 2 Institute of Mother and Child 1 in 8,000 and 1 in 10,000. Common clinical manifestations included rectal bleeding, abdominal pain, and diarrhea, with polyp detection typically occurring around the age of 15. Genetic testing for APC gene mutations was essential for early diagnosis. Endoscopic surveillance, for at-risk individ uals, was crucial. Prophylactic colectomy was identified as the definitive treatment to prevent colorectal cancer, which posed a near-100% risk by the fourth decade if untreated. Conclusion. Early identification of FAP in children through genetic screening enabled timely surveillance and intervention, significantly reducing morbidity and mortality. Ad vances in genetic therapies and chemoprevention were sug gested as promising areas for future research.
metadata.dc.relation.ispartof: Revista de Științe ale Sănătății din Moldova = Moldovan Journal of Health Sciences
URI: https://cercetare.usmf.md/sites/default/files/inline-files/MJHS_11_3_2024_anexa2__site.pdf
http://repository.usmf.md/handle/20.500.12710/29698
ISSN: 2345-1467
Appears in Collections:Revista de Științe ale Sănătății din Moldova : Moldovan Journal of Health Sciences 2024 Vol. 11, Issue 2

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