Cargando…
Familial adenomatous polyposis: a case study
Familial adenomatous polyposis (FAP) is an inherited syndrome characterized by several adenomatous polyps of the gastrointestinal (GI) mucosa. If treatment is not provided, an average individual with classic FAP will develop colorectal carcinoma around the age of 40 years. The incidence rate of FAP...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588306/ https://www.ncbi.nlm.nih.gov/pubmed/33133502 http://dx.doi.org/10.1093/jscr/rjaa367 |
_version_ | 1783600343616061440 |
---|---|
author | Yorke, Joseph Yamoah, Francis Akwaw Awoonor-Williams, Ronald Konney, Thomas Okpoti Acheampong, Emmanuel Adjei, Ernest Ababio, Kwabena Acheamfour Aning, Daniel Gyawu Afful-Yorke, Dennis Aidoo, Freda Manu Assim, Claudia Gyamfua Gyamfi, Frank Enoch Assim, Raphael Owusu Sekyere Konadu, Saabea Owusu Kuwornu, David Elikplim Acheampong, Emmanuella Nsenbah |
author_facet | Yorke, Joseph Yamoah, Francis Akwaw Awoonor-Williams, Ronald Konney, Thomas Okpoti Acheampong, Emmanuel Adjei, Ernest Ababio, Kwabena Acheamfour Aning, Daniel Gyawu Afful-Yorke, Dennis Aidoo, Freda Manu Assim, Claudia Gyamfua Gyamfi, Frank Enoch Assim, Raphael Owusu Sekyere Konadu, Saabea Owusu Kuwornu, David Elikplim Acheampong, Emmanuella Nsenbah |
author_sort | Yorke, Joseph |
collection | PubMed |
description | Familial adenomatous polyposis (FAP) is an inherited syndrome characterized by several adenomatous polyps of the gastrointestinal (GI) mucosa. If treatment is not provided, an average individual with classic FAP will develop colorectal carcinoma around the age of 40 years. The incidence rate of FAP in developing countries like Ghana is unknown compared to advanced countries. We present the first FAP case of a 22-year-old Ghanaian female who presented with massive lower GI bleeding and underwent surgical management after a thorough investigation. The initial assumption that colonic polyps are scarce in native Africans may be more than what is perceived. This highlights the need for the availability of endoscopic services in Ghana. |
format | Online Article Text |
id | pubmed-7588306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-75883062020-10-30 Familial adenomatous polyposis: a case study Yorke, Joseph Yamoah, Francis Akwaw Awoonor-Williams, Ronald Konney, Thomas Okpoti Acheampong, Emmanuel Adjei, Ernest Ababio, Kwabena Acheamfour Aning, Daniel Gyawu Afful-Yorke, Dennis Aidoo, Freda Manu Assim, Claudia Gyamfua Gyamfi, Frank Enoch Assim, Raphael Owusu Sekyere Konadu, Saabea Owusu Kuwornu, David Elikplim Acheampong, Emmanuella Nsenbah J Surg Case Rep Case Report Familial adenomatous polyposis (FAP) is an inherited syndrome characterized by several adenomatous polyps of the gastrointestinal (GI) mucosa. If treatment is not provided, an average individual with classic FAP will develop colorectal carcinoma around the age of 40 years. The incidence rate of FAP in developing countries like Ghana is unknown compared to advanced countries. We present the first FAP case of a 22-year-old Ghanaian female who presented with massive lower GI bleeding and underwent surgical management after a thorough investigation. The initial assumption that colonic polyps are scarce in native Africans may be more than what is perceived. This highlights the need for the availability of endoscopic services in Ghana. Oxford University Press 2020-10-27 /pmc/articles/PMC7588306/ /pubmed/33133502 http://dx.doi.org/10.1093/jscr/rjaa367 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2020. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Case Report Yorke, Joseph Yamoah, Francis Akwaw Awoonor-Williams, Ronald Konney, Thomas Okpoti Acheampong, Emmanuel Adjei, Ernest Ababio, Kwabena Acheamfour Aning, Daniel Gyawu Afful-Yorke, Dennis Aidoo, Freda Manu Assim, Claudia Gyamfua Gyamfi, Frank Enoch Assim, Raphael Owusu Sekyere Konadu, Saabea Owusu Kuwornu, David Elikplim Acheampong, Emmanuella Nsenbah Familial adenomatous polyposis: a case study |
title | Familial adenomatous polyposis: a case study |
title_full | Familial adenomatous polyposis: a case study |
title_fullStr | Familial adenomatous polyposis: a case study |
title_full_unstemmed | Familial adenomatous polyposis: a case study |
title_short | Familial adenomatous polyposis: a case study |
title_sort | familial adenomatous polyposis: a case study |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588306/ https://www.ncbi.nlm.nih.gov/pubmed/33133502 http://dx.doi.org/10.1093/jscr/rjaa367 |
work_keys_str_mv | AT yorkejoseph familialadenomatouspolyposisacasestudy AT yamoahfrancisakwaw familialadenomatouspolyposisacasestudy AT awoonorwilliamsronald familialadenomatouspolyposisacasestudy AT konneythomasokpoti familialadenomatouspolyposisacasestudy AT acheampongemmanuel familialadenomatouspolyposisacasestudy AT adjeiernest familialadenomatouspolyposisacasestudy AT ababiokwabenaacheamfour familialadenomatouspolyposisacasestudy AT aningdanielgyawu familialadenomatouspolyposisacasestudy AT affulyorkedennis familialadenomatouspolyposisacasestudy AT aidoofredamanu familialadenomatouspolyposisacasestudy AT assimclaudiagyamfua familialadenomatouspolyposisacasestudy AT gyamfifrankenoch familialadenomatouspolyposisacasestudy AT assimraphaelowususekyere familialadenomatouspolyposisacasestudy AT konadusaabeaowusu familialadenomatouspolyposisacasestudy AT kuwornudavidelikplim familialadenomatouspolyposisacasestudy AT acheampongemmanuellansenbah familialadenomatouspolyposisacasestudy |