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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Case Report
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
Descripción
Sumario: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.

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