Familial adenomatous polyposis: a case study.

Joseph Yorke,Francis Akwaw Yamoah,Ronald Awoonor-Williams,Thomas Okpoti Konney,Emmanuel Acheampong,Ernest Adjei,Kwabena Acheamfour Ababio, Daniel Gyawu Aning, Dennis Afful-Yorke, Freda Manu Aidoo, Claudia Gyamfua Assim,Frank Enoch Gyamfi, Raphael Owusu Sekyere Assim,Saabea Owusu Konadu, David Elikplim Kuwornu,Emmanuella Nsenbah Acheampong

JOURNAL OF SURGICAL CASE REPORTS(2020)

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摘要
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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关键词
familial adenomatous polyposis,colonoscopy,subtotal colectomy
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