scholarly journals Colonic Interposition in a Woman with Attenuated Familial Adenomatous Polyposis: Does the Location of the Colon Affect Polyp Formation?

2008 ◽  
Vol 22 (7) ◽  
pp. 634-636 ◽  
Author(s):  
Melanie D Beaton ◽  
Brian Taylor ◽  
David Driman ◽  
Peter Ainsworth ◽  
Paul C Adams

Attenuated familial adenomatous polyposis (AFAP) is a rare but well-established cause of colorectal carcinoma and multiple polyps. The present paper describes a case of a woman diagnosed with colorectal cancer at 34 years of age and subsequently found to have AFAP by genetic testing. During infancy, the patient underwent surgical correction of esophageal atresia with colonic interposition. While she had developed adenomatous polyps in her native cecum, there was no evidence of polyps or cancer in the segment of large intestine interposed between her upper esophagus and stomach. Therefore, various environmental differences between the upper and lower gastrointestinal tract may play a role in the expression of AFAP phenotype.

2005 ◽  
Vol 129 (11) ◽  
pp. 1380-1384 ◽  
Author(s):  
Jeremy R. Jass

Abstract Precancerous polyposes other than classic familial adenomatous polyposis and the condition hereditary nonpolyposis colorectal cancer, or Lynch syndrome, continue to present major diagnostic challenges for the anatomic pathologist. This editorial highlights the practical significance of novel insights and clinical guidelines in the recent literature, as well as in 4 contributions to this edition of the Archives of Pathology & Laboratory Medicine. The first section will address attenuated familial adenomatous polyposis and a newly recognized type of autosomal-recessive adenomatous polyposis associated with the DNA repair gene MYH. The remainder of the editorial discusses the role of the revised Bethesda guidelines in the diagnosis of hereditary nonpolyposis colorectal cancer and concludes with the recently identified serrated pathway syndrome.


2018 ◽  
Vol 31 (03) ◽  
pp. 161-167
Author(s):  
Molly Ford

AbstractGrowing knowledge of inherited colorectal cancer syndromes has led to better surveillance and better care of this subset of patients. The most well-known entities, including Lynch syndrome and familial adenomatous polyposis, are continually being studied and with the advent of more sophisticated genetic testing, additional genetic discoveries have been made in the field of inherited cancer. This article will summarize many of the updates to both the familiar and perhaps less familiar syndromes that can lead to inherited or early-onset colorectal cancer.


2004 ◽  
Vol 127 (2) ◽  
pp. 444-451 ◽  
Author(s):  
Randall W. Burt ◽  
Mark F. Leppert ◽  
Martha L. Slattery ◽  
Wade S. Samowitz ◽  
Lisa N. Spirio ◽  
...  

2014 ◽  
Vol 22 (11) ◽  
pp. 1330-1333 ◽  
Author(s):  
Abdulla Ibrahim ◽  
Daniel R Barnes ◽  
Jacqueline Dunlop ◽  
Daniel Barrowdale ◽  
Antonis C Antoniou ◽  
...  

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