[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 54.197.75.176. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Article
October 15, 1997

Genetic Testing in Hereditary Colorectal Cancer

Author Affiliations

From the Departments of Medicine and Oncology, The Johns Hopkins Hospital, Baltimore, Md.

JAMA. 1997;278(15):1278-1281. doi:10.1001/jama.1997.03550150082040
Abstract

CASE PRESENTATION  A 29-year-old woman presented to her family physician with a 2-month history of 30 to 44 mL (2-3 tbsp) of bright red blood per rectum with every bowel movement. She was referred to a surgeon, who performed anoscopy and gave her a diagnosis of hemorrhoidal bleeding. She underwent hemorrhoidal surgery of unknown type.The patient again sought medical attention 3 months later, complaining of persistent and unchanged rectal bleeding. She had no change in bowel habits, weight loss, or family history of colorectal cancer or polyps. Examination of her skin did not show osteomas, lipomas, or epidermoid cysts. Direct ophthalmoscopic examination revealed no pigmentation of the retinal epithelium. Abdominal examination was normal. A stool sample taken during rectal examination tested guaiac positive.The results of an upper gastrointestinal tract barium series were normal, but air contrast barium enema showed multiple filling defects throughout the colorectum. Subsequent colonoscopy revealed

×