Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Crohn's disease most frequently presents in late adolescence or early adulthood and is equally distributed between the genders [1]. Symptoms at presentation vary depending on the location, behaviour and severity of disease, as well as extraintestinal manifestations and medication. The aim is to establish the diagnosis and distribution of disease using appropriate techniques, since this influences the choice of therapy. Originally, Dr. Burrill Crohn and colleagues described regional ileitis as a chronic inflammatory disease restricted to the terminal ileum in association with intestinal stenoses or fistulae, but not crossing the ileocaecal valve [2]. Although Crohn subsequently recognised colonic disease in conjunction with ileitis [3], it was Basil Morson and Lyn Lockhart-Mummery who put colonic Crohn's disease on the diagnostic map [4, 5]. © 2010 Springer-Verlag Berlin Heidelberg.

Original publication

DOI

10.1007/978-3-540-69419-9_30

Type

Chapter

Book title

Anorectal and Colonic Diseases: A Practical Guide to Their Management

Publication Date

01/12/2010

Pages

501 - 511