Hereditary and familial colorectal cancer: Difference between revisions

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==Causes==
==Causes==
==Differentiating type page name here from other Diseases==
== Epidemiology and Demographics ==
===Age===
===Gender===
===Race===
===Developed Countries===
===Developing Countries===
== Risk Factors ==
== Screening ==
== Natural History, Complications and Prognosis==


==[[Hereditary and familial colorectal cancer Diagnosis|Diagnosis]]==
==[[Hereditary and familial colorectal cancer Diagnosis|Diagnosis]]==


== Treatment ==
== Treatment ==
=== Pharmacotherapy ===
==== Acute Pharmacotherapies ====
==== Chronic Pharmacotherapies ====
=== Surgery and Device Based Therapy ===
==== Indications for Surgery ====
==== Pre-Operative Assessment ====
==== Post-Operative Management ====
==== Transplantation ====
=== Primary Prevention ===
=== Secondary Prevention ===
=== Cost-Effectiveness of Therapy ===
=== Future or Investigational Therapies ===


==References==
==References==

Revision as of 10:19, 11 April 2013


For patient information, click Insert page name here

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: colon cancer, inherited syndrome, lynch syndrome, familial adenomatos polyposis, MUTYH-associated polyposis, hamartomatous polyposis,hyperplastic polyposis, common familial colorectal cancers

Overview

Historical Perspective

Classification

Pathophysiology

Associated conditions | Gross Pathology | Microscopic Pathology | Genetics

Causes

Diagnosis

Treatment

References


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