Hereditary nonpolyposis colorectal cancer differential diagnosis: Difference between revisions
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juvenile polyposis, familial adenomatous polyposis (FAP), Cowden syndrome and MYH-associated polyposis.<ref> Kladny J, Lubinski J. Lynch syndrome (HNPCC). Hered Cancer Clin Pract. 2008;6(2):99-102.</ref> | juvenile polyposis, familial adenomatous polyposis (FAP), Cowden syndrome and MYH-associated polyposis.<ref> Kladny J, Lubinski J. Lynch syndrome (HNPCC). Hered Cancer Clin Pract. 2008;6(2):99-102.</ref> | ||
== | ==Differentiating Hereditary Nonpolyposis Colorectal Cancer from other Diseases== | ||
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Revision as of 20:15, 8 January 2016
Hereditary Nonpolyposis Colorectal Cancer Microchapters |
Differentiating Hereditary Nonpolyposis Colorectal Cancer from other Diseases |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Maria Fernanda Villarreal, M.D. [2]
Overview
Hereditary nonpolyposis colorectal cancer must be differentiated from other diseases that cause familial colorectal cancer, such as juvenile polyposis, familial adenomatous polyposis (FAP), Cowden syndrome and MYH-associated polyposis.[1]
Differentiating Hereditary Nonpolyposis Colorectal Cancer from other Diseases
Differential Diagnosis | Similar Features | Differentiating Features |
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Familial adenomatous polyposis |
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Juvenile polyposis |
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Cowden syndrome |
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References
- ↑ Kladny J, Lubinski J. Lynch syndrome (HNPCC). Hered Cancer Clin Pract. 2008;6(2):99-102.