Adenocarcinoma of the appendix
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Adenocarcinoma of the appendix is a epithelial cancer of the appendix.[2] The term 'epithelium' refers to cells that line hollow organs and glands and those that make up the outer surface of the body. Epithelial cells help to protect or enclose organs. Some produce mucus or other secretions.[1] Types of adenocarcinoma of the appendix include mucinous adenocarcinoma, non-mucinous adenocarcinoma, and possibly signet cell carcinoma of appendix (this is still debated).[2][3]
References
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Epithelium. MedlinePlus. 2006 Available at: http://www.nlm.nih.gov/medlineplus/ency/article/002363.htm. Accessed August 6, 2008.
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Sarosi GA, Turnage RH.. Sleisenger & Fordtran's Gastrointestinal and Liver Disease. 8th ed. In: . Miscellaneous topics. Philadelphia, PA:Saunders; 2006:
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Ahmed K, Hoque R, El-Tawil S, Khan MS, George ML. Adenocarcinoma of the appendix presenting as bilateral ureteric obstruction. World J Surg Oncol. 2008 Feb 21.
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Adenocarcinoma of the appendix
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General | Selected Full-Text Journal Articles
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More Detailed Information (Found 3 resources)
Links where you can find more general information, comprehensive resources, selected full text journal articles, and news updates. Disclaimer
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General
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Cancer.Net, oncologist-approved cancer information from the American Society of Clinical Oncology, has information about appendix cancer. Click on the link to view the information.
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PubMed is a searchable database of medical literature and lists journal articles that discuss Adenocarcinoma of the appendix. Click on the link to view a sample search on this topic.
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Selected Full-Text Journal Articles
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O'Donnell ME, Carson J, Garstin WIH. Surgical Treatment of Malignant Carcinoid Tumours of the Appendix. Int J Clin Pract. 2007;61(3):431-437
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Organizations Providing General Support | Social Networking Websites
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Organizations (Found 10 resources)
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Rare Cancer Alliance
1649 North Pacana Way Green Valley, AZ 85614 Telephone: 520-625-5495 Web site: http://www.rare-cancer.org
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Cancer.net
Toll-free: 888-651-3038 Phone: 571-483-1780 Fax: 571-366-9537 E-mail: contactus@cancer.net Web site: http://www.cancer.net/
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Cancer Hope Network
2 North Road, Suite A Chester, NJ 07930 Toll-free: 1-800-552-4366 Telephone: 908-879-4039 Fax: 908-879-6518 E-mail: info@cancerhopenetwork.org/ Web site: http://www.cancerhopenetwork.org/
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American Cancer Society
1599 Clifton Road NE Atlanta GA 30329 Toll-free: 1-800-227-2345 E-mail: http://www.cancer.org/asp/contactUs/cus_global.asp Web site: http://www.cancer.org
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Cancer Coalition of America
9396 Richmond Ave #307 Houston, TX 77063 Telephone: 832-5268427 E-mail: evainhouston@yahoo.com/ Web site: http://www.cancercoalition.com
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Organizations Providing General Support
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Genetic Alliance
4301 Connecticut Avenue NW Suite 404 Washington, DC 20008-2369 Telephone: 202-966-5557 Fax: 202-966-8553 E-mail: info@geneticalliance.org Web site: http://www.geneticalliance.org
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National Organization for Rare Disorders (NORD)
55 Kenosia Avenue PO Box 1968 Danbury, CT 06813-1968 Toll-free: 1-800-999-6673 (voicemail only) Telephone: 203-744-0100 TTY: 203-797-9590 Fax: 203-798-2291 E-mail: orphan@rarediseases.org Web site: http://www.rarediseases.org/
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Social Networking Websites
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DNAandU.org is a Web site and blog that collects firsthand stories from people facing issues, making tough decisions, and using genomic (DNA) information in their own healthcare. Click on the link to learn from their experiences and/or submit your own story.
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Madisons Foundation
P.O. Box 241956 Los Angeles, CA 90024 Telephone: 310-264-0826 Fax: 310-264-4766 E-mail: getinfo@madisonsfoundation.org Web site: http://www.madisonsfoundation.org/
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RareShare is an online social hub dedicated to patients, families and healthcare professionals affected by rare medical disorders.
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Services (Found 2 resources)
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Many individuals want to know about healthcare professionals or researchers who have knowledge of their conditions. When a condition is rare, it can be difficult to find someone who has seen many cases. Although there is no list of experts in rare diseases, GARD's How to Find an Expert fact sheet provides several ways to identify healthcare professionals who have experience with a particular condition. Click on the link to access this resource and learn more.
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Parent Resources
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The Parent Technical Assistance Center Network provides a list of the Parent Training and Information Centers in each state. These centers are funded by the United States Department of Education to provide early intervention and special education information and training to parents of children with disabilities from birth to age 26. Click on the link to find the Parent Center in your state.
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Scientific Conferences (Found 4 resources)
Resources where you can find information on completed and upcoming scientific conferences and programs. Disclaimer
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Past Conferences
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RDCRN 3rd Conference on Clinical Research for Rare Diseases, October 2, 2012
Location: Hilton Washington DC/Rockville Hotel & Executive Meeting Center, Rockville, MD Description: Clinical research in rare diseases presents a number of challenges and unique issues that are not usually considered in the training of clinical investigators through existing training programs. Goals of the conference include: direct instruction of trainees and new investigators in rare disease research methodology; development of a reusable curriculum/syllabus on rare disease research methodology; and stimulation of ideas regarding the unique issues facing investigators engaged in the study of rare diseases.
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5th International Conference on Epithelial Mesenchymal Transition, October 10, 2011 - October 13, 2011
Description: The objectives of the meeting are to 1) Bring together investigators in the separate disciplines of cancer, pathology and development to discuss their observations on EMT and explore whether there is a consensus on important components of the process. 2) Provide a forum where students and junior investigators can interact with senior investigators and display their own work and ideas in the field. 3) Expand a viable co-operative cross disciplinary forum of EMT-related researchers internationally, particularly with outreach to Asia. This will continue to provide a worldwide network for exchange of expertise, reagents and techniques across disciplines. 4) Publish a timely meeting update on cellular, molecular and genetic aspects of EMT in an appropriate cross-disciplinary international journal.
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Overcoming Barriers to International Clinical Trials for Rare Cancers , December 10, 2010
Description: The goals of this conference were to introduce key institutional players to the topic of international clinical trials in rare cancers and to establish an ongoing dialogue. Participants left the meeting with a set of specific priorities that need to be enacted to promote these trials. The meeting promoted consensus on the way that resources are prioritized to address rare cancers. Participants were asked to convey the content of the meeting to their constituencies and to follow up with pilot concepts.
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VI International Conference on Rare Diseases and Orphan Drugs (ICORD 2010): Global Approach to Accessibility in Rare Diseases, Orphan Drugs and Neglected Diseases , March 18, 2010 - March 20, 2010
Location: Palais Rouge Convention Center, Palermo, Buenos Aires Description: For the first time, the VI International Conference on Rare Diseases and Orphan Drugs (ICORD 2010) was convened in the southern hemisphere in agreement with its aim of globalization of rare diseases research and orphan products development activities.
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Clinical Trials & Research (Found 3 resources)
Resources where you may find research studies and clinical trials. Disclaimer
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ClinicalTrials.gov lists trials that are studying or have studied Adenocarcinoma of the appendix. Click on the link to go to ClinicalTrials.gov to read descriptions of these studies.
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NIH Clinical Trials and You is a website developed by the National Institutes of Health (NIH) to help people learn more about clinical trials, why they matter, and how to participate.
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Patient Registry
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ResearchMatch is a free national research registry designed to bring together patients, healthy volunteers and researchers. Anyone from the United States can register with ResearchMatch, and a parent, legal guardian, or caretaker may register on behalf of a volunteer. Researchers from participating institutions use the ResearchMatch database to search for patients or healthy volunteers who meet the study criteria. Many studies are looking for healthy people of all ages, while some are looking for people with specific illnesses. ResearchMatch was developed by major academic institutions across the country and is funded by the National Center for Advancing Translational Sciences.
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