Important
It is possible that the main title of the report Pseudomyxoma Peritonei
is not the name you expected. Please check the synonyms listing to find
the alternate name(s) and disorder subdivision(s) covered by this report.
Synonyms
- Malignant Appendical Tumor
- Malignant Large Bowel Tumor
- Malignant Large Bowel Cystadenocarcinoma
- Malignant Large Bowel Peritoneal Carcinomatosis
- Mucinous Cystadenoma
- Mucinous Cyst Adenocarcinoma
- Disseminated Peritoneal Adenocarcinoma
- Peritoneal Mucinous Carcinomatosis
- Colloid Carcinoma
- Pseudomyxoma Ovarii
Disorder Subdivisions
General Discussion
Pseudomyxoma Peritonei is a rare malignant growth characterized by the progressive accumulation of mucus-secreting (mucinous) tumor cells within the abdomen and pelvis. The disorder develops after a small growth (polyp) located within the appendix bursts through the wall of the appendix, and spreads mucus-producing tumor cells throughout the surrounding surfaces (e.g., the membrane that lines the abdominal cavity [peritoneum]). As mucinous tumor cells accumulate, the abdominal area becomes swollen and digestive (gastrointestinal) function becomes impaired. Pseudomyxoma Peritonei develops at a variable rate, but may grow at a slower rate (indolent) than other malignancies within the abdomen.
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Resources
American Cancer Society, Inc.
1599 Clifton Road NE
Atlanta, GA 30329
USA
Tel: 4043203333
Tel: 8002272345
Internet: http://www.cancer.org
National Cancer Institute
6116 Execuite Blvd, MSC 8322, Rm 3036A
Bethesda, MD 20892-8322
USA
Tel: 3014353848
Tel: 8004226237
TDD: 8003328615
Internet: http://www.cancer.gov
PMP Pals Network
P.O. Box 6484
Salinas, CA 93912
Tel: (831)424-4545
Fax: (831)424-4545
Email: pmppals@yahoo.com
Internet: http://www.pmppals.org
Friends of Cancer Research
2231 Crystal Drive
Suite 200
Arlington, VA 22202
Tel: (703)302-1503
Fax: (703)302-1568
Email: info@focr.org
Internet: http://www.focr.org
For a Complete Report
This is an abstract of a report from the National Organization for Rare Disorders, Inc. ® (NORD). A copy of
the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains
additional information including symptoms, causes, affected population, related disorders, standard and
investigational treatments (if available), and references from medical literature. For a full-text version of
this topic, see http://www.rarediseases.org/search/rdblist.html
The information provided in this report is not intended for diagnostic purposes. It is provided for
informational purposes only. NORD recommends that affected individuals seek the advice or counsel of
their own personal physicians.
It is possible that the title of this topic is not the name you selected. Please check the Synonyms
listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report.
This disease entry is based upon medical information available through the date at the end of the topic.
Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database
completely current and accurate. Please check with the agencies listed in the Resources section for the
most current information about this disorder.
For additional information and assistance about rare disorders, please contact the National Organization
for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; web site
www.rarediseases.org or email orphan@rarediseases.org
Last Updated:
12/15/2004
Copyright
1991, 1996, 1997, 1999, 2002
National Organization for Rare Disorders, Inc.