Tumors of the appendix can be divided into two major groups:
Carcinoid
Tumors
Carcinoid tumors are the most common form, representing
about half of all appendix tumor cases. These tumors are more common in
women, and generally occur in the fourth decade of life. About
two-thirds of carcinoid tumors are found in the tip of the appendix,
where they do not obstruct the opening between the appendix and colon.
In
the majority of cases, carcinoid tumors are small (less than two
centimeters) and have a very low risk of spread to nearby lymph nodes.
Appendectomy (removal of the appendix) is adequate treatment in these
cases. Larger tumors have a slightly higher risk of metastasizing to
surrounding lymph nodes and the liver. Removal of the right colon and
regional lymph nodes is recommended.
More than 85% of patients
with carcinoid tumors of the appendix (even with regional metastases)
have a five-year survival rate.
Most patients have no symptoms.
However, some signs may include:
- Acute appendicitis: most
cases are discovered during surgery for appendicitis
- Carcinoid
syndrome (if spread to liver): flushing, shortness of breath, diarrhea,
heart valve disease on the right side
Non-Carcinoid Tumors
Non-carcinoid
tumors of the appendix originate from the epithelial cells lining the
inside of the appendix. Most of the cells creating these tumors produce a
gelatinous material known as mucin. Due to the anatomic structure of
the appendix and the mucin production of these tumors, patients with
non-carcinoid tumors of the appendix are at risk for spread of tumor
cells and mucin within the abdominal cavity. If left untreated, both
tumor cells and mucin can accumulate over time and lead to
life-threatening bowel obstruction and cachexia (weight loss, muscle
atrophy, significant loss of appetite, fatigue). Prognosis and treatment
for these tumors depend on a number of patient and tumor-related
factors.
Pseudomyxoma peritonei (PMP) is defined by the
presence of acellular (i.e., few, if any, tumor cells) mucin within the
abdominal cavity. The most common presentation of PMP is a
mucin-producing tumor of the appendix whose cells have spread outside
the appendix and into the abdominal cavity. The resulting tumor, which
looks like orange jelly, can get as large as 20-30 pounds.
There
are no PMP-specific symptoms, but some of the more frequent presenting
signs include:
- Increase in abdomen size/girth
- Vague
abdominal discomfort; persistent discomfort in the lower right abdomen
- Pelvic
discomfort
- New hernias
- Bowel obstruction
- Ovarian
masses
Adenocarcinoid tumors, also known as goblet
cell carcinomas, have characteristics similar to both carcinoid and
adenocarcinoma tumors of the appendix. Most patients are diagnosed in
their 50s. The prognosis for these tumors is slightly poorer than that
of carcinoid tumors, with an overall five year survival rate of 78%.
The main presenting symptom is acute or chronic
abdominal pain.