Carcinoid syndrome natural history, complications and prognosis

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Parminder Dhingra, M.D. [2]

Overview

The presence of liver metastasis is associated with a particularly poor prognosis among patients with carcinoid tumor. Depending on the extent of the tumor at the time of diagnosis, the prognosis may vary. However, the prognosis is generally regarded as poor.

Natural History

Complications

Prognosis

  • Factors that determine the clinical course and outcome of patients with gastrointestinal carcinoid tumors are complex and multifaceted and include the following:[1]
  • The site of origin
  • The size of the primary tumor
  • The anatomical extent of disease
  • Elevated expression of the proliferation antigen Ki-67 and the tumor suppressor protein p53 have been associated with poorer prognosis.
  • Adverse clinical prognostic indicators include:
  • Carcinoid syndrome
  • Carcinoid heart disease
  • High concentrations of the tumor markers urinary 5-HIAA and plasma chromogranin A.
  • In people with the carcinoid syndrome, the tumor has usually spread to the liver, which lowers the survival rate.
  • The outlook is more favorable with new treatment methods, such as sandostatin.
  • Thymic carcinoid tumor are generally thought to carry a poor prognosis due to high rates of recurrence and metastases.[2]

References

  1. "Prognostic Factors".
  2. Thymic carcinoid tumour . Radiopaedia. http://radiopaedia.org/articles/thymic-carcinoid-tumour Accessed on September 24, 2015


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