Glucagonoma natural history, complications and prognosis: Difference between revisions
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==Natural History== | ==Natural History== | ||
*If left untreated, patients with carcinoid syndrome may progress to develop ecrolytic migratory erythema, cheilosis, stomatitis, diarrhea, polyuria, and polydipsia. | |||
*They have a very slow growth rate compared to most malignant tumors. | |||
==Prognosis== | ==Prognosis== |
Revision as of 17:40, 13 October 2015
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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
Natural History
- If left untreated, patients with carcinoid syndrome may progress to develop ecrolytic migratory erythema, cheilosis, stomatitis, diarrhea, polyuria, and polydipsia.
- They have a very slow growth rate compared to most malignant tumors.
Prognosis
For approximately 60% of these tumors are cancerous, the prognosis of glucagonoma depends on the following:
- Whether or not the tumor can be removed by surgery
- The stage of the tumor: the size of the tumor, whether the cancer has spread outside the pancreas
- The patient’s general
- Whether the tumor has just been diagnosed or has recurred
- The presence of metastasis is associated with a particularly poor prognosis among patients with glucagonoma. The 10 year event free survival rate is less than 51.6% with metastasis and 64.3% without metastasis.
References