Multiple endocrine neoplasia type 1 medical therapy: Difference between revisions
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* Excessive release of certain [[hormone]]s mainly [[gastrin]] from pancreatic endocrine cancer in multiple endocrine neoplasia type 1 needs to be treated, and [[medication]]s are often effective in blocking the effects of these [[hormone]]s.<ref>[http://www.niddk.nih.gov/health-information/health-topics/endocrine/multiple-endocrine-neoplasia-type-1/Pages/fact-sheet.aspx] Multiple Endocrine Neoplasia Type 1</ref> | * Excessive release of certain [[hormone]]s mainly [[gastrin]] from pancreatic endocrine cancer in multiple endocrine neoplasia type 1 needs to be treated, and [[medication]]s are often effective in blocking the effects of these [[hormone]]s.<ref>[http://www.niddk.nih.gov/health-information/health-topics/endocrine/multiple-endocrine-neoplasia-type-1/Pages/fact-sheet.aspx] Multiple Endocrine Neoplasia Type 1</ref> | ||
* [[Cabergoline]] is the treatment of choice for [[prolactinoma]]s. | * [[Cabergoline]] is the treatment of choice for [[prolactinoma]]s. | ||
* [[Somatostatin]] analogues such as [[octreotide]] | * [[Somatostatin]] analogues such as [[octreotide]] or [[lanreotide]] are used for the treatment of [[growth hormone]] secreting [[tumor]]s. | ||
* H2- receptor | * [[H2-receptor blocker]]s and [[proton pump inhibitor]]s are used to reduce the gastric output in [[gastrinoma]]s. | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
[[Category:Hereditary cancers]] | [[Category:Hereditary cancers]] |
Revision as of 19:25, 14 September 2015
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [3]
Overview
Pharmacologic medical therapies for multiple endocrine neoplasia type 1 include cabergoline, somatostatin analogues, and H2- receptor blockers.
Management
- Because the type of pancreatic endocrine cancer associated with multiple endocrine neoplasia type 1 can be difficult to recognize, difficult to treat, and slow to progress, there are different views about the value of surgery in managing these tumors.
- One approach is to "watch and wait," using medical, or nonsurgical, treatments. According to this school of thought, pancreatic surgery has serious complications, so it should not be attempted unless it will cure a tumor or cure a hormone excess state.
- Excessive release of certain hormones mainly gastrin from pancreatic endocrine cancer in multiple endocrine neoplasia type 1 needs to be treated, and medications are often effective in blocking the effects of these hormones.[1]
- Cabergoline is the treatment of choice for prolactinomas.
- Somatostatin analogues such as octreotide or lanreotide are used for the treatment of growth hormone secreting tumors.
- H2-receptor blockers and proton pump inhibitors are used to reduce the gastric output in gastrinomas.