Insulinoma differential diagnosis: Difference between revisions
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Insulinoma must be differentiated from:<ref name="Abboud2008">{{cite journal|last1=Abboud|first1=Bassam|title=Occult sporadic insulinoma: Localization and surgical strategy|journal=World Journal of Gastroenterology|volume=14|issue=5|year=2008|pages=657|issn=1007-9327|doi=10.3748/wjg.14.657}}</ref> | Insulinoma must be differentiated from:<ref name="Abboud2008">{{cite journal|last1=Abboud|first1=Bassam|title=Occult sporadic insulinoma: Localization and surgical strategy|journal=World Journal of Gastroenterology|volume=14|issue=5|year=2008|pages=657|issn=1007-9327|doi=10.3748/wjg.14.657}}</ref> | ||
*Hypoglycemia due to [[sulfonylurea]] or [[insulin]] abuse | *Hypoglycemia due to [[sulfonylurea]] or [[insulin]] abuse | ||
*Autoimmune hypoglycemia | *Autoimmune hypoglycemia | ||
*Factitious hypoglycemia | *Factitious hypoglycemia | ||
*Noninsulinoma pancreatogenic hypoglycemia syndrome (NIPHS) | *Noninsulinoma pancreatogenic hypoglycemia syndrome (NIPHS) | ||
*Familial persistent hyperinsulinemia | *Familial persistent hyperinsulinemia | ||
*[[Nesidioblastosis]] | |||
==References== | ==References== | ||
{{Reflist|1}} | {{Reflist|1}} | ||
Revision as of 13:46, 15 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
Insulinoma must be differentiated from autoimmune hypoglycemia, hypoglycemia due to sulfonylurea or insulin abuse, factitious hypoglycemia, noninsulinoma pancreatogenic hypoglycemia syndrome (NIPHS), familial persistent hyperinsulinemia, and nesidioblastosis.[1]
Differential Diagnosis
Insulinoma must be differentiated from:[1]
- Hypoglycemia due to sulfonylurea or insulin abuse
- Autoimmune hypoglycemia
- Factitious hypoglycemia
- Noninsulinoma pancreatogenic hypoglycemia syndrome (NIPHS)
- Familial persistent hyperinsulinemia
- Nesidioblastosis
References