2008
DOI: 10.1590/s0004-27302008000800021
|View full text |Cite
|
Sign up to set email alerts
|

Pancreatitis as the first manifestation of multiple endocrine neoplasia type 2A

Abstract: Multiple endocrine neoplasia type 2A (MEN2A) is an autosomal dominant inherited condition that predisposes to the triad of medullary thyroid cancer (MTC), pheochromocytoma (Pheo), and primary hyperparathyroidism (PHT). Nearly 100% of MEN2A are associated with germ line mutation of the RET proto-oncogene (RET), and DNA-based RET genotype analysis is now considered essential for earlier diagnosis. The first manifestation of MEN2A is most often due to MTC, and less frequently to Pheo. Rarely, MEN2A is recognized … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

1
1
0

Year Published

2015
2015
2019
2019

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 12 publications
1
1
0
Order By: Relevance
“…Pain surfacing as acute pancreatitis-like syndrome in the presence of chaotic clinical findings similar to those found in our case may be the first manifestation of a pheochromocytoma (PCC) [10, 11], a catecholamine-secreting tumor, originating within the adrenal medullary chromaffin system [12]. However, the levels of catecholamines in 24-h urine collection, specifically metanephrines [13], were normal in our case.…”
Section: Discussionsupporting
confidence: 58%
“…Pain surfacing as acute pancreatitis-like syndrome in the presence of chaotic clinical findings similar to those found in our case may be the first manifestation of a pheochromocytoma (PCC) [10, 11], a catecholamine-secreting tumor, originating within the adrenal medullary chromaffin system [12]. However, the levels of catecholamines in 24-h urine collection, specifically metanephrines [13], were normal in our case.…”
Section: Discussionsupporting
confidence: 58%
“…Other, NOS category is for identified causes of hypercalcemia such as parathyroid tumors (43), multiple endocrine neoplasia (MEN) type 1 or 2a (33,44), other cancers such as multiple myeloma (33,45), or rare causes of hypercalcemia.…”
Section: Toxic-metabolic Factorsmentioning
confidence: 99%