2021, Number 1
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Rev Fac Med UNAM 2021; 64 (1)
Multiple Endocrine Neoplasia IIA: Bilateral Pheochromocytoma About a Case and Literature Review
Maldonado GEL, Nacud BYA, Gómez VCM, Morfín VC, Guerra MJC
Language: Spanish
References: 11
Page: 26-31
PDF size: 237.47 Kb.
ABSTRACT
We present the case of a 54-year-old female patient with a
family history of multiple endocrine neoplasia type II, with
a genetic study for MEN 2 IIA EXON 11, CG6B c634, onset
with hypertensive heart disease and diastolic dysfunction,
tomographic finding of bilateral adrenal tumor by imaging. A
conventional transabdominal adrenalectomy was performed,
finding a right tumor with a capsule corresponding to pheochromocytoma
with a weight of 1,100 g of 14.5 cm of greater
diameter with invasion of the capsule without breaking it, and
a left adrenal tumor corresponding to pheochromocytoma
with a weight of 950 g of 15 cm of greater diameter.
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