Multiple endocrine neoplasia phenocopy revealed as a co‐occurring neuroendocrine tumor and familial hypocalciuric hypercalcemia type 3
S Hovden, ML Jespersen, PH Nissen… - Clinical Case …, 2016 - pmc.ncbi.nlm.nih.gov
S Hovden, ML Jespersen, PH Nissen, PL Poulsen, L Rolighed, SA Ladefoged, L Rejnmark
Clinical Case Reports, 2016•pmc.ncbi.nlm.nih.govKey Clinical Message Familial hypocalciuric hypercalcemia type 3 should be considered as
differential diagnosis in patients with suspected primary hyperparathyroidism and/or
suspected multiple neoplasia syndrome, as correct diagnosis will spare the patients for
going through multiple futile parathyroidectomies and for the worry of being diagnosed with
a cancer susceptibility syndrome.
differential diagnosis in patients with suspected primary hyperparathyroidism and/or
suspected multiple neoplasia syndrome, as correct diagnosis will spare the patients for
going through multiple futile parathyroidectomies and for the worry of being diagnosed with
a cancer susceptibility syndrome.
Key Clinical Message Familial hypocalciuric hypercalcemia type 3 should be considered as differential diagnosis in patients with suspected primary hyperparathyroidism and/or suspected multiple neoplasia syndrome, as correct diagnosis will spare the patients for going through multiple futile parathyroidectomies and for the worry of being diagnosed with a cancer susceptibility syndrome.
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