A 71-yr-old woman presented with progressive weakness, bone pain, poly
dipsia, and epigastric pain. Laboratory studies established the diagno
sis of primary hyperparathyroidism with excessively elevated levels of
parathyroid hormone (PTH) complicated by renal failure and anemia. Pr
eoperative imaging using (99m)technetium hexakis 2-methoxyisobutylison
itrile (MIBI) demonstrated an area of intense uptake in the mediastinu
m, which on T-2-weighted magnetic resonance imaging revealed the prese
nce of a hyperintense mediastinal mass of 25 mm in diameter adjacent t
o the ascending aorta. Surgical exploration and resection of the mass
were performed, and histological examination of the tumor revealed sol
id masses of epithelial cells growing in a trabecular pattern, hyaline
bands, and low mitotic activity. Immunohistochemical staining of the
tumor specimens using monoclonal mouse antihuman antibodies revealed m
arkedly positive immunoreactivity of tumor cells for p53 protein and a
bsence of nuclear immunoreactivity for the retinoblastoma tumor-suppre
ssor protein, findings consistent with parathyroid carcinoma. Improved
imaging techniques and advances in molecular pathology of parathyroid
disorders may help to improve clinical management of patients with pa
rathyroid neoplasia.