Pheochromocytoma with Endocrinopathy

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Abstract
To the Editor: Manning et al., in the January 10 issue of the Journal, report a case of bilateral familial pheochromocytomas, hyperparathyroidism and thyroid carcinoma. In a recent review of the experience with 11 cases of pheochromocytoma at the Toronto General Hospital from 1948 to 1962, 2 interesting cases of pheochromocytoma with an associated endocrinopathy were noted:G.L., an 18-year-old girl, was first admitted to the hospital in April, 1942, with a history of recurrent pain in the right loin. A diagnosis of bilateral nephrocalcinosis was established by intravenous pyelography, and serum calcium and phosphorus determinations gave evidence of . . .

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