The American Journal of Medicine
Volume 76, Issue 6 , Pages 1021-1026, June 1984

Parathyroid glands in familial benign hypercalcemia (familial hypocalciuric hypercalcemia)

  • William M. Law Jr., M.D.

      Affiliations

    • From the Endocrine Research Unit, Division of Endocrinology and Metabolism, Department of Medicine, and the Department of Pathology, Mayo Clinic, Rochester, Minnesota.
    • Current address: University of Tennessee, Physicians' Office Building, Suite 303, 1928 Alcoa Highway, Knoxville, Tennessee 37920.
  • ,
  • J.Aidan Carney, M.D.

      Affiliations

    • From the Endocrine Research Unit, Division of Endocrinology and Metabolism, Department of Medicine, and the Department of Pathology, Mayo Clinic, Rochester, Minnesota.
  • ,
  • Hunter Heath III, M.D.

      Affiliations

    • Corresponding Author InformationRequests for reprints should be addressed to Dr. Hunter Heath III, Mayo Clinic, 5-164 West Joseph Building, Rochester, Minnesota 55905.
    • From the Endocrine Research Unit, Division of Endocrinology and Metabolism, Department of Medicine, and the Department of Pathology, Mayo Clinic, Rochester, Minnesota.

Rochester, Minnesota USA

Accepted 4 January 1984.

Abstract 

The histologic characteristics of the parathyroid glands in familial benign hypercalcemia (familial hypocalciuric hypercalcemia) are disputed, some finding parathyroid hyperplasia and others finding no abnormalities. To further investigate this issue, the histologic appearance of 82 parathyroid glands from 47 control patients (surgical and autopsy) were compared with those of 28 glands from 23 patients with familial hypocalciuric hypercalcemia who had undergone surgery for suspected primary hyperparathyroidism. Median and mean weights of 23 parathyroid glands from 12 patients with familial hypocalciuric hypercalcemia were 50 mg and 60 mg, respectively, with a range from 5 to 181 mg. Eighty-three percent of individual glands were within extreme normal limits for weight (less than 75 mg). Percent parenchymal area in familial hypocalciuric hypercalcemia was slightly but significantly less than control values (62 ± 2 versus 71 ± 2 percent, respectively; (p = 0.009). Conversely, percent fat was higher in familial hypocalciuric hypercalcemia than control values (30 ± 3 versus 21 ± 2 percent, respectively; p = 0.015). Stromal area was 8 ± 1 percent in each group. Although 15 to 20 percent of parathyroid glands in familial hypocalciuric hypercalcemia exceeded normal size, most were indistinguishable from normal by size, weight, and microscopic appearance. The significantly reduced percent parenchyma in glands from patients with familial hypocalciuric hypercalcemia further suggests that the condition is not uniformly accompanied by typical parathyroid hyperplasia and should not be thought of as merely a variant of the latter.

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 This work was supported in part by grants from the National Institutes of Health (AM-19607) and the Mayo Foundation. Dr. Law was a Research Fellow of the Mayo Foundation and Mayo Graduate School of Medicine.

PII: 0002-9343(84)90852-0

The American Journal of Medicine
Volume 76, Issue 6 , Pages 1021-1026, June 1984