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Parathyroid hyperplasia in primary hyperparathyroidism. A review of 85 cases
Author(s) -
Castleman Benjamin,
Schantz Arthur,
Roth Sanford I.
Publication year - 1976
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/1097-0142(197610)38:4<1668::aid-cncr2820380438>3.0.co;2-x
Subject(s) - medicine , hyperplasia , primary hyperparathyroidism , hypoparathyroidism , hyperparathyroidism , adenoma , pathology , parathyroid gland , parathyroid neoplasm , parathyroid adenoma , parathyroid hormone , calcium
Parathyroid hy perplasia of all four glands was found to be the cause of primary hyperparathyroidism in 85 of 557 cases seen at the Massachusetts General Hospital between 1930 and 1973. There were 66 cases of chief cell hyperplasia and 19 cases of clear cell hyperplasia that were grossly, microscopically, and ultrastructurally distinct. Although the clinical findings overlap, there are several differences in the signs and symptoms between these two forms of hyperplasia. Both types are treated by subtotal removal of all of the parathyroid tissue. Removal of insufficient tissue has left residual hyperparathyroidism in 45% of those with chief cell hyperplasia and 11% of those with clear cell hyperplasia after what was thought to be definitive surgery. Postoperative hypoparathyroidism was found in 15% of the patients with chief cell hyperplasia and in none with clear cell hyperplasia'. These findings further suggest that removal of three and one‐half glands in the more than 86% of patients with one gland involvement (adenoma or carcinoma) as the cause of primary hyperparathyroidism is unwarranted.

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