Loss of The Retinoblastoma Tumor-Suppressor Gene in Parathyroid Carcinoma
Parathyroid carcinomas are malignant neoplasms that are an uncommon but often devastating cause of hyperparathyroidism 1 – 3 . These malignant tumors are usually associated with more profound clinical manifestations of hyperparathyroidism than are parathyroid adenomas, the benign, clonal tumors 4 th...
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Published in: | The New England journal of medicine Vol. 330; no. 11; pp. 757 - 761 |
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Main Authors: | , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Boston, MA
Massachusetts Medical Society
17-03-1994
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Subjects: | |
Online Access: | Get full text |
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Summary: | Parathyroid carcinomas are malignant neoplasms that are an uncommon but often devastating cause of hyperparathyroidism
1
–
3
. These malignant tumors are usually associated with more profound clinical manifestations of hyperparathyroidism than are parathyroid adenomas, the benign, clonal tumors
4
that are the most frequent cause of primary hyperparathyroidism. Parathyroid carcinomas may recur locally or metastasize to regional lymph nodes, the lungs, the liver, the pancreas, or bone. Patients with metastatic disease generally die of complications of recurrent hypercalcemia
1
–
3
. The only curative treatment for parathyroid carcinoma is en bloc resection of the primary tumor
1
–
3
. Parathyroid carcinoma and adenoma . . . |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0028-4793 1533-4406 |
DOI: | 10.1056/NEJM199403173301105 |