Parathyroid carcinoma
β Scribed by N. Rawat; N. Khetan; D. W. Williams; J. N. Baxter
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 209 KB
- Volume
- 92
- Category
- Article
- ISSN
- 0007-1323
- DOI
- 10.1002/bjs.5182
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β¦ Synopsis
Abstract
Background
Parathyroid carcinoma is a rare malignancy affecting 0Β·5β5 per cent of all patients with primary hyperparathyroidism. This article reviews the literature on the pathogenesis, pathology, clinical features, diagnosis and management of parathyroid carcinoma.
Methods
A Medline search was performed and all relevant English language articles published between 1970 and 2005 were retrieved. The search words included βparathyroid carcinomaβ, βpathologyβ, βgeneticsβ, βmanagementβ and βradiotherapyβ. Secondary references were obtained from key articles.
Results and conclusion
The exact aetiology of parathyroid carcinoma remains obscure. Recently, the HRPT2 gene has been implicated in its pathogenesis and may prove to be a genetic target in future. Surgical resection is the accepted βgold standardβ. There is now a growing consensus on the use of adjuvant radiotherapy as it has been shown to provide a survival benefit.
π SIMILAR VOLUMES
Parathyroid carcinoma is a rare, reported to be less than 1% of patients with primary hyperparathyroidism. Recently, cell cycle regulators such as the retinoblastoma gene and p53 have been implicated in the pathogenesis of parathyroid carcinoma. Yet definite diagnosis remains difficult not only clin
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## BACKGROUND. Although lung carcinoma is the most common cause of tumorinduced hypercalcemia (TIH), the precise incidence of TIH remains obscure. Furthermore, the role of parathyroid hormone-related protein (PTHrP) has not been clearly elucidated.