Parathyroid carcinoma

Author:

Rawat N1,Khetan N1,Williams D W1,Baxter J N1

Affiliation:

1. Department of General Surgery, Morriston Hospital, Swansea, UK

Abstract

Abstract Background Parathyroid carcinoma is a rare malignancy affecting 0·5–5 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 ‘parathyroid carcinoma’, ‘pathology’, ‘genetics’, ‘management’ and ‘radiotherapy’. 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 ‘gold standard’. There is now a growing consensus on the use of adjuvant radiotherapy as it has been shown to provide a survival benefit.

Publisher

Oxford University Press (OUP)

Subject

Surgery

Reference71 articles.

1. Parastruma maligna aberrata;de Quervain;Dtsch Z Chir,1904

2. Malegne dun adenoma parathyroidiene eosinophile; au cours dune de Recklinghausen;Sainton;Annales Anatomie Pathologique,1933

3. Management of cancer of the parathyroid;Rao;Acta Otolaryngol,2002

4. Parathyroid carcinoma;Beus;Otolaryngol Clin North Am,2004

5. Two hundred eighty-six cases of parathyroid carcinoma treated in the US between 1985–1995: a National Cancer Data Base Report. The American College of Surgeons Commission on Cancer and the American Cancer Society;Hundahl;Cancer,1999

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