Parathyroid carcinoma is a rare endocrine malignancy derived from the parenchymal cells of the parathyroid glands. It is usually associated with more severe and profound clinical and laboratory manifestations than its more common benign counterparts. Its course is usually indolent but progressive; unlike other malignancies, most patients die because of metabolic complications of parathormone (PTH)-related hypercalcemia rather than tumor invasion and spread. The definitive diagnosis of parathyroid carcinoma may be particularly challenging, since the histology of parathyroid tumors may be equivocal or frankly misleading; for this reason, malignancy is often confirmed on a clinical basis only when local or distant metastases occur. Recent advances in the molecular pathogenesis of the disease will lead to the development of more reliable diagnostic markers.

Parathyroid Cancer

IACOBONE, MAURIZIO;
2012

Abstract

Parathyroid carcinoma is a rare endocrine malignancy derived from the parenchymal cells of the parathyroid glands. It is usually associated with more severe and profound clinical and laboratory manifestations than its more common benign counterparts. Its course is usually indolent but progressive; unlike other malignancies, most patients die because of metabolic complications of parathormone (PTH)-related hypercalcemia rather than tumor invasion and spread. The definitive diagnosis of parathyroid carcinoma may be particularly challenging, since the histology of parathyroid tumors may be equivocal or frankly misleading; for this reason, malignancy is often confirmed on a clinical basis only when local or distant metastases occur. Recent advances in the molecular pathogenesis of the disease will lead to the development of more reliable diagnostic markers.
2012
DISEASES OF THE PARATHYROID GLANDS
9781441955494
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/2508229
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? 1
  • OpenAlex ND
social impact