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Highly aggressive pathology of non-functional parathyroid carcinoma

Overview of attention for article published in Orphanet Journal of Rare Diseases, August 2013
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Title
Highly aggressive pathology of non-functional parathyroid carcinoma
Published in
Orphanet Journal of Rare Diseases, August 2013
DOI 10.1186/1750-1172-8-115
Pubmed ID
Authors

Doina Piciu, Alexandru Irimie, George Kontogeorgos, Andra Piciu, Rares Buiga

Abstract

Parathyroid carcinoma is a rare malignant endocrine tumor accounting for only 0.5% to 5% of all primary hyperparathyroidism. Among these malignancies, only 10-25% are nonfunctioning. After the review of the literature we could only ascertain a number of 25 cases reported worldwide, since 1929, our case being the 26th, but the first with a very aggressive pathology, treated with chemotherapy scheme usually used for neuroendocrine tumors. Considering these facts, every single case presented is a step forward in defying the clinical presentation, for the awareness of the clinicians, and also in establishing standard adjuvant therapies.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 12 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Romania 1 8%
Unknown 11 92%

Demographic breakdown

Readers by professional status Count As %
Researcher 4 33%
Student > Ph. D. Student 2 17%
Lecturer 1 8%
Student > Master 1 8%
Student > Postgraduate 1 8%
Other 0 0%
Unknown 3 25%
Readers by discipline Count As %
Medicine and Dentistry 5 42%
Psychology 1 8%
Unknown 6 50%