Results 31 to 40 of about 21,377 (235)

European multicentre study on outcome of surgery for sporadic primary hyperparathyroidism

open access: yesBJS (British Journal of Surgery), EarlyView., 2020
Some 5861 patients undergoing first‐time surgery for sporadic primary hyperparathyroidism were registered in the Eurocrine® database between 2015 and 2018. The use of intraoperative parathyroid hormone measurement decreased the risk of conversion and persistent hypercalcaemia.
A. Bergenfelz   +3 more
wiley   +1 more source

Complications after medullary thyroid carcinoma surgery: multicentre study of the SQRTPA and EUROCRINE® databases

open access: yesBJS (British Journal of Surgery), EarlyView., 2020
This study investigated postoperative complications after surgery for medullary thyroid carcinoma (MTC) in Europe. Hypoparathyroidism, recurrent laryngeal nerve palsy and bleeding requiring reoperation occurred in 170 (26·2 per cent), 62 (13·7 per cent) and 17 (2·6 per cent) patients respectively.
D.‐J. van Beek   +18 more
wiley   +1 more source

Parathyroid Adenoma as a Rare Cause of Persistent Hypercalcemia in a Female with Polycythemia Vera

open access: yesCase Reports in Oncology, 2020
Polycythemia vera is one of the myeloproliferative neoplasms that is distinguished by the uncontrolled production of blood cells and an increased red cell mass due to acquired JAK2 mutation.
Ahmed M. Abdalhadi, Mohamed A. Yassin
doaj   +1 more source

A Rare Presentation of a Bi-Maxillary Brown Tumour due to Secondary Hyperparathyroidism

open access: yesCase Reports in Dentistry, 2023
Brown tumours are localized bone lesions, seen in patients with high parathyroid hormone levels. This can be due to primary hyperparathyroidism, which occurs more often in neoplasms of the parathyroid gland or due to secondary hyperparathyroidism more ...
Cheboh Cho-Fon   +2 more
doaj   +1 more source

Familial Hyperparathyroidism

open access: yesFrontiers in Endocrinology, 2021
Regulation of the serum calcium level in humans is achieved by the endocrine action of parathyroid glands working in concert with vitamin D and a set of critical target cells and tissues including osteoblasts, osteoclasts, the renal tubules, and the ...
Jenny E. Blau   +2 more
doaj   +1 more source

Overview of 2022 WHO Classification of Parathyroid Tumors.

open access: yes, 2022
The 2022 WHO classification reflects increases in the knowledge of the underlying pathogenesis of parathyroid disease. In addition to the classic characteristic features of parathyroid neoplasms, subtleties in histologic features which may indicate an ...
Mete, Ozgur   +4 more
core   +1 more source

Incidentally discovered parathyroid lipoadenoma in thyroid surgery: A case report and review of the literature

open access: yesClinical Case Reports, 2023
Key Clinical Message Parathyroid lipoadenoma is a rare type of parathyroid adenoma, described as a single parathyroid adenoma with more than 50% fat on histologic examination and an unknown etiology, which is one of the rare causes of primary ...
Yihan Wang, Yan Chen, Yantao Fu
doaj   +1 more source

Parathyroid carcinoma

open access: yesJournal of the Belgian Society of Radiology, 2013
Background: A 32-year-old woman with palpable neck mass and clinical presentation of hypercalcemic crisis and primary hyperparathyroidism was referred to radiology and nuclear medicine departments for imaging studies.
A Dilli, SS Gultekin, UY Ayaz
doaj   +1 more source

Ectopic parathyroid adenoma in the upper anterior mediastinum

open access: yesJournal of the Belgian Society of Radiology, 2011
Background: A 66-year-old man, known with nephrocalcinosis in his medical history, was complaining of weight loss, pain at the level of the kidneys and at the right hip. Clinical examination revealed no additional abnormalities.
W Verwimp, P Bracke, H Degryse
doaj   +1 more source

A late diagnosis of MEN 1 Syndrome in a young patient initially pre-senting with nephrolithiasis

open access: yesLiječnički vjesnik, 2023
Multiple Endocrine Neoplasms Type 1 (MEN 1), originally called Wermer Syndrome, is a rare hereditary condition caused by mutations in the MEN1 tumor suppressor gene.
Ana Čala, Tina Dušek
doaj   +1 more source

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