Results 11 to 20 of about 43,074 (235)

Clinical and molecular characterization of parathyroid carcinoma in multiple endocrine neoplasia type 1

open access: yesEndocrine Connections, 2023
Nineteen cases of parathyroid carcinoma in patients with multiple endocrine neoplasia type 1 have been reported in the literature, of which 11 carry an inactivating germline mutation in the MEN1 gene.
Sara Lomelino Pinheiro   +5 more
doaj   +1 more source

Synchronous intrathyroidal parathyroid carcinoma and thyroid carcinoma: case report and review of the literature

open access: yesBMC Endocrine Disorders, 2021
Background Parathyroid carcinoma is a rare endocrine malignancy, rarer when synchronous with a non medullary well differentiated thyroid carcinoma. Parathyroid carcinoma accounts of 0.005% of all malignant tumors and it is responsible for less than 1% of
Nadia De Falco   +11 more
doaj   +1 more source

Challenges in the Diagnosis of Parathyroid Cancer: Unraveling the Diagnostic Maze

open access: yesReports, 2023
Parathyroid carcinoma (PC) is a rare and aggressive cancer affecting the parathyroid glands, presenting diagnostic and therapeutic challenges due to its rarity and overlapping features with benign parathyroid disease.
Mihaela Stanciu   +5 more
doaj   +1 more source

Left parathyroid carcinoma with secondary hyperparathyroidism: a case report

open access: yesBMC Endocrine Disorders, 2023
Background Parathyroid carcinoma is a rare disease with a frequency of 0.005% of all malignancies [1, 2]. Various aspects of its pathogenesis, diagnosis, and treatment remain poorly understood.
Ko Yokoyama   +2 more
doaj   +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 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   +3 more
  +9 more sources

Parathyroid Carcinoma

open access: yesOtolaryngologic Clinics of North America, 2010
Parathyroid carcinoma is a rare tumor that is prone to recurrence and poor local-regional control. Despite advances in technologies that have shown promise for accurate diagnosis, the mainstay of initial diagnosis remains pathologic analysis and clinical assessment.
W Cross, Dudney   +2 more
openaire   +4 more sources

Parathyroid Carcinoma – An Uncommon Differential Diagnosis of Pathological Bone Fracture

open access: yesJournal of Head & Neck Physicians and Surgeons, 2023
We present a case of an unusual presentation of parathyroid carcinoma. A women in her 40s presented with pathological fracture without any other symptom. All her investigations pointed towards an abnormally functioning parathyroid gland.
Kantamani Bala Teja   +2 more
doaj   +1 more source

Large Retrosternal Parathyroid Carcinoma with Primary Hyperparathyroidism

open access: yesAsian Journal of Surgery, 2007
Parathyroid carcinoma is an uncommon cause of parathyroid hormone (PTH)-dependent hypercalcaemia, accounting for less than 1% of all cases of hyperparathyroidism.
Geok Chin Tan   +4 more
doaj   +1 more source

Parathyroid Carcinoma Manifesting as Recurrent Nephrolithiasis

open access: yesPhilippine Journal of Otolaryngology Head and Neck Surgery, 2015
Objective: To present a rare case of primary parathyroid carcinoma and discuss its clinical findings and management. Methods: Study Design:             Case Report Setting:                        Tertiary Government Hospital Patient:          
Ma. Melizza S. Villalon, Celso V. Ureta
doaj   +1 more source

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