Results 31 to 40 of about 26,263 (201)

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: Update on Pathogenesis and Therapy

open access: yes, 2023
Parathyroid carcinoma (PC) is a very rare endocrine cancer with aggressive behavior, a high metastatic potential, and a poor prognosis. Surgical resection of affected gland(s) and other involved structures is the elective therapy. Pre-operative and intra-
Cinzia Aurilia   +5 more
core   +1 more source

Giant Parathyroid Tumor:Parathyroid Adenoma versus Parathyroid Carcinoma [PDF]

open access: yes, 2022
Parathyroid adenoma is the most common cause of primary hyperparathyroidism (PHPT). We present the preoperative detection of a giant parathyroid adenoma (GPA) using (99mTc)-sestamibi parathyroid scintigraphy in a patient presenting with severely elevated
Carlé, Allan   +5 more
core   +1 more source

Pathology data set for reporting parathyroid carcinoma and atypical parathyroid neoplasm: recommendations from the International Collaboration on Cancer Reporting.

open access: yes, 2021
Standardized pathologic reporting for cancers improves patient care and prognostic determination. However, access in many countries is limited.
Perrier, Nancy D   +11 more
core   +1 more source

Multiple Relapses of Parathyroid Carcinoma with Severe Systemic Complications - Case Report and Literature Review

open access: yes, 2021
Parathyroid carcinoma is an exceptionally uncommon endocrine neoplasm, accounting for less than 1% of parathyroid tumors and also a rare cause of primary hyperparathyroidism.
Bogdan SOCEA   +3 more
core   +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

Updates of Genomics and Proteomics of Parathyroid Carcinoma

open access: yes, 2022
Parathyroid carcinoma is a rare disease that needs an additional diagnostic tool and wide therapeutic options. The genomics and proteomics approach may help to find the tools to improve the prognosis of the disease by early detection and metastatic ...
Sung Hye Kong
core   +1 more source

Two case reports of parathyroid carcinoma and review of the literature

open access: yesJournal of Oncological Sciences, 2017
Parathyroid carcinoma is an infrequent endocrine malignant neoplasm with an aggressive behavior. Two cases of parathyroid carcinoma are described, one with a late diagnosis after previous surgeries for parathyroid hyperplasia, and the other diagnosed ...
Juliana Maria de Almeida Vital   +6 more
doaj   +1 more source

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