Results 31 to 40 of about 1,397,954 (306)
Parathyroid carcinoma is a rare endocrine malignancy. The reported incidence is from 0.5 to 5% of primary hyperparathyroidism cases in various series. The cause is unknown, but clinical correlations with different genetic syndromes exist. Mutations in the HPRT2 gene seem to play a significant role in the pathogenesis of this disease.
Givi, B., Shah, J.P.
openaire +4 more sources
Key Clinical Message Rare cancer originating from parathyroid parenchymal cells. Preoperative diagnosis is often difficult. Presents with normal serum levels of calcium and parathyroid hormone. Treated by en bloc resection.
Alex Mremi+4 more
doaj +1 more source
Papillary thyroid carcinoma is treated with thyroidectomy with or without central lymph node dissection (CLND). The risk of permanent hypoparathyroidism after CLND was calculated. The results that indicated that CLND is an independent risk factor for permanent hypoparathyroidism. CLND is associated with permanent hypoparathyroidism Background Papillary
F. A. Salem+3 more
wiley +1 more source
Thyroid nodules in children and adolescents: Investigation and management
Clinically detectable thyroid nodules are less common in children than adults. However, they are associated with an increased risk of malignancy. Therefore, thorough evaluation of paediatric thyroid nodules is necessary, and an understanding of the features associated with a higher risk of malignancy is important to guide management and referral ...
Jessica L Sandy+5 more
wiley +1 more source
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
Programmed death ligand 1 expression levels, clinicopathologic features, and survival in surgically resected sarcomatoid lung carcinoma [PDF]
Aim: To determine the programmed death ligand-1 (PD-L1) expression rates in sarcomatoid lung carcinomas and to compare clinicopathologic features and survival rates of PD-L1-positive and negative patients. Methods: PD-L1 expression was evaluated in 65 surgically resected sarcomatoid carcinomas.
arxiv +1 more source
Ionized hypercalcemia in 238 cats from a referral hospital population (2009‐2019)
Abstract Background Ionized calcium concentration ([iCa]) is more sensitive for detecting calcium disturbances than serum total calcium concentration but literature on ionized hypercalcemia in cats is limited. Urolithiasis is a possible adverse consequence of hypercalcemia. Hypothesis/Objectives To describe clinical details of diagnoses associated with
Sophie E. Broughton+3 more
wiley +1 more source
Parathyroid Carcinoma – An Uncommon Differential Diagnosis of Pathological Bone Fracture
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
Gastrointestinal symptoms in patients with isolated oligodontia and a Wnt gene mutation
Abstract Objective Since Wnt signaling plays an important role in both tooth agenesis and altered intestine homeostasis, the aim was to compare gastrointestinal symptoms in patients with isolated oligodontia caused by a Wnt pathway gene mutation and controls.
Jamila N. Ross+8 more
wiley +1 more source
Large Retrosternal Parathyroid Carcinoma with Primary Hyperparathyroidism
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