Results 91 to 100 of about 370,756 (269)
Rare Somatic MEN1 Gene Pathogenic Variant in a Patient Affected by Atypical Parathyroid Adenoma
Objective. Atypical parathyroid adenoma is a rare neoplasm, showing atypical histological features intermediate between classic benign adenoma and the rarest parathyroid carcinoma, whose the clinical behaviour and outcome is not yet understood or ...
Luigia Cinque+12 more
doaj +1 more source
Background Brown tumors are benign osteoclastic bone lesions encountered in patients with hyperparathyroidism. These tumors may demonstrate aggressive, destructive features in the skeleton and imitate metastatic bone lesions, particularly in patients ...
Ula Al-Rasheed+2 more
doaj +1 more source
Background Tumor-induced osteomalacia (TIO) is a rare, acquired disease of renal phosphate wasting and disturbed vitamin D homeostasis as a result of the action of a phosphaturic protein – FGF-23, produced by a neoplasm.
Agnieszka Brociek-Piłczyńska+6 more
semanticscholar +1 more source
The fusion peptide LR27‐modified thermosensitive nanodelivery system exhibits both hair cell targeting and inner ear penetrating properties. This system sustainably and effectively delivers PTH1‐34 to the inner ear of a hearing loss mouse model via the synergistic effects of multiple peptides, achieving satisfactory hearing protection through ...
Jiawen Li+12 more
wiley +1 more source
In patients with femoral head necrosis, strong positive reaction of LC3‐II could be identified in the cytoplasm of osteoclasts, in significant contrast to the background. A trabecula was surrounded by several LC3‐II‐positive osteoclasts, which were in close contact with the trabecula.
Bo Liu+7 more
wiley +1 more source
A patient with femoral osteitis fibrosa cystica mimicking bone neoplasm: a case report
Background Osteitis fibrosa cystica is a rare, benign and osteolytic lesion attributed to hyperparathyroidism. The high level of parathyroid hormone cause rapid bone loss.
Xiao-long Xu+5 more
semanticscholar +1 more source
NIBAN2 interacts with the HNRNPU‐cored spliceosome complex and alters its components to regulate the alternative splicing of RUNX2, which ultimately cause an increase in functional RUNX2 (nuclear localization sequence complete) but a decrease in dysfunctional Runx2 (exon 6‐exclusive) isoforms to reinforce osteoblast differentiation.
Sheng Zhang+9 more
wiley +1 more source
Intrathyroidal Parathyroid Carcinoma: An Atypical Thyroid Lesion
Parathyroid carcinoma is a rare endocrine malignancy that is typically difficult to diagnose at presentation. Here, we report a 63 year-old man who had symptomatic hypercalcemia.
Noran Alharbi+6 more
doaj +1 more source
Hypercalcemia in the Presence of an Ectopic Mediastinal Mass
A 72-year-old gentleman who presented to the outpatient clinic for a preventive health appointment with symptoms of depression and fatigue was found to have persistent hypercalcemia on routine laboratory monitoring.
Robert K. Strother, Matthew Meunier MD
doaj +1 more source
Parathyroid adenoma is associated with both primary and secondary hyperparathyroidism (SHPT). Identification of the adenoma requires a combination of clinical evidence, imaging information and cytological findings due to the challenging distinction ...
M. Yadav+5 more
semanticscholar +1 more source