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Background: Patients with primary hyperparathyroidism and secondary hyperparathyroidism due to celiac disease may both present with high parathyroid hormone and normal calcium levels, but their management differs. This study aimed to assess the frequency of celiac disease evaluation among patients with presumed primary hyperparathyroidism and characterize the impact of preoperative evaluation among patients undergoing parathyroidectomy.
Methods: A single-institution cross-sectional study of adult patients evaluated for initial parathyroidectomy for presumed sporadic primary hyperparathyroidism from January 1, 2010, to July 1, 2024, was completed. All patients were assessed for preoperative celiac disease antibody testing. Among those who underwent parathyroidectomy, preoperative biochemical profiles, prevalence of multigland disease, and persistent disease were compared by celiac disease evaluation status.
Results: Of 2,415 patients (80% female, median age 64 years [55, 70]), 266 (11%) were evaluated for celiac disease, of whom 15 (6%) had positive celiac disease antibodies. Two of 15 patients were confirmed to have celiac disease, in whom primary hyperparathyroidism was recognized after celiac disease treatment. Patients evaluated for celiac disease were more likely female (88% vs 78%, P < .005) and older (median age 65 years [55, 73] vs 63 years [55, 70], P = .04), less frequently presented with high serum calcium (97% vs 99%, P < .005), had higher prevalence of multigland disease (38% vs 30%, P = .01), and similar prevalence of postoperative persistent disease (3% vs 2%, P = .38) compared with those not evaluated. Overall, 2,137 (89%) underwent parathyroidectomy. Patients managed nonoperatively were more frequently evaluated for celiac disease (10% vs 18%, P < .005).
Conclusions: Celiac disease is infrequently diagnosed in patients with presumed primary hyperparathyroidism. Celiac disease diagnosis and treatment may facilitate recognition of primary hyperparathyroidism and should be considered in patients presenting with normocalcemia and high parathyroid hormone.
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http://dx.doi.org/10.1016/j.surg.2025.109488 | DOI Listing |
United European Gastroenterol J
September 2025
Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.
J Travel Med
September 2025
School of Medicine, College of Medicine, Nursing and Health Sciences, University of Galway, Galway, Ireland.
Coeliac disease is a widely prevalent chronic condition, which presents potential challenges during international travel. Our analysis of information provided by national coeliac disease organisations points to the need to make more comprehensive and standardised travel health advice available online to people living with coeliac disease.
View Article and Find Full Text PDFAm J Cardiol
September 2025
Department of Cardiovascular Disease, Mayo Clinic, Phoenix, AZ, USA, 85054; Department of Clinical Genomics, Mayo Clinic, Phoenix, AZ, USA.
Background/objective: Spontaneous coronary artery dissection (SCAD) is increasingly recognized as a cause of acute coronary syndrome and has been associated with extracoronary arteriopathies, such as fibromuscular dysplasia (FMD), aneurysms, and dissections across other vascular beds. However, these associations remain understudied in the literature. This study aims to characterize the prevalence and distribution of extracoronary arteriopathies in a large cohort of SCAD patients.
View Article and Find Full Text PDFDig Dis Sci
September 2025
Avicenna Medical and Dental College, Bedian Road Country Homes, Lahore, Pakistan.
Histopathology
September 2025
Department of Pathology, University of Chicago Medicine, Chicago, Illinois, USA.
Collagenous gastritis (CG) is a rare gastrointestinal disorder characterized by subepithelial collagen deposition and lamina propria inflammation. Despite its first description over four decades ago, the pathogenesis remains unclear, with no standardized pathologic criteria/classification, treatment or established prognosis. A systematic PubMed search identified all English-language case reports, series and observational studies describing CG.
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