Scinovex
article Open Access

Vanishing bone disease-like presentation in a middle-aged male due to primary hyperparathyroidism: A rare presentation

International Journal of Case Reports in Orthopaedics · 2025 · Vol. 7(1) · pp. 97–99

Abstract

Vanishing bone disease (VBD), also known as Gorham-Stout disease, is typically idiopathic and characterized by progressive osteolysis. However, secondary causes mimicking VBD-like bone loss must be considered, especially in adults. We present a rare case of a 46-year-old male with progressive femoral osteolysis and renal calculi, ultimately diagnosed with primary hyperparathyroidism (PHPT) due to a parathyroid adenoma. Following parathyroidectomy surgery value of parathyroid hormone (PTH) reduced significantly and patient improved clinically. This case highlights the importance of metabolic and endocrine evaluation in osteolytic conditions and demonstrates a reversible form of “vanishing” bone loss.

Dermatological and Skeletal DisordersSystemic Sclerosis and Related DiseasesRNA regulation and diseasePresentation (obstetrics)Primary hyperparathyroidismMedicineCase presentationHyperparathyroidismDiseaseRare diseasePediatricsSurgeryInternal medicine
Citations
0
FWCI
0.00
field-weighted impact
References
4
Percentile
18%
vs. same field & year
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.

Vanishing bone disease-like presentation in a middle-aged male due to primary hyperparathyroidism: A rare presentation · Scinovex