The case of Vanishing metatarsal: a rare manifestation of primary hyperparathyroidism has been published in BMJ Case Reports.
A 31-year-old woman presented with a history of bone pains, difficulty in walking and painless swelling of the left foot for the last 1 year (figure 1). X-ray of the left foot showed multiple lytic lesions in metatarsal bones and the absence of proximal half of shaft of second metatarsal. Biochemistry results revealed corrected serum calcium 11.2 mg/dL, phosphate 2.0 mg/dL, alkaline phosphatase 1049 IU/mL, intact parathyroid hormone (iPTH) 2543 pg/mL, 25-hydroxyvitamin D 16.2 ng/mL, and serum creatinine 0.6 mg/dL. She had no history of pancreatitis or evidence of renal/gall stone disease. The skeletal survey showed multiple osteitis fibrosa cystica (OFC) lesions, pathological fracture of shaft of the left femur and salt and pepper appearance of the skull (figure 2a, b, c). Sestamibi scan revealed right inferior parathyroid adenoma measuring 3.0×2.9×2.2 cm. Based on the above findings, a diagnosis of primary hyperparathyroidism (PHPT) was made and she underwent parathyroid adenectomy. Tumour weighed 4 g and histopathology was consistent with clear cell parathyroid adenoma.
The classic bone disease of PHPT, OFC is seen in <2% of patients. In severe and long-standing disease, elevated PTH causes increased osteoclast activity resulting in localised alterations in the trabecular pattern, demineralisation and replacement of marrow by loose connective tissue, leading to radiographic disappearance of bones, as was seen in our patient. They are most commonly seen in flat bones, however, metacarpals and metatarsals are very rarely involved. Differentials of vanishing bone disease besides PHPT include osteomyelitis, Charcot’s neuroarthropathy, rheumatoid arthritis, osseous metastasis and Gorham’s disease.
Contributors VSS: managed the case and prepared the manuscript. AB: conceived the idea and edited the manuscript.
Competing interests None declared.
Patient consent Obtained.
Provenance and peer review Not commissioned; externally peer reviewed.