Exp Clin Endocrinol Diabetes 2008; 116(8): 487-490
DOI: 10.1055/s-2007-992155
Article

© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

A Case of Parathyroid Carcinoma with Severe Hungry Bone Syndrome and Review of Literature

M. S. Rathi 1 , R. Ajjan 1 , S. M. Orme 1
  • 1Department of Endocrinology, Leeds General Infirmary, Leeds, LS1 3EX, United Kingdom
Further Information

Publication History

received 12.07.2007 first decision 02.10.2007

accepted 11.10.2007

Publication Date:
20 December 2007 (online)

Preview

Abstract

We present a 45 year old female who was initially seen by Rheumatologist with long standing knee pain affecting her mobility. She was found to be severely hypercalcaemic and exhibited features suggestive of parathyroid carcinoma (palpable neck mass, extremely high parathyroid hormone, high alkaline phosphatase, concomitant presence of renal disease and skeletal involvement). Hence she was referred for parathyroidectomy.

Postoperatively she developed profound hypocalcaemia with markedly raised serum alkaline phosphatase, requiring intensive intravenous calcium and oral vitamin D supplements, consistent with the development of hungry bone syndrome (HBS).

HBS is a complication of parathyroid surgery where the correction of primary hyperparathyroidism is associated with rapid bone remineralisation, causing severe and prolonged hypocalcaemia.

HBS is relatively rare but has to be considered in the differential diagnosis of postoperative hypocalcaemia particularly in severe cases.

In the current report, we discuss pathogenesis, clinical course and management of HBS.

References

Correspondence

Dr. M.S. Rathi

Department of Endocrinology

Leeds General Infirmary

Great George Street

LEEDS

LS1 3EX

United Kingdom

Phone: +44/113/392 66 93

Fax: +44/113/392 31 50

Email: manjusharathi@hotmail.com