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Case Reports in Endocrinology
Volume 2012, Article ID 931371, 4 pages
http://dx.doi.org/10.1155/2012/931371
Case Report

Posterior Fossa Arachnoid Cyst Masking a Delayed Diagnosis of Hyperparathyroidism in a Child

Department of Neurosurgery, Birmingham Children’s Hospital, Steelhouse Lane, Birmingham B4 6NH, UK

Received 8 September 2012; Accepted 31 October 2012

Academic Editors: C. Capella, E. Hershkovitz, and H. Ikeda

Copyright © 2012 B. Dhamija et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. H. Heath, S. F. Hodgson, and M. A. Kennedy, “Primary hyperparathyroidism. Incidence, morbidity, and potential economic impact in a community,” The New England Journal of Medicine, vol. 302, no. 4, pp. 189–193, 1980. View at Google Scholar · View at Scopus
  2. G. R. Mundy, D. H. Cove, and R. Fisken, “Primary hyperparathyroidism: changes in the pattern of clinical presentation,” The Lancet, vol. 1, no. 8182, pp. 1317–1320, 1980. View at Google Scholar · View at Scopus
  3. D. Damiani, C. H. Aguiar, V. S. Bueno et al., “Primary hyperparathyroidism in children: patient report and review of the literature,” Journal of Pediatric Endocrinology and Metabolism, vol. 11, no. 1, pp. 83–86, 1998. View at Google Scholar · View at Scopus
  4. J. Kollars, A. E. Zarroug, J. Van Heerden et al., “Primary hyperparathyroidism in pediatric patients,” Pediatrics, vol. 115, no. 4, pp. 974–980, 2005. View at Publisher · View at Google Scholar · View at Scopus
  5. M. L. Lawson, S. F. Miller, G. Ellis, R. M. Filler, and S. W. Kooh, “Primary hyperparathyroidism in a paediatric hospital,” QJM, vol. 89, no. 12, pp. 921–932, 1996. View at Google Scholar · View at Scopus
  6. K. R. Makhdoomi, J. Chalmers, I. W. Campbell, and G. G. P. Browning, “Delayed diagnosis of juvenile primary hyperparathyroidism,” Journal of the Royal College of Surgeons of Edinburgh, vol. 41, no. 5, pp. 351–353, 1996. View at Google Scholar · View at Scopus
  7. M. S. Kappy, R. M. Blizzard, and C. J. Migeon, The Diagnosis and Treatment of Endocrine Disorders in Childhood and Adolescence. 1056–1061, Charles C Thomas, Springfield, Ill, USA, 1994.
  8. S. C. Hsu and M. A. Levine, “Primary hyperparathyroidism in children and adolescents: the Johns Hopkins Children's Center experience 1984–2001,” Journal of Bone and Mineral Research, vol. 17, supplement 2, pp. N44–N50, 2002. View at Google Scholar · View at Scopus
  9. K. C. Loh, Q. Y. Duh, D. Shoback, L. Gee, A. Siperstein, and O. H. Clark, “Clinical profile of primary hyperparathyroidism in adolescents and young adults,” Clinical Endocrinology, vol. 48, no. 4, pp. 435–443, 1998. View at Publisher · View at Google Scholar · View at Scopus
  10. A. J. Ross, A. Cooper, M. F. Attie, and H. C. Bishop, “Primary hyperparathyroidism in infancy,” Journal of Pediatric Surgery, vol. 21, no. 6, pp. 493–499, 1986. View at Google Scholar · View at Scopus
  11. S. J. Marx, M. F. Attie, and M. A. Levine, “The hypocalciuric or benign variant of familial hypercalcemia: clinical and biochemical features in fifteen kindreds,” Medicine, vol. 60, no. 6, pp. 397–412, 1981. View at Google Scholar · View at Scopus
  12. T. Stefenelli, C. Abela, H. Frank et al., “Cardiac abnormalities in patients with primary hyperparathyroidism: implications for follow-up,” Journal of Clinical Endocrinology and Metabolism, vol. 82, no. 1, pp. 106–112, 1997. View at Publisher · View at Google Scholar · View at Scopus
  13. C. R. Harman, J. A. Van Heerden, D. R. Farley, C. S. Grant, G. B. Thompson, and K. Curlee, “Sporadic primary hyperparathyroidism in young patients: a separate disease entity?” Archives of Surgery, vol. 134, no. 6, pp. 651–656, 1999. View at Publisher · View at Google Scholar · View at Scopus
  14. E. M. Brown, “Editorial: mutant extracellular calcium-sensing receptors and severity of disease,” Journal of Clinical Endocrinology and Metabolism, vol. 90, no. 2, pp. 1246–1248, 2005. View at Publisher · View at Google Scholar · View at Scopus
  15. M. R. Pollak, E. M. Brown, Y. H. W. Chou et al., “Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism,” Cell, vol. 75, no. 7, pp. 1297–1303, 1993. View at Publisher · View at Google Scholar · View at Scopus
  16. F. Raue, C. Haag, E. Schulze, and K. Frank-Raue, “The role of the extracellullar calcium-sensing receptor in health and disease,” Experimental and Clinical Endocrinology and Diabetes, vol. 114, no. 8, pp. 397–405, 2006. View at Publisher · View at Google Scholar · View at Scopus
  17. E. M. Brown, “The pathophysiology of primary hyperparathyroidism,” Journal of Bone and Mineral Research, vol. 17, supplement 2, pp. N24–N29, 2002. View at Google Scholar · View at Scopus