Hostname: page-component-848d4c4894-8bljj Total loading time: 0 Render date: 2024-07-01T19:35:17.106Z Has data issue: false hasContentIssue false
  • English
  • Français

Langerhan's cell histiocytosis in the sphenoid sinus: a case of diabetes insipidus

Published online by Cambridge University Press:  29 June 2007

S. S. M. Hussain ,
R. D. Simpson ,
D. McCormick  and
C. I. Johnstone
S. S. M. Hussain*
Affiliation:
Registrar in Otolaryngology, Queen Alexandra Hospital, Ports-mouth
R. D. Simpson
Affiliation:
Senior Registrar in Histopathology, Queen Alexandra Hospital, Ports-mouth
D. McCormick
Affiliation:
Consultant Physician, Queen Alexandra Hospital, Ports-mouth
C. I. Johnstone
Affiliation:
Consultant Otolaryngologist, St Richard's Hospital, Chichester
*
Mr S. S. M. Hussain, Department of Otolaryngology, Queen Alexandra Hospital, Portsmouth PO6 3LY
Get access Rights & Permissions [Opens in a new window]

Abstract

We present a case of diabetes insipidus in a young man caused by Langerhan's cell histiocytosis of the sphenoid sinus with involvement of the pituitary gland. Diagnosis and management of this rare condition is discussed, along with a brief view of the literature.

Type
Clinical Records
Information
The Journal of Laryngology & Otology , Volume 103 , Issue 9 , September 1989 , pp. 877 - 879
Copyright
Copyright © JLO (1984) Limited 1989

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Broadbent, V. and Pritchard, J. (1985) Histiocytosis X current controversies. Archives of Disease in Childhood, 60: 605–607.CrossRefGoogle ScholarPubMed
Broadbent, V., Pritchard, J., Davies, E. G., Levensky, R. J., Heaf, D., Atherton, D. J., Pincott, J. R. and Tucker, S. (1984) Spontaneous remission of multi system histiocytosis X. Lancet, 253–254.CrossRefGoogle ScholarPubMed
Green, I., Behar, A. J., Shannon, E. and Gorsky, M. (1988) Multifocal extraosseous eosinophilic granuloma of the head and neck. Archives of Otolaryngology, 114: 561–563.CrossRefGoogle ScholarPubMed
Greenberger, J. S., Crocker, A. C., Vawter, G., Jaffe, N. and Cassidy, J. R. (1981) Results of treatment of 127 patients with systemic histiocytosis. Medicine, 60: 311–338.CrossRefGoogle ScholarPubMed
Lichtenstein, L. (1953) Histiocytosis X. Archives of Pathology, 56: 84–102.Google ScholarPubMed
Osband, M. E., Jeffrey, M. D., Lipton, M., Lavin, P., Levey, R., Vawter, G., Greenberger, J. S. and McCaffery, R. P. (1981) Histiocytosis X demonstration of abnormal imminity, T cell histamine H2 receptor deficiency and successful treatment with thymic extract. New England Journal of Medicine, 304: 146–153.CrossRefGoogle Scholar
Serrano Galnares, J., Gella Lobo, E., Wilhelmi Ayza, M., Gonzalez Ripoli, M. and Moratinos Palomero, P. (1981) Un caso de enermedad de Letterer-Siwe. Anales Espanoles de Pediatria, 14: 444–448.Google Scholar
Smith, D. G., Nesbit, M. E., D'Angio, G. J. and Levitt, S. H. (1973) Histiocytosis X: role of radiation therapy in management with special reference to dose levels employed. Radiology, 106: 419–422.CrossRefGoogle ScholarPubMed
Thiebot, J., Clavier, E., Challine, B. and Henry, J. (1987) Localisation tumorale sphenoidale isolee chez un enfant revelatrice d'une histiocytose X. Journal de Radiologie, 68: 309–311.Google ScholarPubMed