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Lymphocytic Adenohypophysitis

Published online by Cambridge University Press:  18 September 2015

Michael W. McDermott ,
Donald E. Griesdale ,
Kenneth Berry  and
G. Edward Wilkins
Michael W. McDermott*
Affiliation:
Divisions of Neurosurgery, Neuropathology, and Endocrinology, University of British Columbia, Vancouver
Donald E. Griesdale
Affiliation:
Divisions of Neurosurgery, Neuropathology, and Endocrinology, University of British Columbia, Vancouver
Kenneth Berry
Affiliation:
Divisions of Neurosurgery, Neuropathology, and Endocrinology, University of British Columbia, Vancouver
G. Edward Wilkins
Affiliation:
Divisions of Neurosurgery, Neuropathology, and Endocrinology, University of British Columbia, Vancouver
*
Department of Surgery, 910 West 10th Avenue, Suite 3100, Vancouver, B.C., Canada V5Z 4E3
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Abstract:

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Lymphocytic adenohypophysitis (LAH) is an uncommon disorder in the spectrum of pituitary disease. Twenty-three cases proven by biopsy or at autopsy have been reported since 1962. We report 2 further cases and review the etiology, immunology and pathology of the disease. The diagnosis should be considered in afemale patient who presents during the post-partum period with the clinical picture of a non-functional or prolactin cell pituitary adenoma and evidence of hypopituitarism.

Type
Original Articles
Information
Canadian Journal of Neurological Sciences , Volume 15 , Issue 1 , February 1988 , pp. 38 - 43
Copyright
Copyright © Canadian Neurological Sciences Federation 1988

References

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