101. A Case of Lymphocytic Infundibuloneurohypophysitis Along with Central Diabetes Insipidus, and this Improved with Conservative Care
- Author
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Ho Young Son, Byung Hee Hwang, Sung Koo Kang, Ji Myoung Lee, Sung Rae Kim, Kwang Woo Lee, Jee Young Kim, Seong Su Lee, Soon Jib Yoo, Sang Mi Park, and Hyun Sook Choi
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Pituitary stalk ,Autoimmune disease ,medicine.medical_specialty ,Pathology ,Pituitary gland ,medicine.diagnostic_test ,Hypophysitis ,business.industry ,Context (language use) ,Magnetic resonance imaging ,medicine.disease ,Lesion ,Endocrinology ,medicine.anatomical_structure ,Internal medicine ,Diabetes insipidus ,medicine ,medicine.symptom ,business - Abstract
Idiopathic central diabetes insipidus is most likely to occur in young patients who have a clinical history of autoimmune disease. The presentation of clinical findings such as central diabetes insipidus and pituitary stalk thickening on sellar magnetic resonance imaging (MRI) in a young women would strongly suggest lymphocytic hypophysitis, which is a rare inflammatory process involving the pituitary stalk and the pituitary gland, yet this disease can sometimes regress. We describe here a young woman with lymphocytic hypophysitis. She suffered from an abrupt onset of central diabetes insipidus. Sellar MRI showed thickening of pituitary stalk and loss of high signal of normal neurohypophysis on T1-weighted image. Combind pituitary stimuat ion test showed a blunted response of GH. To avoid the potential detrimental complications of invasive diagnostic procedures for testing the pituitary function in a fertile unmarried young woman, we chose close clinical and radiologic follow-up in the proper clinical context. The requirement for DDAVP was slightly decreased over time and the MR imaging obtained serially for 6 months revealed spontaneous partial regression of the pituitary lesion. (J Korean Endocr Soc 23:142~147, 2008)
- Published
- 2008
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