저혈당으로 내원한 뇌하수체 기능저하증을 동반한 빈안장증후군 1예A Case with Empty Sella Syndrome Combined with Multiple Anterior Pituitary Hormone Deficiencies Presenting as Hypoglycemic Coma
- Other Titles
- A Case with Empty Sella Syndrome Combined with Multiple Anterior Pituitary Hormone Deficiencies Presenting as Hypoglycemic Coma
- Authors
- 김수경; 김성수; 김보라; 정정화; 정태식; 함종렬
- Issue Date
- 2014
- Publisher
- 고신대학교(의대) 고신대학교 의과대학 학술지
- Keywords
- ACTH deficiency; Empty sella; Hypoglycemia
- Citation
- 고신대학교 의과대학 학술지, v.29, no.2, pp 151 - 155
- Pages
- 5
- Indexed
- DOMESTIC
- Journal Title
- 고신대학교 의과대학 학술지
- Volume
- 29
- Number
- 2
- Start Page
- 151
- End Page
- 155
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/19484
- DOI
- 029/ksmc029-02-09.pdf
- ISSN
- 2005-9531
2586-7024
- Abstract
- A 55-year-old male was admitted to emergency department with a hypoglycemic shock of unknown origin. He was presented with tonic seizure activity after admission. Initial diagnostic procedure could exclude diabetes mellitus, drug side effects, and exogenous insulin application. Detailed evaluation of the patient's history revealed that the patient had experienced repeated hypoglycemic episodes for 2 years. He was diagnosed with hypothyroidism six years ago. Initial laboratory investigations revealed hypoglycemia, hyponatremia, and low plasma cortisol level (0.18 μg/dL). Sellar magnetic resonance imaging showed empty sella. Replacement therapy with hydrocortisone resulted in the improvement of clinical symptoms. Combined pituitary stimulation test with exception of hypoglycemia induced growth hormone and cortisol stimulation test was performed. The response of thyroid stimulating hormone, prolactin, follicle-stimulating hormone, and luteinizing hormone was normal. We report the case of empty sella syndrome associated with hypoglycemic shock due to with multiple anterior pituitary hormone deficiencies.
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