- Persistent Craniopharyngeal Canal with Posterior Pituitary Ectopia: A Case Report
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Han D, Kim SH, Kim JY, Lee J, Bae KE
- KMID: 2155283
- J Korean Soc Radiol.
- 2016 Mar;74(3):210-213.
- doi: 10.3348/jksr.2016.74.3.210
Persistent craniopharyngeal canal is a congenital defect between sella turcica and nasopharynx. It is considered to develope from incomplete closure of Rathke's pouch, the precursor of adenohypophysis. Persistent craniopharyngeal canal... -
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- First Male Case of Lymphocytic Hypophysitis in Korea
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Chung HK, Kim DH, Kim SJ, Park BJ, Kim EJ, Myong NH, Choi SJ
- KMID: 2157639
- J Korean Med Sci.
- 2003 Apr;18(2):290-294.
- doi: 10.3346/jkms.2003.18.2.290
Lymphocytic hypophysitis is a rare inflammatory disorder which is caused by autoimmune destruction of the pituitary gland. Almost all reported cases have been in women and the disease is often... -
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- A Case of Partial Hypopituitarism after Recovery from Korean Hemorrhagic Fever
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Kim YJ, Kim MR, Nam MS, Kim YS, Kim SK, Bae SK
- KMID: 2331086
- J Korean Soc Endocrinol.
- 1997 Dec;12(4):584-588.
Heorrhage and infarct-like necrosis of anterior lobe of the pituitary gland is one of the characteristic pathologic findings of the autopsied cases of Korean Hemorrhagic Fever (KHF) patients, but there... -
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- An Epidemiologic Study on Pituitary Diseas
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Lee YS, Shin HH, Cho DH, Lee DB, Kim YJ, Park JH, Lee DH, Chung DJ, Chung MY, Lee TH
- KMID: 2048573
- Chonnam Med J.
- 1998 Dec;34(2):297-308.
Hypopituitarism can be casused by various disease. The present study was performed on Korean patients with hypopituitarism and functional pituitary adenoma, who were examined from 1988 to 1997. One hundred... -
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- The Responses of Pituitary Hormones to the Combined Pituitary Stimulation Test in Hypogonadotropic Hypogonadism
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Yang IM, Woo JT, Kim SW, Kim JW, Kim YS, Choi YK, Park EK, Ahn KJ
- KMID: 2461466
- J Korean Soc Endocrinol.
- 1994 Jun;9(2):93-107.
To classify the causes of hypogonadotropic hypogonadism in Korean patients, and to improve the endocrinologic evaluation for the disease, we retrospectively studied the clinical findings and result of combined pituitary... -
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- A Case of Blindness after Transsphenoid Approach for Pituitary Adenoma Removal: Revision Treatment Experience under Local Anesthesia
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Park HJ, Lim JW, Lim YH, Rho YS
- KMID: 2131862
- J Rhinol.
- 2005 Nov;12(2):120-123.
Pituitary adenoma accounts for 10% to 20% of intracranial tumors. Surgical approach to pituitary adenoma had been performed via craniotomy until the early 20th century, but transsphenoidal approach has been... -
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- A case of two consecutive deliveries in a woman with acromegaly
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Choi H, Lee Y, Chung IH, Koh JH, Kim MJ, Shin YG, Chung CH
- KMID: 2252525
- Korean J Med.
- 2004 Dec;67(6):662-666.
Acromegaly is a rare pituitary disorder and usually results from GH hypersecretion by a somatotroph adenoma. Disturbed pituitary function might lead to infertility or early pregnancy termination. Pregnancy in acromegaly... -
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- Disseminated Cryptococcosis in a Patient with Pituitary Cushing's Disease
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Kang CI, Kim SH, Kim HB, Oh MD, Kim SY, Choe KW
- KMID: 759662
- Korean J Intern Med.
- 2003 Sep;18(3):199-201.
Disseminated cryptococcosis mainly occurs in patients with cell-mediated immunity disorders. A case of disseminated cryptococcosis, in a patient with pituitary Cushing's disease, is reported. Cultures of blood, cerebrospinal fluid (CSF)... -
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- A Case of Idiopathic Granulomatous Hypophysitis
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Chung CH, Song MS, Cho HD, Jeong DS, Kim YJ, Bae HG, Kim SJ
- KMID: 1776528
- Korean J Intern Med.
- 2012 Sep;27(3):346-349.
- doi: 10.3904/kjim.2012.27.3.346
Granulomatous hypophysitis is a rare pituitary condition that commonly presents with enlargement of the pituitary gland. A 31-year-old woman was admitted to the hospital with a severe headache and bitemporal... -
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- Growth Hormone Therapy
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Kim SW
- KMID: 2347644
- J Korean Med Assoc.
- 2002 Feb;45(2):206-215.
- doi: 10.5124/jkma.2002.45.2.206
The safe clinical practice of growth hormone(GH) replacement requires judgement of the overall GH status, however, there is no biological marker for this in adults. In addition, diverse actions of... -
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- Diagnosis and Treatment of Adrenal Insufficiency
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Yoo SJ, Jeong H
- KMID: 2168211
- Hanyang Med Rev.
- 2012 Nov;32(4):203-212.
- doi: 10.7599/hmr.2012.32.4.203
Adrenal insufficiency is caused by either primary adrenal failure or by hypothalamic-pituitary impairment of the corticotropic axis which is predominantly due to long-term glucocorticoid treatment or by pituitary disease. Primary... -
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- GNRH test in Male Hypogonadism
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Hong JY, Lee MS
- KMID: 1912170
- Korean J Urol.
- 1983 Dec;24(6):1083-1088.
GnRH test was performed in male hypogonadism which included hypogonadotrophic hypogonadism, Kallmann's syndrome, oligospermia and azoospermia, total 24 cases. The results were as follows: 1. GnRH test is most useful... -
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- Lymphocytic Hypophysitis with Diabetes Insipidus: Improvement by Methylprednisolone Pulse Therapy
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Jo YS, Lee HJ, Rha SY, Hong WJ, Song CJ, Kim YK, Ro HK
- KMID: 1115230
- Korean J Intern Med.
- 2004 Sep;19(3):189-192.
Lymphocytic hypophysitis is a rare inflammatory disorder in the pituitary gland. The lesion is usually confined to the adenohypophysis. Although the involvement of the posterior pituitary gland or the stalk... -
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- Clinical and Hormonal Analysis of Five New Cases and Eight Previously Reported Cases of Isolated ACTCH Deficiency in Korea
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Oh EY, Kim BJ, Chung YJ, Kim DJ, Hahm JR, Chung JH, Min YK, Lee MS, Lee MK, Kim KW
- KMID: 2199514
- J Korean Soc Endocrinol.
- 1999 Sep;14(3):568-577.
Isolated ACTH deficiency is an uncommon disorder, which is defined by low cortisol production with low or normal plasma ACTH levels and no other pituitary abnormalities. We report five new... -
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- No Significance of the Free Cortisol Index Compared to Total Cortisol in Critically Ill Patients
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Kim KW, Kim SW, Kim HJ, Shin CS, Park SJ, Suh GJ, Kim SY
- KMID: 1497718
- Endocrinol Metab.
- 2011 Jun;26(2):120-125.
- doi: 10.3803/EnM.2011.26.2.120
BACKGROUND: Some patients exhibit an inadequate response of cortisol to stressful conditions; this state is known as critical illness-related corticosteroid insufficiency. These patients have low serum binding protein concentrations, thereby... -
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- The Diagnostic Value of a Low Dose (1ug) Rapid ACTH Stimulation Test to Assess the Adrenocortical Function
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Jung IK, Jeon JS, Park YJ, Shin CS, Park KS, Kim SY, Lee HK, Kim HJ, Kim JH
- KMID: 1999288
- J Korean Soc Endocrinol.
- 1997 Sep;12(3):433-442.
BACKGROUND: Insulin induced hypoglycemia has been used to assess the adrenocortical function, but may be hazardous. The standard rapid ACTH stimulation test has been advocated as a substitute but is... -
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