- A Case of Congenital Hypopituitarism with Anterior Pituitary Aplasia and Ectopic Posterior Pituitary Gland
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Jung YS, Lim IS
- KMID: 1515007
- J Korean Soc Pediatr Endocrinol.
- 2003 Dec;8(2):174-178.
Congenital hypopituitarism is a rare disorder with absence or reduction of hormones produced by the pituitary gland. The clinical manifestations are hypoglycemia, prolonged jaundice, hyponatremia, micropenis, underdeveloped clitoris, lethargy, convulsion,... -
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- Hypothalamic Hypopituitarism Caused by Pituitary Stalk Dysgenesis
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Lee SJ, Yoon HJ, Cho AR, Um YJ, Park KY, Lim DM, Kim BJ
- KMID: 2267795
- Korean J Med.
- 2013 Oct;85(4):420-424.
Functional defects of the pituitary gland are a rare cause of pubertal delay. The pituitary stalk is an important structure that connects the hypothalamus and pituitary gland. A defect in... -
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- Clinical Features of Pityitary Hyperplasia
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Kim KR, Lim SK, Won YJ, Kwon SH, Cha BS, Song YD, Lee HC, Huh KB, Choung BY, Nam SY, Kim SH, Kim TS, Um JH
- KMID: 2331057
- J Korean Soc Endocrinol.
- 1997 Jun;12(2):155-164.
BACKGROUNDS: Pituitary hyperplasia can mimic pituitary adenoma. In MRI, enlarged pituitary gland is enhanced homogenously with upward convexity of the superior margin of the gland .The best definition of hyperplasia... -
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- Abnormalities of Hypothalamic-Pituitary MR Imaging and Pituitary Function in Patients with Growth Hormone Deficiency
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Kim HG, Yoo HW
- KMID: 2207870
- J Korean Pediatr Soc.
- 1998 Jun;41(6):791-798.
PURPOSE: In this study, efforts have been made to evaluate the sella MRI in 14 patients with growth hormone deficiency to define more clearly the structural abnormalities of the hypothalamo-... -
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- Changes in Endocrine Function with Treatment of Intracranial Germ Cell Tumor
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Lim JS, Hwang JS, Kim SY, Sim KS, Shin CH, Yang SW, Hwang YS, Ahn HS
- KMID: 2335357
- J Korean Pediatr Soc.
- 1998 Aug;41(8):1120-1127.
PURPOSE: We observed changes in the pituitary function before and after treatment and followed up on the weight and height after treatment in children with intracranial germ cell tumor. METHODS:... -
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- Primary empty sella syndrome
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Kim KR, Lim SK, Song YD, Lee HC, Huh KB, Kim ES, Kim IJ, Moon YJ, Na SK, Nam SY, Lee EJ
- KMID: 1999284
- J Korean Soc Endocrinol.
- 1997 Sep;12(3):386-392.
BACKGROUND: Primary empty sella syndrome (PES) is thought to arise from an incompetent diaphragma allowing progressive herniation of arachnoid membrane with secondary compression and atrophy of the pituitary gland. As... -
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- A Case of Turner's Syndrome with Transient Hypopituitarism
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Nam JS, Cho MH, Roh JM, Kim HJ, Yoon JE, Jung HY, Park JS, Kang ES, Ahn CW, Cha BS, Lee EJ, Lim SK, Kim KR, Lee HC
- KMID: 2063536
- J Korean Endocr Soc.
- 2007 Aug;22(4):266-271.
- doi: 10.3803/jkes.2007.22.4.266
Turner's syndrome is characterized by short stature and gonadal dysgenesis, and it is often associated with various systemic manifestations, such as cardiovascular, renal, thyroidal, gastrointestinal, and musculoskeletal disorders. Though very... -
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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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- Schizencephaly Suspected as Normal Tension Glaucoma on Ophthalmoscopic Examination
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Yoo S, Lee J
- KMID: 2125920
- J Korean Ophthalmol Soc.
- 2004 Oct;45(10):1761-1766.
PURPOSE: Occasionally, in nonglaucomatous optic atrophy, the optic nerve head may appear to be cupped to such a degree that normal tension glaucoma is suspected. We report such a case... -
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- Correlations of preoperative hormonal changes with propofol and remifentanil requirements in pituitary adenoma patients
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Kim EM, Choi EM, Choi SH, Heo SB, Min KT
- KMID: 2169223
- Anesth Pain Med.
- 2010 Apr;5(2):146-150.
BACKGROUND: Anesthetic requirements are affected by the preoperative levels of some hormones. This study investigated to identify the hormonal status such as plasma level and maximal secretary capacity correlating with... -
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- Two Cases of Kallmann Syndrome Presented with Delayed Puberty
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Choi HK, Choi JH, Yoo HW
- KMID: 2321985
- J Korean Soc Pediatr Endocrinol.
- 2005 Jun;10(1):105-109.
Kallmann syndrome is caused by the defects of migration of the olfactory and GnRH neurons from the olfactory placodes to the brain, and characterized by hypogonadotropic hypogonadism, and anosmia or... -
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- Acromegaly with Diabetes Insipidus after Pituitary Tumor Removal: Successful Pregnancy and Delivery
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Kim SH, Kim JI, Park YM, Won IS, Shin KC, Jo Y, Lee S, Kim YS, Lee KY, Park IB
- KMID: 2177862
- J Korean Endocr Soc.
- 2010 Mar;25(1):56-60.
- doi: 10.3803/jkes.2010.25.1.56
A 33-year-old woman visited our hospital because of oligomenorrhea. Acromegaly was diagnosed based on elevated insulin like growth factor-I (IGF-I) and paradoxical growth hormone (GH) rise in oral glucose tolerance... -
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- A Case of Severe Hyponatremia Associated with Hypopituitarism due to Hemorrhagic Fever with Renal Syndrome
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Jo Y, Lee S, Park J, Kim HS, Kim SH, Lee HH, Yang J, Chang JH, Chung W, Kim S
- KMID: 2307172
- Korean J Nephrol.
- 2009 Nov;28(6):624-627.
Most of the patients with hemorrhagic fever with renal syndrome (HFRS) by Hantaviruses recover completely. However, the prevalence of hypopituitarism as sequel of HFRS may be approximately 10%. However, it... -
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- Change in Endocrine Function after Treatment of Craniopharyngioma
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Lim JS, Kim SY, Yu JS, Shin CH, Yang SW
- KMID: 2001534
- J Korean Soc Pediatr Endocrinol.
- 1997 Mar;2(1):42-52.
PURPOSE:Craniopharyngioma is intracranial tumor that arises from theremnants of Rathke's pouch. Because of its location near pituitary glands and hypothalamus, many patients show endocrine dysfunction before and after surgical removal... -
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- A Case of Giant Cell Granulomatous Hypophysitis with Recurrent Hypoosmolar Hyponatremia
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Lee YH, Kim YB, Lee JH, Jeong KH, Kim MK, Song KS, Jo YS
- KMID: 1497761
- Endocrinol Metab.
- 2010 Dec;25(4):347-353.
- doi: 10.3803/EnM.2010.25.4.347
A 39-year-old woman presented with a 20 day history of recurrent hypoosmolar hyponatremia. Because her volume status seemed to be normal, the most suspected causes of her hyponatremia were adrenal... -
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- Etiologies and characteristics of children with chief complaint of short stature
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Song KC, Jin SL, Kwon AR, Chae HW, Ahn JM, Kim DH, Kim HS
- KMID: 1789529
- Ann Pediatr Endocrinol Metab.
- 2015 Mar;20(1):34-39.
- doi: 10.6065/apem.2015.20.1.34
PURPOSE: Short stature is a very common reason for visits to pediatric endocrine clinics. It could be the first sign of an underlying disease. The purpose of this study is... -
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- Genetic Analysis of Multiple Endocrine Neoplasia Type 1 (MEN1) Leads to Misdiagnosis of an Extremely Rare Presentation of Intrasellar Cavernous Hemangioma as MEN1
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Lee DM, Yu SH, Yoon HH, Lee KL, Eom YS, Lee K, Kim BJ, Kim YS, Park IB, Kim KW, Lee S
- KMID: 2169421
- Endocrinol Metab.
- 2014 Jun;29(2):146-153.
- doi: 10.3803/EnM.2014.29.2.146
BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited disorder characterized by the simultaneous occurrence of endocrine tumors in target tissues (mainly the pituitary, endocrine pancreas, and parathyroid... -
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- Complication and Prognosis of Craniopharyngioma According to the Age of Onset
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Lee EJ, Nam MS, Song YD, Lim SK, Lee HC, Huh KB, Kim KR, Song KH, Cha BS, Lee JH
- KMID: 2461571
- J Korean Soc Endocrinol.
- 1994 Sep;10(3):262-272.
Craniopharyngioma is the most common tumor involving the hypothalamo-pituitary area in childhood and adolescence. Recently, we carried out collective review of 70 patients with craniopharyngioma treated from January 1980 to... -
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