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A Case of Congenital Hypopituitarism with Anterior Pituitary Aplasia and Ectopic Posterior Pituitary Gland

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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Pituitary Stalk Transection Syndrome

Cho YH, Shin JH

  • KMID: 2461639
  • J Korean Soc Endocrinol.
  • 1996 Sep;11(3):324-329.
We experienced one case of severe pituitary dwarfism in a 16 years old male boy that magnetic resonance image(MRI) revealed transection of the pituitary stalk with the ectopic location of...
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Reappearance of the posterior pituitary bright signal in diabetes insipidus: MR follow-up of germinomas after radiotherapy

Lee HK, Suh DC, Chang HS

  • KMID: 2416547
  • J Korean Radiol Soc.
  • 1992 Jun;28(3):352-355.
Diabetes insipidus(DI) of central origin is a clinical syndrome resulting from low blood levels of antidiuretic hormone secreted from the posterior lobe of the pituitary gland, which is usually caused...
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A Case of Congenital Hypopituitarism with Anterior Pituitary Hypoplasia and Ectopic Posterior Pituitary Gland

Son YJ, Park HS, Shim KS, Choeh K, Han TI

  • KMID: 1829649
  • J Korean Pediatr Soc.
  • 1999 Dec;42(12):1746-1750.
The pituitary gland develops from two different parts of the brain. The anterior pituitary gland originates from the Rathke pouch and the posterior one from the infundibulum. Therefore, the pathologic...
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A Case of Delayed Puberty due to Hypoplasia of Anterior Pituitary Gland with Pituitary Stalk Agenesis and Ectopic Neurohypophysis

Shin SY, Kim JY, Yoon SJ, Kim SK, Hong SB, Kim YJ, Nam MS, Kim MR, Kim YS

  • KMID: 2199515
  • J Korean Soc Endocrinol.
  • 1999 Sep;14(3):578-586.
Hypopituitarism is not a common cause of delayed puberty, however it should always be considered, especially if there are such signs as severe dwarfism, dollish face, truncal obesity, small hands...
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A Case of Teratocarcinoma with Central Diabetes Insipidus

Kim JH, Lim IS, Choi ES, Yoo BH

  • KMID: 1654706
  • Korean J Pediatr.
  • 2004 Apr;47(4):453-457.
Central diabetes insipidus is a rare disorder that can result as a consequence of diverse etiologies, including malformations, autoimmune, infiltrative(e.g. neoplastic or histiocytosis) or traumatic processes, as well as mutations...
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Delayed diagnosis of pituitary stalk interruption syndrome with severe recurrent hyponatremia caused by adrenal insufficiency

Jang KM, Ko CW

Pituitary stalk interruption syndrome (PSIS) involves the occurrence of a thin or absent pituitary stalk, hypoplasia of the adenohypophysis, and ectopic neurohypophysis. Diagnosis is confirmed using magnetic resonance imaging. Patients...
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Primary Granulomatous Hypophysitis Presenting with Panhypopituitarism and Central Diabetes Insipidus

Oh HJ, Mok JY, Kim JE, Cho SB, Chang SA, Kim JH, Lee JM

Primary granulomatous hypophysitis is a rare inflammatory disorder of the pituitary gland and patients commonly present with symptoms of sellar compression and hypopituitarism. A 48-year-old woman was admitted due to...
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Lymphocytic infundibuloneurohypophysitis presenting with central diabetes insipidus: a case report and review of previous Korean cases

Oh SR, Cha JM, Jin AR, Park JB, Kim HY, Park BH, Cho CG

  • KMID: 2258117
  • Korean J Med.
  • 2009 Aug;77(Suppl 1):S122-S127.
Lymphocytic infundibuloneurohypophysitis is a neuroendocrine disorder characterized by autoimmune inflammation of the pituitary stalk and neurohypophysis. Clinical findings such as acute onset central diabetes insipidus and the regression of characteristic...
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Atypical Granular Cell Tumor of the Sellar Region

Rhee DJ, Choi YL, Suh YL, Park K

  • KMID: 1881637
  • J Korean Neurosurg Soc.
  • 2006 Dec;40(6):459-462.
We report a very rare case of atypical granular cell tumor arising in the neurohypophysis of a 56-year-old woman. The tumor was seen on radiology to be lobulated, soft and...
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Lymphocytic Hypophysitis: Case Report

Cho CS, Park BJ, Kim YJ, Cho MK

  • KMID: 1904550
  • J Korean Neurosurg Soc.
  • 2003 Jul;34(1):65-67.
The authors report two cases of lymphocytic hypophsitis: a 38-year-old male patient with headache and diabetes insipidus and in a 64-year-old female patient with headache. Magnetic resonance(MR) image of the...
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A Surgical Case of Lymphocytic Hypophysitis with Progressive Visual Worsening

Shin HS, Park BJ, Lim YJ

  • KMID: 2067281
  • J Korean Neurosurg Soc.
  • 2007 Sep;42(3):216-219.
Lymphocytic hypophysitis is a clinically rare disease, and it has been known to be an autoimmune disease which mainly affects pregnant women at the end of gestation or right after...
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A Case of Turner Syndrome Associated with Idiopathic Central Diabetes Insipidus

Kang B, Sung HU, Kim BK, Park SY, Kim SK, Kwon YS, Lim MK, Lee JE

We report a case of Turner syndrome associated with idiopathic central diabetes insipidus in a 12-year-old girl, who presented with polyuria and polydipsia after a year. The patient was very...
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Pituitary Irradiation by Gamma Knife in Intractable Cancer Pain

Kwon KH, Nam TK, Im YS, Lee JI

  • KMID: 1588438
  • J Korean Neurosurg Soc.
  • 2004 Oct;36(4):286-290.
OBJECTIVE: Cancer pain has been treated by gamma knife radiosurgery(GKS), targeted to the pituitary gland-stalk, as an alternative new pain control method. The purpose of this study is to prove...
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A Case of Sheehan's Syndrome Presenting Central Diabetes Insipidus

Kim DJ, Kim NH, Park JR, Yang SJ, Kim HS, Yoo HJ, Park SY, Ryu OH, Lee KW, Kim HY, Seo JA, Kim SG, Choi KM, Baik SH, Choi DS

Sheehan's syndrome occurs as a result of ischemic pituitary necrosis due to severe postpartum hemorrhage. The manifestations of this clinical syndrome are most often caused by a deficiency in the...
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A Case of Acute Toxic Encephalopathy due to an Oxycodone Overdose

Kim SP, Lee DH, Yoon DH, Kim SJ, Cho SH, Cho NS, Kim BC

  • KMID: 2332542
  • J Korean Soc Emerg Med.
  • 2008 Oct;19(5):598-601.
Acute encephalopathies can be defined as an acute central nervous system (CNS) insult, due to an underlying pathology. The clinical symptoms almost always include an acute state of confusion and...
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Severe Hyponatremia during Acyclovir Treatment in Shingles

Shin J, Kim M, Yoo JR, Kang SY, Oh JH

Acyclovir is effective in treating the herpes virus infection, especially chickenpox and shingles. Hyponatremia caused by acyclovir has been rarely reported. We present a shingles patient with symptomatic hyponatremia that...
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A Case of Pituitary Tumor Causing Diabetes Insipidus and Associating with Adenoid Cystic Carcinoma in the Bronchus

Lee KW, Hahm JR, Kang MY, Jung JH, Lee GD, Kim HJ, Chung SI

  • KMID: 2200310
  • J Korean Soc Endocrinol.
  • 2003 Jun;18(3):311-317.
The metastatic tumor occurs in about 6% to 20% of all cases with central diabetes insipidus. Many kinds of cancers such as breast, lung, colon, prostate, leukemia, and lymphoma can...
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A Case of Ectopic Neurohypophysis Presenting with Hypogonadism

Baek IW, Kim JH, Lee GJ, Lee KE, Lee HL, Lee HW, Kim NY, Ihn YK, Ko SH, Lee SH, Han JH

Pituitary stalk interruption and ectopic neurohypophysis seen on magnetic resonance Imaging (MRI) are often associated with either isolated growth hormone (GH) deficiency or combined anterior pituitary hormone deficiency, but their...
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A Case of Lymphocytic Infundibuloneurohypohysitis

Chae HB, Park JY, Shong YK, Kim KJ, Kim CH, Kwun BD, Choe GY, Hwang JB, Kim GS

  • KMID: 2251513
  • Korean J Med.
  • 1997 Mar;52(3):424-428.
Lymphocytic infundibuloneurohypphysitis(LINH) is a newly classified disorder and proposed as a common cause of idiopathic central diabetes insipidus. It is characterized by thickening of the infundibulum and/or pituitary stalk and...
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