Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

72 results
Display

A Study of Central Diabetes Insipidus in Head and Neck Langerhans Cell Histiocytosis: A Single Center Experience

Lee MJ, Park BS, Yoo YM, Jung HJ, Park JE

BACKGROUND: Langerhans cell histiocytosis (LCH) frequently involves the head and neck and increases the risk of central nervous system (CNS) involvement of LCH, such as central diabetes insipidus (CDI), when...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Central Diabetes Insipidus Linked to Rathke's Cleft Cyst, Polyuria in a 17-year-old Girl

Kim HY, Lee SJ, Bae EH, Ma SK, Kim SW

A 17-year-old girl presented with polyuria (7 L/day) and polydipsia for one year. Initial urine osmolality was 113mOsm/kg Hâ‚‚O. Following 6 h of fluid restriction, serum plasma osmolality reached 300mOsm/kg...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Neonatal Group B Streptococcal Meningitis Complicated with Secondary Hypopituitarism: A Case Report

Lee H, Lee SW, Shim SY, Park EA, Cho SJ

Group B Streptococcus (GBS) commonly causes neonatal meningitis and sepsis. In infants with late-onset meningitis, fever, irritability or lethargy or both, poor feeding, and tachypnea are common initial signs. Major...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Langerhans Cell Histiocytosis Manifested as a Suprasellar Mass

Yoon JY, Park BK, Yoo H, Lee SH, Hong EK, Park WS, Kwon YJ, Yoon JH, Park HJ

Langerhans cell histiocytosis (LCH) has diverse clinical manifestations, including intracranial mass lesions. We report a case of LCH that manifested as a suprasellar mass, and initially misdiagnosed as a germ...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Deficiency of antidiuretic hormone: a rare cause of massive polyuria after kidney transplantation

Jang KM, Sohn YS, Hwang YJ, Choi BS, Cho MH

A 15-year-old boy, who was diagnosed with Alport syndrome and end-stage renal disease, received a renal transplant from a living-related donor. On postoperative day 1, his daily urine output was...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Pulmonary Langerhans Cell Histiocytosis in an Adult Male Presenting with Central Diabetes Insipidus and Diabetes Mellitus: A Case Report

Choi YS, Lim JS, Kwon W, Jung SH, Park IH, Lee MK, Lee WY, Yong SJ, Lee SJ, Jung YR, Choi J, Choi JS, Jeong JT, Yoo JS, Kim SH

Pulmonary Langerhans cell histiocytosis is an uncommon diffuse cystic lung disease in adults. In rare cases, it can involve extrapulmonary organs and lead to endocrine abnormalities such as central diabetes...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Pituitary Granulomatosis with Polyangiitis Presenting with Central Diabetes Insipidus

Kim IY, Lee S, Kwon HJ, Lee K, Yoo KH, Cha HS, Koh EM, Lee J

We report on a case of limited form of granulomatosis with polyangiitis (GPA) with pituitary involvement which presented with central diabetes insipidus. This rare form of GPA has not been...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Primary Empty Sella Syndrome with Central Diabetes Insipidus

Han JS, Chun HW, Jo HM, Kim JH, Kim KJ, Jung CH, Mok JO, Kim CH, Kang SK, Kim BY

Primary empty sella syndrome is a phenomenon caused by cerebrospinal fluid filling resulting from the herniation of the subarachnoid space within the sella. The pituitary function of primary empty sella...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family

Kim MJ, Kim YE, Ki CS, Yoo JH

Autosomal dominant neurohypophyseal diabetes insipidus is a rare form of central diabetes insipidus that is caused by mutations in the vasopressin-neurophysin II (AVP-NPII) gene. It is characterized by persistent polydipsia...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Adult Multisystem Langerhans Cell Histiocytosis Presenting with Central Diabetes Insipidus Successfully Treated with Chemotherapy

Choi JE, Lee HR, Ohn JH, Moon MK, Park J, Lee SJ, Choi MG, Yoo HJ, Kim JH, Hong EG

We report the rare case of an adult who was diagnosed with recurrent multisystem Langerhans cell histiocytosis (LCH) involving the pituitary stalk and lung who present with central diabetes insipidus...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Septo-Optic Dysplasia Resulting in Central Diabetes Insipidus and Nonobstructive Bilateral Hydronephrosis

Kim JH, Lee KB, Lee J, Nam SM, Lee KW, Hwang EG, Gil G

A 27-year-old male with nonobstructive hydronephrosis was referred from the urology department for polyuria evaluation and management. The patient was hospitalized for urinary tract infection and cystostomy was performed due...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Syndrome of Inappropriate Scretion of Anti-Diuretic Hormone Associated with Sodium Valproate

Lee HJ, Wi JK, Moon JY, Jeong KH, Ihm CG, Lee SH, Lee TW

We report a rare case of the concurrent manifestation of central diabetes insipidus (CDI) and type 2 diabetes mellitus (DM). A 56 year-old man was diagnosed as a type 2...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Polyuria with the Concurrent manifestation of Central Diabetes Insipidus (CDI) & Type 2 Diabetes Mellitus (DM)

Shin HJ, Kim JH, Yi JH, Han SW, Kim HJ

We report a rare case of the concurrent manifestation of central diabetes insipidus (CDI) and type 2 diabetes mellitus (DM). A 56 year-old man was diagnosed as a type 2...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Morphea and Verruca Plana Complicated in Central Diabetes Insipidus

Woo YR, Lee HM, Lee JS, Koo DW

  • KMID: 2088501
  • Korean J Dermatol.
  • 2012 Oct;50(10):899-903.
Morphea, localized scleroderma, is a connective tissue disease characterized by localized, circumscribed sclerotic patches, or plaques of the skin. The pathogenesis of morphea is still unclear. Central diabetes insipidus is...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Endocrinologic Complications after Traumatic Brain Injury

Beom J, Oh BM

The endocrinologic complications such as adrenal insufficiency and hypopituitarism are common after traumatic brain injury (TBI) portending poor rehabilitation outcome. Anterior pituitary dysfunction presents as hypothyroidism, hypogonadism, growth hormone deficiency,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Transient Central Diabetes Insipidus after Aorto-Coronary Bypass Operation

Yu CH, Cho JH, Jung HY, Lim JH, Jin MK, Kwon O, Hong KD, Choi JY, Yoon SH, Kim CD, Kim YL, Kim GJ, Park SH

Diabetes insipidus (DI) is characterized by excessive urination and thirst. This disease results from inadequate output of antidiuretic hormone (ADH) from the pituitary gland or the absence of the normal...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Central Diabetes Insipidus Associated with Symptomatic Cytomegalovirus Infection in an Extremely Low Birth Weight Infant

Hong YR

I report a case of extremely low birth weight infant, who presented central diabetes insipidus associated with cytomegalovirus infection. His brain magnetic resonance imaging showed a flattened pituitary gland, and...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Unexpected Fatal Hypernatremia after Successful Cardiopulmonary Resuscitation with Therapeutic Hypothermia: A Case Report

Choi SS, Kim WY, Kim W, Lim KS

Central diabetes insipidus (DI), characterized by unexpected fatal hypernatremia, is a rare complication after successful cardiopulmonary resuscitation with therapeutic hypothermia, but may be potentially fatal if recognition is delayed. We...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Hyperglycemic Hyperosmolar Syndrome in a Patient with Central Diabetes Insipidus and Type 2 Diabetes Mellitus

Lee JH, Hong JT, Min SJ, Hong SB, Nam M, Kim YS, Kim SH

  • KMID: 2264204
  • Korean J Med.
  • 2012 Jan;82(1):90-94.
Diabetes insipidus is a disorder caused by complete or partial deficiency or unresponsiveness to antidiuretic hormone. Both diabetes mellitus and diabetes insipidus are well-known causes of polyuria and polydipsia. Although...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2022 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr