Results 11 to 20 of about 27,042 (184)

Masked diabetes insipidus in pituitary metastasis from breast cancer after thalamic biopsy: a case report

Journal of Medical Case Reports, 2022
Background Symptomatic pituitary metastasis is rare; furthermore, it can result in diabetes insipidus and panhypopituitarism. Since diabetes insipidus is masked by concurrent panhypopituitarism, it can impede the diagnosis of pituitary dysfunction.
Hiroaki Hashimoto, Tomoyuki Maruo, Masami Nakamura, Yukitaka Ushio, Masayuki Hirata, Haruhiko Kishima   +5 more
doaj   +1 more source

Pengelolaan Central Diabetes Insipidus Pasca Cedera Kepala Berat

Jurnal Neuroanestesi Indonesia, 2019
Cedera otak traumatika adalah salah satu penyebab kematian dan kesakitan tersering pada kelompok masyarakat muda. Hasil akhir dari cedera kepala berat dapat menyebabkan gangguan kognitif, perilaku, psikologi dan sosial. Salah satu konsekuensi dari cedera
Bona Akhmad Fithrah, Marsudi Rasman, Siti Chasnak Saleh   +2 more
doaj   +1 more source

Idiopathic partial central diabetes insipidus

Einstein (São Paulo), 2023
Diabetes insipidus is a rare disorder characterized by the inability to concentrate urine, which results in hypotonic urine and increased urinary volume.
Larissa Fabre, Viviane Calice da Silva
doaj   +1 more source

Diabetes Insipidus In Patients With Traumatic Severe Brain Injury

Qanun Medika: Jurnal Kedokteran Fakultas Kedokteran Universitas Muhammadiyah Surabaya, 2019
Traumatic severe brain injury is a fatal injury, with a mortality rate of up to 50%. About 1.5 million people experience severe brain injury in the United States. There are more than 50,000 deaths and 500,000 incidents of permanent neurological sequelae.
Yudha Adi Prabowo, Prananda Surya Airlangga   +1 more
doaj   +1 more source

Acute myeloid leukemia with hypothalamic involvement causing central diabetes insipidus [PDF]

, 2018
Not ...
Duran, M., Ertürk, M.S., Ufuk, Furkan
core   +2 more sources

Prevalence of various forms of diabetes insipidus and its complications in the Republic of Uzbekistan

Mìžnarodnij Endokrinologìčnij Žurnal, 2020
Background. Central diabetes insipidus is characte­rized by the inability of the kidneys to reabsorb water and concentrate urine, which is due to the defect in the synthesis or secretion of vasopressin and is manifested by severe thirst and excretion of ...
Yu.M. Urmanova, D.I. Khamraeva
doaj   +1 more source

Radiotherapy in langerhans cell histiocytosis : a rare indication in a rare disease [PDF]

, 2013
Introduction: Langerhans Cell Histiocytosis (LCH) represents a rare benign disorder, previously designated as "Histiocytosis X", "Type II Histiocytosis" or "Langerhans Cell Granulomatosis".
Bruns, Frank, Büntzel, Jens, Eich, Hans Theodor, Haverkamp, Uwe, Heyd, Reinhard, Kriz, Jan, Micke, Oliver, Schäfer, Ulrich, Seegenschmiedt, Heinrich   +8 more
core   +1 more source

DIABETES INSIPIDUS: LITTLE-KNOWN FACTS

Исследования и практика в медицине, 2019
The most common causes of diabetes insipidus are neurosurgical operations on the pituitary gland due to its defeat by benign and malignant tumors, the neoplasms themselves, lymphocytic hypophysitis.
L. Yu. Morgunov
doaj   +1 more source

Sarcoidosis of the hypothalamus and pituitary stalk [PDF]

, 1992
We report a rare case of sarcoidosis of the hypothalamic and suprasellar region, with clinical course and the magnetic resonance imaging follow ...
BE Kendall, BJ Stern, Claudia Vogl, CN Linden, DL Veseley, Joachim Stemmler, Josef Lissner, LD Reed, M Brant-Zawadzki, MV Spagnoli, P Delaney, Peter C. Scriba, Thomas J. Voglt, W Ricker, WC Wiederholt, WS Hayes   +15 more
core   +1 more source

Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family [PDF]

Annals of Pediatric Endocrinology & Metabolism, 2014
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.
Myo-Jing Kim, Young-Eun Kim, Chang-Seok Ki, Jae-Ho Yoo   +3 more
doaj   +1 more source