Results 11 to 20 of about 17,906 (224)
Frontiers in Oncology, 2022 Immune checkpoint inhibitors have improved the survival in patients affected by an increasing number of malignancies, but they may also trigger various autoimmune side-effects, including endocrinopathies.
Agnese Barnabei +8 more
doaj +1 more source
Otolaryngology Case Reports, 2020 We present a rare case of transient central diabetes insipidus occurring in the setting of endoscopic sinus surgery, without evidence of structural intracranial/pituitary complications. Other etiologic factors were excluded.
Muhammad Ansar +4 more
doaj +1 more source
Pituitary macroadenoma: A case of balanced deficiencies
Journal of Clinical and Translational Endocrinology Case Reports, 2021 Introduction: We present a patient with a non-functional pituitary macroadenoma who developed diabetes insipidus after initiation of thyroid hormone and cortisol replacement for central hypothyroidism and adrenal insufficiency.
Robert D. Leimbach +2 more
doaj +1 more source
Clinical Case Reports, 2022 This paper aims to introduce a patient with Chiari type 1 malformation presented with upper extremity pain and diabetes insipidus. After laboratory examinations, we confirmed our case's central diabetes insipidus diagnosis.
Faramarz Roohollahi +3 more
doaj +1 more source
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
A novel detrimental homozygous mutation in the WFS1 gene in two sisters from nonconsanguineous parents with untreated diabetes insipidus [PDF]
, 2019 Given the limited lifespan and with the recent progress in experimental treatments for WS, timely diagnosis and multidisciplinary treatment for DI/DM, hydronephrosis, and visual/psychiatric status-maintaining quality of life-are of crucial ...
Delides, Alexandros +11 more
core +2 more sources
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 +8 more
core +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
Endocrinology, Diabetes & Metabolism Case Reports, 2018 The combination of hyperosmolar hyperglycaemic state and central diabetes insipidus is unusual and poses unique diagnostic and therapeutic challenges for clinicians.
Snezana Burmazovic +3 more
doaj +1 more source
Thunderclap headache caused by a pituitary non-functioning tumour presenting as spontaneous pituitary apoplexy [PDF]
Romanian Journal of Neurology, 2009 Hemorrhagic or ischemic pituitary apoplexy is a rare neuro-endocrine emergency, potentially leading to coma. Neuro-ophthalmic symptoms or complications are amongst the most prevalent clinical features at onset, especially in previously asymptomatic ...
Carmen Georgescu +5 more
doaj +1 more source