Literature DB >> 33709163

Neurological Complications of Endocrine Emergencies.

Salvador Cruz-Flores1.   

Abstract

PURPOSE OF REVIEW: Endocrine disorders are the result of insufficient or excessive hormonal production. The clinical course is long, and the manifestations are nonspecific due to the systemic effect of hormones across many organs and systems including the nervous system. This is a narrative review of the recent evidence of the diagnosis and treatment approach of these medical and neurological emergencies. RECENT
FINDINGS: With the possible exception of diabetic ketoacidosis, hyperosmolar hyperglycemic state, and hypoglycemia, endocrinological emergencies are complex, uncommon yet life-threatening conditions with protean and often nonspecific early clinical signs. They frequently are the first manifestation of the endocrine derangement. The systemic effects of hormones extend to the nervous system and as such, these conditions can present with neurological complications manifested, in most cases, by a diffuse dysfunction of the brain in the form of encephalopathy, delirium, seizures, and coma; or specific and peculiar syndromes such as hemichorea, hemiballism, and epilepsia partialis continua. The severity of these conditions often necessitates management in the intensive care unit requiring substantial supportive care in addition to specific targeted therapy to correct the hormonal metabolic abnormalities while at the same time blocking hormonal activity, in cases of excessive function, or supplementing hormonal deficiencies. Endocrine emergencies and their neurological complications are infrequent. The major challenge for most is early recognition. Their morbidity and mortality are high and their diagnosis requires high index of suspicion. The neurological complication most often improves with the correction of the metabolic derangement and their acuity and severity require admission to the intensive care unit.

Entities:  

Keywords:  Adrenal crisis; Diabetic ketoacidosis; Hypercalcemia; Hyperosmolar hyperglycemic state; Hypocalcemia; Myxedema; Neurological complications; Pheochromocytoma; Thyroid storm

Year:  2021        PMID: 33709163     DOI: 10.1007/s11910-021-01105-2

Source DB:  PubMed          Journal:  Curr Neurol Neurosci Rep        ISSN: 1528-4042            Impact factor:   5.081


  42 in total

1.  Pituitary apoplexy presenting as chemical meningitis.

Authors:  R Brouns; R Crols; S Engelborghs; P P De Deyn
Journal:  Lancet       Date:  2004 Aug 7-13       Impact factor: 79.321

Review 2.  Pituitary apoplexy: pathophysiology, diagnosis and management.

Authors:  Andrea Glezer; Marcello D Bronstein
Journal:  Arch Endocrinol Metab       Date:  2015-06       Impact factor: 2.309

3.  Pituitary Apoplexy With Bilateral Oculomotor Nerve Palsy.

Authors:  Sevan R Komshian; Ramin Saket; Khamid Bakhadirov
Journal:  Neurohospitalist       Date:  2018-05-07

4.  Pituitary apoplexy: large surgical series with grading system.

Authors:  David H Jho; Beverly M K Biller; Pankaj K Agarwalla; Brooke Swearingen
Journal:  World Neurosurg       Date:  2014-06-08       Impact factor: 2.104

5.  Pituitary apoplexy: a review of clinical presentation, management and outcome in 45 cases.

Authors:  Latika Sibal; Steve G Ball; Vincent Connolly; Robert A James; Philip Kane; William F Kelly; Pat Kendall-Taylor; David Mathias; Petros Perros; Richard Quinton; Bijay Vaidya
Journal:  Pituitary       Date:  2004       Impact factor: 4.107

6.  Pituitary Apoplexy: Results of Surgical and Conservative Management Clinical Series and Review of the Literature.

Authors:  Joao Paulo Almeida; Miguel Marigil Sanchez; Claire Karekezi; Nebras Warsi; Rodrigo Fernández-Gajardo; Jyoti Panwar; Alireza Mansouri; Suganth Suppiah; Farshad Nassiri; Romina Nejad; Walter Kucharczyk; Rowena Ridout; Andrei F Joaquim; Fred Gentili; Gelareh Zadeh
Journal:  World Neurosurg       Date:  2019-07-11       Impact factor: 2.104

Review 7.  Natural history of nonfunctioning pituitary adenomas and incidentalomas: a systematic review and metaanalysis.

Authors:  M Mercè Fernández-Balsells; Mohammad Hassan Murad; Amelia Barwise; Juan F Gallegos-Orozco; Anu Paul; Melanie A Lane; Julianna F Lampropulos; Inés Natividad; Lilisbeth Perestelo-Pérez; Paula G Ponce de León-Lovatón; Patricia J Erwin; Jantey Carey; Victor M Montori
Journal:  J Clin Endocrinol Metab       Date:  2011-04       Impact factor: 5.958

8.  Pituitary apoplexy masquerading as meningoencephalitis.

Authors:  Davinder S Jassal; Gregory McGinn; John M Embil
Journal:  Headache       Date:  2004-01       Impact factor: 5.887

Review 9.  Pituitary Apoplexy.

Authors:  Claire Briet; Sylvie Salenave; Jean-François Bonneville; Edward R Laws; Philippe Chanson
Journal:  Endocr Rev       Date:  2015-09-28       Impact factor: 19.871

10.  Pituitary apoplexy: an update on clinical and imaging features.

Authors:  Alessandro Boellis; Alberto di Napoli; Andrea Romano; Alessandro Bozzao
Journal:  Insights Imaging       Date:  2014-10-16
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  1 in total

1.  Deficiency of Thyroid Hormone Reduces Voltage-Gated Na+ Currents as Well as Expression of Na+/K+-ATPase in the Mouse Hippocampus.

Authors:  Sivaraj Mohana Sundaram; Romy Marx; Heiko M Lesslich; Irmgard D Dietzel
Journal:  Int J Mol Sci       Date:  2022-04-08       Impact factor: 6.208

  1 in total

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