Related Experiment Video
Updated: Aug 8, 2026

09:44
Neuro-rehabilitation Approach for Sudden Sensorineural Hearing Loss
Published on: January 25, 2016
[Horton's disease and corticosteroid-responsive hearing loss]
D Saadoun1, P Cacoub, N Costedoat-Chalumeau
1Service de Médecine Interne, Groupe Hospitalier Pitié-Salpêtrière, 75651 Paris Cedex 13.
Summary
Sudden hearing loss can be an early sign of temporal arteritis (TA), a large artery inflammation. Prompt treatment of TA may improve hearing in over half of affected patients.
Area of Science:
- Rheumatology
- Otolaryngology
- Neurology
Background:
- Temporal arteritis (TA), an inflammatory panarteritis affecting large arteries, typically occurs in the elderly.
- While often presenting with classic symptoms, 5-10% of TA patients exhibit nonclassical manifestations.
- Hearing loss is a rare but significant nonclassical presentation of TA.
Observation:
- Two new cases of sudden, bilateral, and corticosteroid-responsive hearing loss associated with TA are presented.
- In one case, hearing loss preceded the diagnosis of temporal arteritis.
- Literature review identified 18 previously reported cases of TA and deafness.
Findings:
- Sensorineural hearing loss can be the initial presenting symptom of temporal arteritis.
- The mechanism of deafness in TA is likely due to vertebrobasilar or cochleovestibular arteritis.
- Diagnosis of TA can be challenging, particularly when hearing loss is the sole or primary symptom.
Implications:
- Early recognition of sensorineural hearing loss as a potential TA symptom is crucial.
- Prompt diagnosis and treatment of TA may lead to partial or complete hearing recovery in 55% of cases.
- This highlights the importance of considering TA in elderly patients with unexplained hearing loss.
More Related Videos
Related Concept Videos
Adrenal Gland Disorders
Adrenal gland disorders manifest when the production of adrenal hormones deviates from the norm, resulting in either excessive or insufficient concentrations.
Adrenal insufficiency, characterized by insufficient cortisol and aldosterone production, leads to conditions like Addison's disease. This disorder, affecting the adrenal cortex, exhibits symptoms such as skin bronzing, dehydration, low blood pressure, fatigue, and weight loss. Congenital adrenal hyperplasia, a genetic ailment causing...
Adrenal insufficiency, characterized by insufficient cortisol and aldosterone production, leads to conditions like Addison's disease. This disorder, affecting the adrenal cortex, exhibits symptoms such as skin bronzing, dehydration, low blood pressure, fatigue, and weight loss. Congenital adrenal hyperplasia, a genetic ailment causing...
Antiasthma Drugs: Inhaled Corticosteroids and Glucocorticoids
Inhaled corticosteroids (ICS) are anti-inflammatory drugs used primarily in treating persistent asthma and providing long-term maintenance. They target the bronchial mucosa, the lining of the airways, to control inflammation, a critical factor in asthma progression and exacerbation.
ICS work through a multifaceted mechanism of action. They suppress the inflammatory response caused by the proliferation of TH cells. They also reduce the transcription of the IL-2 gene, which is involved in the...
ICS work through a multifaceted mechanism of action. They suppress the inflammatory response caused by the proliferation of TH cells. They also reduce the transcription of the IL-2 gene, which is involved in the...
Drug Toxicity: Allergic Reactions
Drug-related allergies are immune-mediated responses triggered by the administration of pharmacological agents. These hypersensitivity reactions are classified based on the immune mechanisms involved. The four primary types—Type I, II, III, and IV—are mediated by different immunological pathways and exhibit distinct clinical manifestations.Type I Hypersensitivity/ IgE-Mediated Reactions: Immunoglobulin E (IgE) immediately mediates Type I hypersensitivity reactions. Upon initial exposure to a...
Graves' Disease I: Introduction
Graves' disease is an autoimmune disorder that causes hyperthyroidism, or overactivity of the thyroid gland. It results from autoantibodies called thyroid-stimulating immunoglobulins (TSIs), which bind to thyroid-stimulating hormone (TSH) receptors, leading to overstimulation of hormone production and a hypermetabolic state.EtiologyAlthough considered idiopathic, Graves’ disease has well-established contributing factors. There is a strong genetic component, with increased prevalence in...
Cushing Syndrome I: Introduction
Cushing syndrome refers to the collection of clinical manifestations that arise when tissues are exposed to excessive amounts of cortisol or cortisol-like medications over an extended period. Cortisol, a glucocorticoid produced by the adrenal cortex, regulates metabolism, immune responses, and the body’s adaptation to stress. When its concentration remains chronically elevated, these physiological pathways become dysregulated, resulting in the characteristic features of the syndrome.Exogenous...
Cushing Syndrome II: Pathophysiology
Cortisol production is normally governed by the hypothalamic–pituitary–adrenal (HPA) axis, which maintains hormonal balance through tightly regulated feedback mechanisms. Disruption of this regulatory system is central to the development of Cushing syndrome, whether the excess cortisol originates from external medications or internal pathology. Persistent cortisol elevation alters metabolism, immune function, and endocrine signaling, producing the characteristic clinical features of the...

