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Updated: Apr 20, 2026

Neuro-rehabilitation Approach for Sudden Sensorineural Hearing Loss
Published on: January 25, 2016
Relapsing polychondritis with severe hearing loss
Francisco Vileimar Andrade de Azevedo1, Juliana de Deus E Albuquerque1, Deborah Pereira Gonçalves1
1Hospital Geral Dr. Waldemar Alcântara, Fortaleza, CE, Brasil.
Relapsing polychondritis (RP) can cause severe hearing loss, particularly when linked with systemic vasculitis. Early diagnosis and treatment are crucial for managing this rare immune-mediated condition.
Area of Science:
- Rheumatology
- Immunology
- Otolaryngology
Background:
- Relapsing polychondritis (RP) is a rare immune-mediated disorder affecting cartilaginous and proteoglycan-rich tissues.
- It commonly involves the ears, nose, joints, and respiratory tract, but can also affect eyes, heart, and inner ear structures.
- RP is associated with other conditions, including vasculitis, connective tissue diseases, and myelodysplastic syndrome, in about one-third of cases.
Observation:
- Inner ear disorders are prevalent in 40-50% of RP patients, though profound hearing loss is infrequent.
- This case study details a patient with relapsing polychondritis presenting with severe bilateral hearing loss.
- The patient also exhibited clinical signs of systemic vasculitis.
Findings:
- The co-occurrence of relapsing polychondritis, severe bilateral hearing loss, and systemic vasculitis highlights a severe disease manifestation.
- This specific case underscores the potential for RP to lead to significant auditory impairment.
- The association with systemic vasculitis suggests a complex interplay of autoimmune processes.
Implications:
- Early diagnosis and prompt treatment are vital for patients presenting with severe RP manifestations, such as profound hearing loss.
- Recognizing the link between RP and systemic vasculitis is important for comprehensive patient management.
- This case emphasizes the need for multidisciplinary care involving rheumatologists, otolaryngologists, and audiologists.
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