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Polychondritis presenting with oculomotor and abducens nerve palsies as the initial manifestation
Mitsuhiro Akiyama1, Yuko Kaneko1, Hironari Hanaoka1
1a Division of Rheumatology, Department of Internal Medicine , Keio University School of Medicine , Tokyo , Japan.
Abstract:
We treated a patient with relapsing polychondritis (RP) who presented with intermittent oculomotor and abducens nerve palsies as the first manifestation. Ear swelling and laryngeal edema emerged 7 months later, which led us to diagnose him with RP. Moderate doses of glucocorticoid resolved all symptoms. Our experience with RP accompanied by oculomotor nerve palsy suggests that RP should be considered in patients with cranial nerve palsies so that they may be promptly diagnosed and treated.
Insights
Relapsing polychondritis (RP) can initially manifest as cranial nerve palsies, specifically oculomotor and abducens nerve issues. Early diagnosis and glucocorticoid treatment are crucial for managing this rare autoimmune condition.
Area of Science:
- Rheumatology and Neurology
- Autoimmune and Inflammatory Diseases
Background:
- Relapsing polychondritis (RP) is a rare, systemic autoimmune disorder characterized by progressive destruction of cartilaginous tissues.
- Cranial nerve palsies, while uncommon, can be a presenting feature of RP, potentially delaying diagnosis.
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