Abstract

IntroductionWe report the case of a patient with Churg-Strauss syndrome with eighth cranial nerve palsy. Vestibulocochlear nerve palsy is extremely rare in Churg-Strauss syndrome. To the best of our knowledge, only one case of complicated neuropathy of the eighth cranial nerve has been described in a previous report presenting an aggregate calculation, but no differentiation between polyarteritis nodosa and Churg-Strauss syndrome was made. High-dose immunoglobulin was administered to our patient, and her neuropathy of the eighth cranial nerve showed improvement.Case presentationAt the age of 46, a Japanese woman developed Churg-Strauss syndrome that later became stable with low-dose prednisolone treatment. At the age of 52, she developed sudden difficulty of hearing in her left ear, persistent severe rotary vertigo, and mononeuritis multiplex. At admission, bilateral perceptive deafness of about 80dB and eosinophilia of 4123/μL in peripheral blood were found. A diagnosis of cranial neuropathy of the eighth cranial nerve associated with exacerbated Churg-Strauss syndrome was made. Although high doses of steroid therapy alleviated the inflammatory symptoms and markers, the vertigo and bilateral hearing loss remained. Addition of a high-dose immunoglobulin finally resulted in marked alleviation of the symptoms associated with neuropathy of the eighth cranial nerve.ConclusionsA high dose of immunoglobulin therapy shows favorable effects in neuropathy of the eighth cranial nerve, but no reports regarding its efficacy in cranial neuropathy have been published.

Highlights

  • We report the case of a patient with Churg-Strauss syndrome with eighth cranial nerve palsy

  • A high dose of immunoglobulin therapy shows favorable effects in neuropathy of the eighth cranial nerve, but no reports regarding its efficacy in cranial neuropathy have been published

  • intravenous immunoglobulin (IVIg) shows favorable effects in neuropathy of the peripheral nerves, no reports regarding its efficacy in cranial neuropathy have been published

Read more

Summary

Conclusions

Guillevin et al [9] reported that only four out of 96 CSS cases were complicated by cranial neuropathy. The perceptive deafness with vertigo corresponded to pathological conditions of CSS, such as increased MPO-ANCA and some inflammatory markers and exacerbated neuropathy of the peripheral nerves. As for mononeuritis multiplex of the sensory nerves, mPSL pulse therapy was effective. IVIg could possibly be a useful treatment for cranial neuropathy associated with CSS and should be taken into consideration for cases in which the effects of mPSL pulse therapy are insufficient or administration of immunosuppressants is difficult.

Introduction
Discussion
15. Dalakas MC
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call