The Protean Neuropsychiatric and Vestibuloauditory Manifestations of Neurosarcoidosis

被引:7
作者
Greene, Jacqueline J. [1 ]
Naumann, Ilka C. [2 ,3 ,4 ,5 ]
Poulik, Janet M. [5 ,6 ,7 ]
Nella, Kevin T. [8 ]
Weberling, Lindsay [1 ]
Harris, Jeffrey P. [9 ]
Matsuoka, Akihiro J. [1 ,10 ,11 ]
机构
[1] Northwestern Univ, Dept Otolaryngol Head & Neck Surg, Chicago, IL 60611 USA
[2] Michigan Ear Inst, Farmington Hills, MI USA
[3] Michigan State Univ, E Lansing, MI 48824 USA
[4] Oakland Univ, William Beaumont Sch Med, Rochester, MI 48063 USA
[5] Wayne State Univ, Sch Med, Detroit Med Ctr, Detroit, MI 48202 USA
[6] Wayne State Univ, Sch Med, Dept Pathol, Detroit, MI 48202 USA
[7] Childrens Hosp Michigan, Dept Pathol, Detroit, MI 48201 USA
[8] Univ Miami, Sch Med, Miami, FL USA
[9] Univ Calif San Diego, Dept Otolaryngol & Head & Neck Surg, La Jolla, CA 92093 USA
[10] Northwestern Univ, Dept Commun Sci & Disorders, Evanston, IL USA
[11] Northwestern Univ, Hugh Knowles Ctr Hearing Res, Evanston, IL USA
关键词
Neurosarcoidosis; Sarcoidosis; Cochlear implants; Cochlear implantation; Psychotic disorders; Cochlear diseases; Labyrinthine diseases; Autoimmune inner ear diseases; SUDDEN HEARING-LOSS; SARCOIDOSIS; PSYCHOSIS; DIAGNOSIS;
D O I
10.1159/000481681
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100104 ; 100213 ;
摘要
Background: A rare subset of sarcoidosis, neurosarcoidosis, is reported to occur in 5-7% of sarcoid patients and can manifest in a variety of ways. The most common are facial paralysis and optic neuritis, less commonly causing cochleovestibulopathy, blindness, anosmia, and other cranial nerve (CN) palsies. The sensory deficit may be severe and psychiatric symptoms may result from the effects of the disease or steroid treatment. Although MRI-compatible cochlear implants are now available, concerns about the feasibility of recoverable hearing with cochlear implantation in these patients as well as the practical difficulty of disease monitoring due to implant artifact must be considered. Results: We present 3 recent cases from different institutions. The first is a 39-year-old man with a history of progressively worsening hearing loss, followed by visual loss, delusions, agitation, ataxia, and musical auditory hallucinations, diffuse leptomeningeal enhancement on MRI with a normal serum angiotensin-converting enzyme (ACE) level but elevated cerebrospinal fluid (CSF) ACE levels, suggesting neurosarcoidosis, was treated with corticosteroids, and underwent successful cochlear implantation. The second is a 36-year-old woman with rapid-onset horizontal diplopia, left mixed severe sensorineural hearing loss (SNHL) and tinnitus, diffuse leptomeningeal enhancement on MRI, and progressive palsy of the left CNs IV, VI, VII, IX, X and XI, with altered mental status requiring admission following high-dose intravenous corticosteroids. The third is a 15-year-old boy who presented with sudden, bilateral, profound SNHL, recurrent headaches, and left facial weakness refractory to antivirals, ultimately diagnosed with neurosarcoidosis following an aborted cochlear implantation where diffuse inflammation was found, and histopathology revealed Schaumann bodies; he was treated with methotrexate and later underwent successful cochlear implantation. Conclusions: Neurosarcoidosis is an elusive diagnosis and can cause hearing loss and psychiatric symptoms. Cochlear implantation for patients with severe hearing loss should be considered once the diagnosis is confirmed, as it is possible to achieve a successful level of hearing. Psychiatric symptoms can manifest with the onset of neurosarcoidosis, result from CN deficits, or develop as a side effect from long-term, high-dose corticosteroids, and should be monitored carefully in patients with neurosarcoidosis. (c) 2017 S. Karger AG, Basel
引用
收藏
页码:205 / 217
页数:13
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