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"Hearing loss"

Case Reports
A Long-Term Follow-up of Pontine Hemorrhage With Hearing Loss
Seung Ki Kim, Ae Ryoung Kim, Joon Yeop Kim, Deog Young Kim
Ann Rehabil Med 2015;39(4):634-639.   Published online August 25, 2015
DOI: https://doi.org/10.5535/arm.2015.39.4.634

A pontine intracranial hemorrhage (ICH) evokes several neurological symptoms, due to the various nuclei and nerve fibers; however, hearing loss from a pontine ICH is rare. We have experienced a non-traumatic pontine ICH patient, with hearing loss. A 43-year-old male patient had a massive pontine hemorrhage; his brain magnetic resonance imaging revealed the hemorrhage on the bilateral dorsal pons, with the involvement of the trapezoid body. Also, profound hearing loss on the pure-tone audiogram and abnormal brainstem auditory evoked potential were noticed. Fifty-two months of long-term follow-up did not reveal any definite improvement on the patient's hearing ability.

Citations

Citations to this article as recorded by  
  • Bilateral Hearing Loss and Tinnitus as Primary Manifestations of Pontine Hemorrhage in a Young Man With Refractory Hypertension
    Zhuo Luan, Aleksandr Drozdov, Jithendhar Kandimalla
    Cureus.2025;[Epub]     CrossRef
  • Mild Traumatic Brain Injury and the Auditory System: An Overview of the Mechanisms, Clinical Presentations, and Current Diagnostic Modalities
    Mark Harris, Andrew Nguyen, Nolan J. Brown, Bryce Picton, Julian Gendreau, Nicholas Bui, Ronald Sahyouni, Harrison W. Lin
    Journal of Neurotrauma.2024; 41(13-14): 1524.     CrossRef
  • Determination risk factors for severe and profound hearing loss in child candidates for cochlear implantation in southeast of Iran during 2014-2020
    Parya Jangipour Afshar, Jila Afsharmanesh, Marzieh Eslahi, Hojjat Sheikhbardsiri, Mahmood Nekoei Moghadam
    BMC Pediatrics.2022;[Epub]     CrossRef
  • Management of Primary Brainstem Hemorrhage: A Review of Outcome Prediction, Surgical Treatment, and Animal Model
    Peng Chen, Haijun Yao, Xiaoyong Tang, Yanglingxi Wang, Qingtao Zhang, Yang Liu, Jin Hu, Yongbing Deng, Zhongjie Shi
    Disease Markers.2022; 2022: 1.     CrossRef
  • Case report: Near-complete cortical hearing loss caused by sequential development of bilateral putaminal hemorrhage
    Yoshito Arakaki, Takeshi Yoshimoto, Hiroyuki Ishiyama, Tomotaka Tanaka, Yorito Hattori, Masafumi Ihara
    eNeurologicalSci.2022; 29: 100431.     CrossRef
  • Surgical management of temporal lobe intracerebral hemorrhage presenting with bilateral deafness: a case report
    Doyoung Na, Hyukjai Choi, Yongjun Cho, Jinpyeong Jeon
    Journal of the Korean Society of Stereotactic and Functional Neurosurgery.2021; 17(1): 30.     CrossRef
  • Primary Brainstem Hemorrhage: A Review of Prognostic Factors and Surgical Management
    Danyang Chen, Yingxin Tang, Hao Nie, Ping Zhang, Wenzhi Wang, Qiang Dong, Guofeng Wu, Mengzhou Xue, Yuping Tang, Wenjie Liu, Chao Pan, Zhouping Tang
    Frontiers in Neurology.2021;[Epub]     CrossRef
  • Acute onset bilateral hearing loss in dorsomedial pontine hemorrhage
    Masashi Hoshino, Hisanao Akiyama, Satoru Kashima, Kaima Soga, Takahiro Shimizu, Yasuhiro Hasegawa
    Medicine.2019; 98(34): e16902.     CrossRef
  • 7,911 View
  • 64 Download
  • 5 Web of Science
  • 8 Crossref
Churg-Strauss Syndrome Presented With Hearing Impairment and Facial Palsy
Jeong-Hyun Byun, Jong-Hoo Lee, In-Sung Choi
Ann Rehabil Med 2014;38(6):852-855.   Published online December 24, 2014
DOI: https://doi.org/10.5535/arm.2014.38.6.852

Churg-Strauss syndrome (CSS) is a rare systemic necrotizing vasculitis. Cranial nerve involvement is very rare in CSS. A 59-year-old woman had complained of both hearing impairments for eight months and left facial palsy for three months. Left facial and cochlear neuropathies were detected in electrodiagnostic studies. Paranasal sinus computed tomography (CT) showed chronic pansinusitis. Chest CT revealed eosinophilic infiltration in the right upper lobe. Tissue biopsy of the right inferior turbinate displayed necrotizing vasculitis with eosinophilic infiltration. She was diagnosed as CSS, based on the presence of eosinophilia, pulmonary infiltration, paranasal sinusitis, and biopsy containing blood vessels with extravascular eosinophils. She was treated with intravenous and oral steroids and azathioprine, showing relatively good prognosis on facial palsy and hearing impairment. We report a very rare case of CSS presented with hearing impairment and facial palsy.

Citations

Citations to this article as recorded by  
  • Prognostic Factors Affecting Hearing in Otitis Media With ANCA-Associated Vasculitis Patients: A Systematic Review and Meta-Analysis
    Chen Li, Mengyao Xie, Zhiyuan Wu, Shu Wang, Zhijin Han, Qi Tang, Ruoyan Xue, Yongli Zhang, Hua Yang
    Ear, Nose & Throat Journal.2023;[Epub]     CrossRef
  • Clinical characteristics, the diagnostic criteria and management recommendation of otitis media with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (OMAAV) proposed by Japan Otological Society
    Yasuaki Harabuchi, Kan Kishibe, Kaori Tateyama, Yuka Morita, Naohiro Yoshida, Masahiro Okada, Yasuomi Kunimoto, Takeshi Watanabe, Akira Inagaki, Tadao Yoshida, Mitsuyoshi Imaizumi, Takeshi Nakamura, Takeshi Matsunobu, Shigeto Kobayashi, Yukiko Iino, Shing
    Auris Nasus Larynx.2021; 48(1): 2.     CrossRef
  • Facial nerve palsy in giant-cell arteritis: case-based review
    Eveline Claeys, Olivier Gheysens, Wouter Meersseman, Eric Verbeken, Daniel Blockmans, Liesbet Henckaerts
    Rheumatology International.2021; 41(2): 481.     CrossRef
  • Conjunctival Eosinophilic Granulomatosis With Polyangiitis (Churg-Strauss) in a Young Adult Male With Persistent Ptosis
    Luke C. Olson, Gary J. Lelli, Sarju S. Patel, Cynthia M. Magro
    JCR: Journal of Clinical Rheumatology.2021; 27(2): e53.     CrossRef
  • Characteristics of and Prognosis for Facial Palsy in Patients With Otitis Media With ANCA-Associated Vasculitis (OMAAV)
    Keishi Fujiwara, Shinya Morita, Atsushi Fukuda, Hiroko Yanagi, Kimiko Hoshino, Yuji Nakamaru, Yasushi Furuta, Akihiro Homma
    Otology & Neurotology.2021; 42(10): e1577.     CrossRef
  • Clinical features and treatment outcomes of otitis media with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (OMAAV): A retrospective analysis of 235 patients from a nationwide survey in Japan
    Yasuaki Harabuchi, Kan Kishibe, Kaori Tateyama, Yuka Morita, Naohiro Yoshida, Yasuomi Kunimoto, Takamichi Matsui, Hiroshi Sakaguchi, Masahiro Okada, Takeshi Watanabe, Akira Inagaki, Shigeto Kobayashi, Yukiko Iino, Shingo Murakami, Haruo Takahashi, Tetsuya
    Modern Rheumatology.2017; 27(1): 87.     CrossRef
  • Head and Neck Manifestations of Eosinophilic Granulomatosis with Polyangiitis
    Jared M. Goldfarb, Mindy R. Rabinowitz, Shristi Basnyat, Gurston G. Nyquist, Marc R. Rosen
    Otolaryngology–Head and Neck Surgery.2016; 155(5): 771.     CrossRef
  • Otologic Manifestations in Patients with ANCA Associated Vasculitis-Comparative Analysis among Microscopic Polyangiitis, Granulomatosis with Polyangiitis and Eosinophilic Granulomatosis with Polyangiitis
    Yoshiyuki Kawashima, Yoshihiro Noguchi, Taku Ito, Kota Mizushima, Masatoki Takahashi, Ken Kitamura, Takeshi Tsutsumi
    Nippon Jibiinkoka Gakkai Kaiho.2016; 119(2): 110.     CrossRef
  • Focus on audiologic impairment in eosinophilic granulomatosis with polyangiitis
    Veronica Seccia, Susanna Fortunato, Lodovica Cristofani‐Mencacci, Iacopo Dallan, Augusto P. Casani, Manuela Latorre, Pierluigi Paggiaro, Maria Laura Bartoli, Stefano Sellari‐Franceschini, Chiara Baldini
    The Laryngoscope.2016; 126(12): 2792.     CrossRef
  • 5,350 View
  • 35 Download
  • 8 Web of Science
  • 9 Crossref
A Case of De Novo 18p Deletion Syndrome with SensorineuralHearing Loss: A case report.
Kim, Seung Hwan , Hong, Ji Yoen , Yim, Shin Young
J Korean Acad Rehabil Med 2008;32(5):591-594.
Chromosome 18p deletion syndrome is one of the most frequent autosomal abnormalities with more than 150 reported cases in the world and 7 reported cases in South Korea. Frequent clinical features of 18p deletion syndrome include intellectual disability, growth retardation, and dysmorphic features including ptosis. To the best of our knowledge, sensorineural hearing loss has not been reported in the 18p deletion syndrome until now. A case with sensorineural hearing impairment associated with hypoplasia of bilateral cochlear nerves is presented in this paper. The sensorineural hearing impairment seen in this case could be related with deleted gene(s) located in the short arm of chromosome 18 or be an independent feature unrelated with 18p deletion. Further case reports are required in order to better define the relation between sensorineural hearing loss and the 18p deletion syndrome. (J Korean Acad Rehab Med 2008; 32: 591-594)
  • 1,813 View
  • 11 Download
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