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"So-Young Huh"

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"So-Young Huh"

Case Reports

Autonomic instability in severe tetanus: a case report
Seung Won Seo, Jaewon Lee, Bong-Goo Yoo, Jehun Kim, So-Young Huh
Ann Clin Neurophysiol 2021;23(2):117-120.   Published online October 29, 2021
DOI: https://doi.org/10.14253/acn.2021.23.2.117
Tetanus is an infectious disease of the nervous system caused by Clostridium tetani, and is characterized by tonic muscle contractions, painful spasms, and autonomic dysfunction. Severe autonomic dysfunction associated with tetanus can be life-threatening. We present a 62-year-old female who experienced lockjaw after an ankle fracture. The patient was diagnosed with tetanus and received tetanus immunoglobulin and a vaccination. The patient subsequently experienced labile hypertension. This case highlights the challenge and importance of managing cardiovascular instability.

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Citations to this article as recorded by  
  • Successful management of severe generalized tetanus in a 23‐year man with phenobarbital adjuvant: A case report
    Arezoo Ahmadi, Elahe Karimpour‐Razkenari, Ramin Ansari, Mahforouzalsadat Marashi, Hamidreza Sharifnia, Atabak Najafi, Mojtaba Mojtahedzadeh
    Clinical Case Reports.2023;[Epub]     CrossRef
  • 8,470 View
  • 188 Download
  • 1 Crossref
Overlap syndrome of Miller-Fisher syndrome/Pharyngeal-Cervical-Brachial variant-Guillain Barre Syndrome with anti-ganglioside complex antibodies
Suk-yoon Lee, Seong-il Oh, So-Young Huh, Kyong Jin Shin, Jong Kuk Kim, Byeol-A Yoon
Ann Clin Neurophysiol 2020;22(2):112-116.   Published online October 28, 2020
DOI: https://doi.org/10.14253/acn.2020.22.2.112
Guillain-Barré syndrome (GBS) and Miller Fisher syndrome (MFS) can present with overlapping features. A 56-year-old female developed ptosis and diplopia after an upper respiratory infection, and presented with facial palsy, dysarthria, brachial weakness, ataxia, and areflexia. Mild weakness of both legs appeared after a few days. Anti-ganglioside complex antibody were positive to IgG GM1/GQ1b and GQ1b/sulfatide antibodies. The present case suggests that the manifestation of overlap between MFS/PCB variants and GBS could be caused by antiganglioside complex antibodies.

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  • Overlap of Miller-Fisher Syndrome and Pharyngeal-Cervical-Brachial Variant Secondary to COVID-19 in Recurrent Guillain-Barré Syndrome: A Case Report
    Tarek Hammad, Sayeed Hossain, Amin Alayyan
    Cureus.2024;[Epub]     CrossRef
  • 7,666 View
  • 149 Download
  • 1 Crossref
Steroid-resistant sarcoid myositis that was successfully treated with oral methotrexate
Kyung-Ha Noh, So-Young Huh, Young-Eun Park, Jin-Hong Shin, Dae-Seong Kim
Ann Clin Neurophysiol 2020;22(1):41-45.   Published online April 30, 2020
DOI: https://doi.org/10.14253/acn.2020.22.1.41
Acute sarcoid myositis is rarely complicated by sarcoidosis, and steroid therapy is considered the standard treatment. We experienced a patient with acute sarcoid myositis who did not respond to aggressive high-dose corticosteroid therapy, but showed a dramatic improvement after the addition of weekly low-dose oral methotrexate (MTX). This intervention allowed the resumption of normal daily activities after 6 months. Our case strongly suggests that MTX should be considered in patients with acute sarcoid myositis that is resistant to corticosteroid therapy.
  • 4,331 View
  • 114 Download

Brief Communication

Congenital Myotonic Dystrophy Pathologically MimickingX-Linked Myotubular Myopathy
Jin-Sung Park, So-Young Huh, Na-Yeon Jung, Jin-Hong Shin
J Korean Soc Clin Neurophysiol 2012;14(2):80-82.
  • 1,963 View
  • 10 Download
Chronic Inflammatory Demyelinating PolyneuropathyAssociated with HIV-Infection
So-Young Huh, Bo-Young Ahn, Se-Jin Oh, Yeong-Eun Park, Dae-Seong Kim
J Korean Soc Clin Neurophysiol 2011;13(2):97-100.
Chronic inflammatory demyelinating polyneuropathy (CIDP) is an acquired immune-mediated polyneuropathy. Corticosteroids,intravenous immunoglobulin (IVIG) and plasmapheresis have been reported to be effective treatment. Rarely, CIDP can occurin the patients with HIV infection. The clinical features and electrophysiological findings of CIDP are known to be similarin patients with and without HIV infection. We report a 30-year-old male with HIV infection associated CIDP who improvedafter the administration of intravenous immunoglobulin and long term oral prednisone.
  • 2,457 View
  • 30 Download
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