• 제목/요약/키워드: Guillain-Barr$\acute{e}$ syndrome

검색결과 37건 처리시간 0.018초

한 정신병원에서 발생한 급성 축삭성 길랑-바레 증후군으로 추정되는 환자들에 대한 임상적 연구 (A Clinical Study of Probable Acute Axonal Guillain-Barré Syndrome Occurring at a Mental Hospital)

  • 이동국
    • Annals of Clinical Neurophysiology
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    • 제2권2호
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    • pp.81-88
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    • 2000
  • 한 정신병원에 장기입원한 정신분열증환자에서 계속 발생한 8명의 급성 축삭성 GBS로 추정되는 환자들의 평균연령은 38세였으며 7명이 남자였다. 모든 환자들은 급성 상행성 양쪽하지 마비나 사지마비를 보이면서 심부 건반사가 소실되었다. 이 병은 주로 여름철에 많이 발생 하였으며 전기생리학적 검사상 축삭이 주로 손상된 소견을 보였다. IVIG치료를 한 1명을 제외한 나머지 환자들은 경제적 사정상 대증요법으로 치료하였다. AMAN형태의 환자 3명 중 1명에서 임상적 호전을 보였고, AMSAN형태의 환자 5명 중 2명에서 임상적 호전을 보였다. AMSAN형태의 환자중 1명에선 10개월 뒤 같은 증상이 재발하였다.

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항GT1a 및 항GM1강글리오시드항체 동시 양성을 보인 길랭-바레증후군과 급성파종뇌척수염의 병발 (Co-occurrence of Guillain-Barré Syndrome and Acute Disseminated Encephalomyelitis with Dual Positive of Anti-GT1a and Anti-GM1 Antibodies)

  • 이주영;유진혁;강동국;김예림;윤별아;김종국;배종석
    • 대한신경과학회지
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    • 제35권4호
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    • pp.211-214
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    • 2017
  • Acute disseminated encephalomyelitis (ADEM) and Guillain-$Barr{\acute{e}}$ syndrome (GBS) are both rare post-infectious neurological disorders. The co-existence of these conditions has often been reported despite of low incidence. We describe a 20-year-old male, who presented with acute flaccid paralysis and encephalopathy. The patient showed reversible MRI lesions suggesting ADEM. This case showed anti-GT1a IgG and anti-GM1 IgM antibodies positivity. We suggest that certain immunogenicity within central and peripheral nervous system may share a common autoimmune process during the disease course.

Clinical importance of F-waves as a prognostic factor in Guillain-Barré syndrome in children

  • Lee, Eung-Bin;Lee, Yun Young;Lee, Jae Min;Son, Su Min;Hwang, Su-Kyeong;Kwon, Soonhak;Kim, Sae Yoon
    • Clinical and Experimental Pediatrics
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    • 제59권6호
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    • pp.271-275
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    • 2016
  • Purpose: A limited number of studies have examined the link between F-wave abnormalities and clinical presentation in pediatric Guillain-$Barr{\acute{e}}$ syndrome (GBS). Therefore, this study examined the importance of F-wave abnormalities as a prognostic factor in pediatric GBS patients. Methods: The records and electrodiagnostic studies (EDS) of 70 GBS patients were retrospectively evaluated, and divided into 2 groups according to the results of EDS. Group A (n=33) presented with F-wave abnormalities, and group B (n=26) exhibited normal findings. We compared laboratory reports, clinical features, response to treatment, and prognosis between the 2 groups. Results: Motor weakness was the most frequently observed symptom for either group. Clinically, the incidence of fever and upper respiratory symptoms differed between the 2 groups, while the prevalence of abnormal deep tendon reflex (DTR) was significantly higher in group A than B (P<0.05). Patients diagnosed with GBS had received intravenous immunoglobulin treatment: 94% in group A and 58% in group B. Furthermore, significantly greater numbers of patients in group A showed H-reflex abnormalities and poor prognosis compared with group B (P<0.05). Conclusion: This study demonstrated that F-waves are a clinically important prognostic factor in GBS. F-wave abnormalities were associated with abnormal DTR and poor prognosis in patients. Limited studies have examined the link between F-wave abnormalities and clinical results; therefore, further randomized controlled studies are needed to confirm the clinical characteristics and efficacy of treatments.

Acute-onset chronic inflammatory demyelinating polyneuropathy following hepatitis A virus infection

  • Jung, Eui Sung;Kim, Ye Sel;Min, Ju-Hong;Kang, Kyusik;Lee, Jung Ju;Park, Jong-Moo;Kim, Byung-Kun;Kwon, Ohyun
    • Annals of Clinical Neurophysiology
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    • 제19권1호
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    • pp.50-53
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    • 2017
  • An infection is less likely to elicit chronic inflammatory demyelinating polyneuropathy (CIDP) than Guillain-$Barr{\acute{e}}$ syndrome. We here report a case of acute-onset CIDP following hepatitis A virus infection and briefly comment on the potential mechanisms regarding the induction and chronicity of autoimmunity after a viral infection.

Acute combined central and peripheral nervous system demyelination: a case report

  • Roh, Young Eun;Kim, Young Mi
    • 고신대학교 의과대학 학술지
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    • 제33권2호
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    • pp.257-262
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    • 2018
  • Guillain-$Barr{\acute{e}}$ syndrome (GBS) and acute disseminated encephalomyelitis (ADEM) are demyelinating neurologic disorders with different target organs. Although they share similar pathogenetic mechanism, reports of simultaneous occurrence of the 2 disorders are rare. A 2 year 6 month old girl visited our hospital for fever, cough, and general weakness. Although the muscle power of extremities showed mild weakness and voiding difficulty, initial deep tendon reflex of both knees and ankles was normal. A nerve conduction study to evaluate the weakness revealed the absence of F waves. Cerebrospinal fluid analysis demonstrated pleocytosis with lymphocyte predominance and elevated protein levels. Magnetic resonance imaging showed abnormal T2 hyperintensity in pons, medulla and spinal cord. Serum anti-GD1b antibody was positive. Based on clinical findings, laboratory findings, nerve conduction study, and neuroimaging, the diagnosis of GBS and ADEM was made. This is the first case of GBS accompanied by ADEM in Korea.

Electrognostic findings of Guillain-Barré syndrome

  • Yoon, Byeol-A;Bae, Jong Seok;Kim, Jong Kuk
    • Annals of Clinical Neurophysiology
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    • 제22권1호
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    • pp.13-18
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    • 2020
  • The electrodiagnostic findings in Guillain-Barré syndrome (GBS) play important roles in both understanding its pathophysiology and its diagnosis. Only demyelinating neuropathies were thought to be present when GBS patients were first diagnosed in Western countries, but the concept changed when many axonal GBS patients were reported in Asia. Reversible conduction failure was subsequently revealed, and it was recognized as a pathophysiologic continuum of axonal GBS. Thus, the electrodiagnostic findings in GBS have had a profound effect on the history of this disease.

Overlap syndrome of Miller-Fisher syndrome/Pharyngeal-Cervical-Brachial variant-Guillain Barre Syndrome with anti-ganglioside complex antibodies

  • Lee, Suk-yoon;Oh, Seong-il;Huh, So-Young;Shin, Kyong Jin;Kim, Jong Kuk;Yoon, Byeol-A
    • Annals of Clinical Neurophysiology
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    • 제22권2호
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    • pp.112-116
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    • 2020
  • 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.

Prevalence of virulence and cytolethal distending toxin (CDT) genes in thermophilic Campylobacter spp. from dogs and humans in Gyeongnam and Busan, Korea

  • Cho, Hyun-Ho;Kim, Sang-Hyun;Min, Wongi;Ku, Bok-Kyung;Kim, Yong-Hwan
    • 대한수의학회지
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    • 제54권1호
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    • pp.39-48
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    • 2014
  • The prevalence of thermophilic Campylobacter (C.) spp. in stray, breeding, and household dogs was 25.2, 12.0, and 8.8%, respectively. C. jejuni and C. upsaliensis were the predominant Campylobacter spp. from household dogs. cdtA, cdtB, and cdtC were detected by PCR in all isolates. Despite the high cytolethal distending toxin (CDT) gene prevalence, only 26 (31%) C. jejuni strains and one (15.3%) C. coli strain showed evidence of CDT production in HEp-2 cell cytotoxicity assays. Virulence-associated genes detected in the C. jejuni and C. coli isolates were cadF, dnaJ, flaA, racR, ciaB, iamA, pldA, virB11, ceuE, and docC. cadF, dnaJ, flaA, and ceuE were found in all C. jejuni and C. coli isolates. When detecting Guillain-Barr$\acute{e}$ syndrome-associated genes (galE, cgtB, and wlaN), galE was identified in all isolates. However, cgtB and wlaN were more prevalent in C. jejuni isolates from humans than those from dogs. Adherence and invasion abilities of the C. jejuni and C. coli strains were tested in INT-407 cells. A considerable correlation (adjusted $R^2$= 0.678) existed between adherence and invasion activities of the Campylobacter spp. isolates.

Miller Fisher syndrome in a patient with pulmonary tuberculosis

  • Park, Jae Young;Jung, Hoe Jong;Bae, Heewon;Han, Jeong-Ho;Kang, Min Ju
    • Annals of Clinical Neurophysiology
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    • 제22권2호
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    • pp.117-120
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    • 2020
  • Miller Fisher syndrome (MFS) is characterized by the acute ophthalmoparesis, ataxia and areflexia. We describe the case of 70-year-old man with cardinal symptom of MFS and active pulmonary tuberculosis (Tb). A thorough evaluation led to the diagnosis of MFS and treatment with intravenous immunoglobulin (IVIg) was started. The complete resolution of ophthalmoparesis and ataxia was observed from the fourth day of IVIg treatment. This is the first report to describe a case of MFS that developed in patient pulmonary tuberculosis.

Guillain-Barr$\acute{e}$ 증후군의 임상적 및 전기생리학적 연구 (Clinical and Electrophysiological Study on Guillain-Barr$\acute{e}$ Syndrome)

  • 윤성환;하정상;주성균;조용국;김정현;정지윤
    • Journal of Yeungnam Medical Science
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    • 제22권1호
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    • pp.52-61
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    • 2005
  • 1994년 1월부터 1999년 12월까지 6년간 영남대학교병원에 입원하여 G-B 증후군으로 진단 받은 45명의 환자를 대상으로 하여 그 임상적 양상과 신경생리학적 검사를 통한 특징을 분석 관찰하였다. 성별분포는 남자가 1.8:1로 많았고 연령은 10세 미만과 40대 연령군에서 높은 빈도를 나타내었으며 월별로는 다른 국내보고와는 달리 주로 12월과 2월 사이에 호발하였다. 선행질환은 30예 (66.7 %)에서 관찰되었고 그 중 상기도 질환이 19예로 가장 많았다. 발병당시의 임상양상은 심건반사 소실 또는 감소가 45예 (100 %), 사지 근력 약화가 38예(84.4 %)로서 두 가지 소견이 가장 많았다. 임상적 증상에 따른 정도의 차이에서는 경증이 많았으나 기관지 절개나 인공호흡이 필요하였던 경우도 10예 (22.2 %)를 보였고 입원 당시의 뇌척수액 단백세포해리 현상은 33예 (73.3 %)에서 관찰되었다. 그리고 시행된 치료로는 면역 글로불린 정맥주사가 29 예(64.4 %), 대증요법이 12예 (26.7 %)였다. 전기생리학적 진단기준 척도들 중 복합근활동전위의 진폭은 다른 기준척도에 비해 가장 초기에 현저한 변화를 보였으며, 병의 경과 중 발병 후 2~4주에 대부분의 전기생리적 기준척도가 최대 이상소견을 보였다. 그리고 임상증상과 신경생리학적 검사소견을 통한 분류에서 고전형 외에 Fisher 증후군과 축삭형을 보인경우는 각각 3예 (6.7 %)였다. 이 연구에서 G-B 증후군의 임상증상과 신경생리학적 특징은 다른 국내외 연구의 보고와 큰 차이는 없었으나 겨울철에 발생율이 높았던 점이 다른 차이였다. 그 이유에 대해서는 향후 광범위한 역학조사가 필요할 것으로 본다.

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