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      KCI등재후보

      지방흡입술 이후 발생한 양측 상완 신경총 손상으로 나타난 압박마비유전신경병 - 증례보고 = Hereditary Neuropathy with Liability to Pressure Palsies Presenting with Bilateral Brachial Plexopathy after Liposuction - Case Report

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      https://www.riss.kr/link?id=A104502826

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      다국어 초록 (Multilingual Abstract)

      Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal dominant disorder characterized by recurrent entrapment neuropathies following an episode of compression or trauma. Reports on bilateral brachial plexopathy of HNPP are ra...

      Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal dominant disorder characterized by recurrent entrapment neuropathies following an episode of compression or trauma. Reports on bilateral brachial plexopathy of HNPP are rare. We report on a case of a 21-year-old female patient with no past medical history, who presented with sudden paralysis and hypoesthesia of bilateral upper extremities after undergoing liposuction. Clinical and electrodiagnostic tests were consistent with brachial plexopathy. Genetic study for the peripheral myelin protein-22 (PMP22) gene confirmed the diagnosis of HNPP presenting with bilateral brachial plexopathy. This case indicates that HNPP should be suspected in patients with brachial plexopathy when it develops after pressure-leading events such as a minor surgical procedure.

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      참고문헌 (Reference)

      1 Russo M, "Variable phenotypes are associated with PMP22 missense mutations" 21 : 106-114, 2011

      2 Li J, "The PMP22 gene and its related diseases" 47 : 673-698, 2013

      3 Shy ME, "T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy" 59 : 358-364, 2006

      4 Mouton P, "Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion" 52 : 1440-1446, 1999

      5 van Paassen BW, "PMP22 related neuropathies: Charcot-marie-tooth disease type 1A and hereditary neuropathy with liability to pressure palsies" 9 : 38-, 2014

      6 Topakian R, "Hereditary neuropathy with liability to pressure palsies presenting with sciatic neuropathy" 2014

      7 Infante J, "Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion" 24 : 1149-1155, 2001

      8 Kim KE, "Characteristic features of hereditary neuropathy with liability to pressure palsy (HNPP) presenting with brachial plexopathy in soldiers" 346 : 174-177, 2014

      9 Orstavik K, "Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies" 24 : 1093-1096, 2001

      10 Bulusu S, "A report of hereditary neuropathy with liability to pressure palsy (HNPP) presenting with brachial plexopathy: The value of complete electrodiagnostic testing" 51 : 183-190, 2011

      1 Russo M, "Variable phenotypes are associated with PMP22 missense mutations" 21 : 106-114, 2011

      2 Li J, "The PMP22 gene and its related diseases" 47 : 673-698, 2013

      3 Shy ME, "T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy" 59 : 358-364, 2006

      4 Mouton P, "Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion" 52 : 1440-1446, 1999

      5 van Paassen BW, "PMP22 related neuropathies: Charcot-marie-tooth disease type 1A and hereditary neuropathy with liability to pressure palsies" 9 : 38-, 2014

      6 Topakian R, "Hereditary neuropathy with liability to pressure palsies presenting with sciatic neuropathy" 2014

      7 Infante J, "Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion" 24 : 1149-1155, 2001

      8 Kim KE, "Characteristic features of hereditary neuropathy with liability to pressure palsy (HNPP) presenting with brachial plexopathy in soldiers" 346 : 174-177, 2014

      9 Orstavik K, "Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies" 24 : 1093-1096, 2001

      10 Bulusu S, "A report of hereditary neuropathy with liability to pressure palsy (HNPP) presenting with brachial plexopathy: The value of complete electrodiagnostic testing" 51 : 183-190, 2011

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2020-07-01 학술지명변경 외국어명 : Jouranl of Korean Association of EMG Electrodiagnostic Medicine -> Journal of Electrodiagnosis and Neuromuscular Diseases KCI등재
      2018-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2016-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      2015-12-01 평가 등재후보 탈락 (기타)
      2013-01-01 평가 등재후보학술지 유지 (기타) KCI등재후보
      2012-01-01 평가 등재후보학술지 유지 (기타) KCI등재후보
      2011-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2010-01-01 평가 등재후보 1차 FAIL (등재후보1차) KCI등재후보
      2008-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0 0 0.02
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.01 0.03 0.249 0
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