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Hirayama disease/cervical flexion-induced myelopathy progressing to spastic paraparesis: A report on three cases with literature review.
Preethish-Kumar, Veeramani; Polavarapu, Kiran; Nashi, Saraswati; Bhattacharya, Kajari; Saini, Jitender; Vengalil, Seena; Pruthi, Nupur; Bhat, Dhananjay I; Nalini, Atchayaram.
Afiliação
  • Preethish-Kumar V; Department of Neurology; Department of Clinical Neurosciences, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.
  • Polavarapu K; Department of Neurology; Department of Clinical Neurosciences, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.
  • Nashi S; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.
  • Bhattacharya K; Department of Neuro Imaging and Interventional Radiology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.
  • Saini J; Department of Neuro Imaging and Interventional Radiology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.
  • Vengalil S; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.
  • Pruthi N; Department of Neurosurgery, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.
  • Bhat DI; Department of Neurosurgery, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.
  • Nalini A; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.
Neurol India ; 66(4): 1094-1099, 2018.
Article em En | MEDLINE | ID: mdl-30038100
ABSTRACT
Hirayama disease (HD)/cervical flexion-induced myelopathy (CFIM) is a lower motor neuron disease conventionally affecting a single upper extremity. We describe three men progressing after a long stable period to develop severe spastic paraparesis and bladder disturbances as a protracted implication of HD. The age at onset was 20, 24, and 15 years, while the age at presentation was 27, 41, and 57 years, respectively. The second phase of disease progression occurred after 4, 13, and 28 years of stationary period. All had CFIM with characteristic magnetic resonance imaging features as observed during progressive stages. The anterior dural shift extended variably from C4 to D4 levels with a median value of 5 mm and was maximum at C6 to C7 levels, pushing the cord anteriorly causing compression. This study emphasizes the need to recognize this unusual subgroup of HD and mandates long-term follow-up with timely intervention in arresting the progression/improving the deficits.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofias Musculares Espinais da Infância / Paraparesia Espástica Tipo de estudo: Systematic_reviews Limite: Adolescent / Adult / Humans / Male / Middle aged Idioma: En Revista: Neurol India Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Índia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofias Musculares Espinais da Infância / Paraparesia Espástica Tipo de estudo: Systematic_reviews Limite: Adolescent / Adult / Humans / Male / Middle aged Idioma: En Revista: Neurol India Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Índia