Literature DB >> 2494847

MR Imaging of the cervical cord in juvenile amyotrophy of distal upper extremity.

A Biondi1, D Dormont, I Weitzner, P Bouche, P Chaine, J Bories.   

Abstract

We report the MR studies of the cervical cord in seven patients presenting juvenile muscular atrophy of distal upper extremity. This illness, also known as monomelic amyotrophy or benign focal amyotrophy, is distinct from the other motor neuron diseases. Seen in young males, it is characterized by muscular atrophy of the hand, and usually of the forearm, most often unilateral. The underlying process, of unknown origin, affects the anterior horn cells in the lower cervical cord. The gradual onset of purely motor disturbances may mimic early amyotrophic lateral sclerosis. This latter diagnosis may be excluded because of clinical stabilization and lack of pyramidal tract involvement. In our series, five MR studies were positive. In three cases we were able to demonstrate focal and unilateral atrophy in the lower cervical cord limited to the anterior horn region. Morphologic MR findings correlated with clinical and electromyographic features. In two other cases the MR-clinical correlation was more complex. No pathologic MR signal was detected on either T1- or T2-weighted images. Although the diagnosis of monomelic muscular atrophy is based on neurologic and neurophysiologic data, MR provides confirmatory evidence as well as useful information contributing to an understanding of this disease.

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Year:  1989        PMID: 2494847      PMCID: PMC8331379     

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  14 in total

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2.  A predominantly cervical form of spinal muscular atrophy.

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3.  Cardiovascular and sudomotor dysfunction in Hirayama disease.

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5.  Juvenile distal spinal muscular atrophy of upper extremities in Chinese males: a single fibre electromyographic study of arms and legs.

Authors:  Y W Chan; R Kay; M S Schwartz
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-02       Impact factor: 10.154

6.  Lack of cervical paraspinal muscle involvement in juvenile distal spinal muscular atrophy: an electromyographic study on 15 cases.

Authors:  K P Kao; K P Lin; C M Chern; Z A Wu; C P Tsai; K K Liao
Journal:  J Neurol       Date:  1993-05       Impact factor: 4.849

7.  Amyotrophic cervical myelopathy in adolescence.

Authors:  S Toma; Z Shiozawa
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8.  Hirayama disease in a 17-year-old Chinese man.

Authors:  C M Sitt; L W Fung; H Y Yuen; A T Ahuja
Journal:  Singapore Med J       Date:  2014-06       Impact factor: 1.858

Review 9.  Nosology of juvenile muscular atrophy of distal upper extremity: from monomelic amyotrophy to Hirayama disease--Indian perspective.

Authors:  Kaukab Maqbool Hassan; Hirdesh Sahni
Journal:  Biomed Res Int       Date:  2013-08-26       Impact factor: 3.411

10.  Clinical and radiological profile of Hirayama disease: A flexion myelopathy due to tight cervical dural canal amenable to collar therapy.

Authors:  K M Hassan; Hirdesh Sahni; Atul Jha
Journal:  Ann Indian Acad Neurol       Date:  2012-04       Impact factor: 1.383

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