Literature DB >> 1297554

[A cervical collar therapy for non-progressive juvenile spinal muscular atrophy of the distal upper limb (Hirayama's disease)].

Y Tokumaru1, K Hirayama.   

Abstract

Non-progressive juvenile spinal muscular atrophy of the distal upper limb (Hirayama's disease) occurs predominantly in men in the second decade with unilateral weakness of the fingers and hand, and atrophy of the hand and forearm. The symptoms generally progress for 3-4 years after onset and then stop. Since the second decade is a very important period starting one's career, early stopping of the progression and possibly the improvement are essential. On the bases of the neuroradiological studies, a forward displacement of the posterior wall of the dural canal at the lower cervical level on neck flexion is presumed to be the main pathogenetic mechanism in this disease. On neck flexion, the spinal cord is compressed anteroposteriorly at C7 and C8 segmental levels. Pathological studies suggested that chronic microcirculatory disturbances in the spinal cord as the result of repeated flexion of the neck might produce necrosis of the anterior horns. We used a cervical collar for the prevention of neck flexion in 14 patients in the early stage and compared the results with those of 18 patients who had natural courses. In the therapy group, muscle weakness of the affected hand improved in 5 patients and the progression of the disease was stopped in 8 patients with the duration of 1.8 +/- 1.2 years, whereas the duration of progression of the natural course group was 2.9 +/- 1.6 years. Only one patient who could not tolerate the use of collar showed a slight progression. These results suggest that the cervical collar is a useful therapeutic tool in this disease.

Entities:  

Mesh:

Year:  1992        PMID: 1297554

Source DB:  PubMed          Journal:  Rinsho Shinkeigaku        ISSN: 0009-918X


  12 in total

1.  Hirayama disease: a frequently undiagnosed condition with simple inexpensive treatment.

Authors:  Rajesh Verma; Rakesh Lalla; Tushar B Patil; Arvind Gupta
Journal:  BMJ Case Rep       Date:  2012-12-06

2.  Hirayama Disease: Escaping From the Quotidian Imaging.

Authors:  Arjit Agarwal; Shruti Chandak; Pawan Joon
Journal:  J Clin Diagn Res       Date:  2015-08-01

Review 3.  Juvenile muscular atrophy of the distal upper extremity (Hirayama syndrome): a systematic review.

Authors:  Henrik C Bäcker; Jacob Bock; Peter Turner; Michael A Johnson; John Cunningham; Patrick Chan; Richard Gerraty
Journal:  Eur Spine J       Date:  2022-06-21       Impact factor: 3.134

4.  Hirayama disease.

Authors:  David C Kieser; P J Cox; S C J Kieser
Journal:  Eur Spine J       Date:  2018-03-14       Impact factor: 3.134

5.  Hirayama disease.

Authors:  Atul T Tayade; Sushilkumar K Kale; Arvind Pandey; Shriprakash Kalantri
Journal:  J Neurosci Rural Pract       Date:  2010-01

Review 6.  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

7.  Clinical Experiences of Uncommon Motor Neuron Disease: Hirayama Disease.

Authors:  Kyoung Hee Lee; Dae Seob Choi; Young Suk Lee; Dong Ho Kang
Journal:  Korean J Spine       Date:  2016-09-30

8.  Bimelic hirayama disease: clinical dilemma solved by imaging.

Authors:  Shalabh Jain; Siddharth Yadav; Swarna Gupta; Ritu Gupta
Journal:  Case Rep Med       Date:  2013-03-28

9.  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

10.  Hirayama's Disease - A Rare Case Report with Review of Literature.

Authors:  B S Narayana Gowda; J Mohan Kumar; Praveen Kumar Basim
Journal:  J Orthop Case Rep       Date:  2013 Jul-Sep
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