Literature DB >> 20300781

Camptocormia: the bent spine syndrome, an update.

Thibaut Lenoir1, Nathalie Guedj, Philippe Boulu, Pierre Guigui, Michel Benoist.   

Abstract

Camptocormia, also referred to as bent spine syndrome (BSS) is defined as an abnormal flexion of the trunk, appearing in standing position, increasing during walking and abating in supine position. BSS was initially considered, especially in wartime, as a psychogenic disorder. It is now recognized that in addition to psychiatric syndromes, many cases of reducible BSS have a somatic origin related to a number of musculo-skeletal or neurological disorders. The majority of BSS of muscular origin is related to a primary idiopathic axial myopathy of late onset, appearing progressively in elderly patients. Diagnosis of axial myopathy first described by Laroche et al. is based upon CT/MRI examination demonstrating massive fatty infiltration of paravertebral muscles. The non-specific histological aspect includes an extensive endomysial fibrosis and fat tissue with irregular degenerated fibers. Weakness of the paravertebral muscles can be secondary to a wide variety of diseases generating diffuse pathologic changes in the muscular tissue. BSS can be the predominant and sometimes revealing symptom of a more generalized muscular disorder. Causes of secondary BSS are numerous. They must be carefully assessed and ruled out before considering the diagnosis of primary axial myopathy. The principal etiologies include on the one hand inflammatory myopathies, muscular dystrophies of late onset, myotonic myopathies, endocrine and metabolic myopathies, and on the other hand neurological disorders, principally Parkinson's disease. Camptocormia in Parkinsonism is caused by axial dystonia, which is the hallmark of Parkinson's disease. There is no specific pharmacologic treatment for primary axial myopathy. General activity, walking with a cane, physiotherapy, and exercises should be encouraged. Treatment of secondary forms of BSS is dependent upon the variety of the disorder generating the muscular pathology. Pharmacologic and general management of camptocormia in Parkinson's disease merge with that of Parkinsonism. Levodopa treatment, usually active on tumor rigidity and akinesia, has poor or negative effect on BSS.

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Year:  2010        PMID: 20300781      PMCID: PMC2989190          DOI: 10.1007/s00586-010-1370-5

Source DB:  PubMed          Journal:  Eur Spine J        ISSN: 0940-6719            Impact factor:   3.134


  38 in total

1.  Camptocormia as a form of dystonia in Parkinson's disease.

Authors:  J Sławek; M Derejko; P Lass
Journal:  Eur J Neurol       Date:  2003-01       Impact factor: 6.089

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3.  Parkinson's disease with camptocormia.

Authors:  F Bloch; J L Houeto; S Tezenas du Montcel; F Bonneville; F Etchepare; M L Welter; S Rivaud-Pechoux; V Hahn-Barma; T Maisonobe; C Behar; J Y Lazennec; E Kurys; I Arnulf; A M Bonnet; Y Agid
Journal:  J Neurol Neurosurg Psychiatry       Date:  2006-06-05       Impact factor: 10.154

4.  Injection of the iliopsoas muscle with botulinum toxin in camptocormia.

Authors:  Carlo Colosimo; Filippo Maria Salvatori
Journal:  Mov Disord       Date:  2009-01-30       Impact factor: 10.338

5.  A specific clinical pattern of camptocormia in Parkinson's disease.

Authors:  A-C Lepoutre; D Devos; A Blanchard-Dauphin; V Pardessus; C-A Maurage; D Ferriby; J-F Hurtevent; A Cotten; A Destée; L Defebvre
Journal:  J Neurol Neurosurg Psychiatry       Date:  2006-05-30       Impact factor: 10.154

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7.  [Camptocormia: a sign of axial myopathy. Report of 7 cases].

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Journal:  Rev Med Interne       Date:  2002-02       Impact factor: 0.728

8.  Localised nodular myositis: a clinical and pathological variant of polymyositis.

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9.  Axial myopathy--an unrecognised entity.

Authors:  Ibrahim Mahjneh; G Marconi; A Paetau; A Saarinen; T Salmi; H Somer
Journal:  J Neurol       Date:  2002-06       Impact factor: 4.849

10.  Is camptocormia a primary muscular disease?

Authors:  M Laroche; M B Delisle; R Aziza; J Lagarrigue; B Mazieres
Journal:  Spine (Phila Pa 1976)       Date:  1995-05-01       Impact factor: 3.468

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  14 in total

1.  Camptocormia as an onset symptom of myasthenia gravis.

Authors:  Toko Sato; Takahiro Natori; Takanori Hata; Nobuo Yamashiro; Kazumasa Shindo; Yoshihisa Takiyama
Journal:  Neurol Sci       Date:  2016-11-03       Impact factor: 3.307

2.  Rigid Spine Syndrome among Children in Oman.

Authors:  Roshan Koul; Dilip Sankhla; Suad Al-Jahdhami; Renjith Mani; Rana A Rahim; Saif Al-Yaarubi; Hussein Al-Kindy; Khalid Al-Thihli; Amna Al-Futaisi
Journal:  Sultan Qaboos Univ Med J       Date:  2015-08-24

3.  [Causes of camptocormia].

Authors:  F X Glocker; U G Berninger
Journal:  Nervenarzt       Date:  2013-08       Impact factor: 1.214

Review 4.  Anterocollis and camptocormia in parkinsonism: a current assessment.

Authors:  Gonzalo J Revuelta
Journal:  Curr Neurol Neurosci Rep       Date:  2012-08       Impact factor: 5.081

5.  A novel late-onset axial myopathy associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene.

Authors:  Sissel Løseth; Nicol C Voermans; Torberg Torbergsen; Sue Lillis; Christoffer Jonsrud; Sigurd Lindal; Erik-Jan Kamsteeg; Martin Lammens; Marcus Broman; Gabriele Dekomien; Paul Maddison; Francesco Muntoni; Caroline Sewry; Aleksandar Radunovic; Marianne de Visser; Volker Straub; Baziel van Engelen; Heinz Jungbluth
Journal:  J Neurol       Date:  2013-01-18       Impact factor: 4.849

6.  Whole-body muscle MRI to detect myopathies in non-extrapyramidal bent spine syndrome.

Authors:  Mickaël Ohana; Marie-Christine Durand; Catherine Marty; Jean-Philippe Lazareth; Thierry Maisonobe; Dominique Mompoint; Robert-Yves Carlier
Journal:  Skeletal Radiol       Date:  2014-05-31       Impact factor: 2.199

Review 7.  Therapy-resistant symptoms in Parkinson's disease.

Authors:  Ruxandra Julia Vorovenci; Roberta Biundo; Angelo Antonini
Journal:  J Neural Transm (Vienna)       Date:  2015-09-26       Impact factor: 3.575

Review 8.  Neuromuscular issues in systemic disease.

Authors:  Wolfgang Grisold; Anna Grisold
Journal:  Curr Neurol Neurosci Rep       Date:  2015-07       Impact factor: 6.030

Review 9.  Bent spine syndrome as an initial manifestation of late-onset multiple acyl-CoA dehydrogenase deficiency: a case report and literature review.

Authors:  Yufen Peng; Min Zhu; Junjun Zheng; Yuanzhao Zhu; Xiaobing Li; Caixia Wei; Daojun Hong
Journal:  BMC Neurol       Date:  2015-07-24       Impact factor: 2.474

10.  Axial mitochondrial myopathy in a patient with rapidly progressive adult-onset scoliosis.

Authors:  Annie Hiniker; Lee-Jun Wong; Sigurd Berven; Cavatina K Truong; Adekunle M Adesina; Marta Margeta
Journal:  Acta Neuropathol Commun       Date:  2014-09-16       Impact factor: 7.801

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