Skip to main content
Log in

Camptocormia: the bent spine syndrome, an update

  • Review Article
  • Published:
European Spine Journal Aims and scope Submit manuscript

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.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. Ashour R, Jankovic J (2006) Joint and skeletal deformities in Parkinson’s disease, multiple system atrophy and progressive supranuclear palsy. Mov Disord 21:1856–1863

    Article  PubMed  Google Scholar 

  2. Azher SN, Jankovic J (2005) Camptocormia: pathogenesis, classification and response to therapy. Neurology 65:355–359

    Article  PubMed  Google Scholar 

  3. Bloch F, Houeto JL, Tezena du Montcel S et al (2006) Parkinson’s disease with camptocormia. J Neurol Neurosurg Psychiatry 77:1223–1228

    Article  CAS  PubMed  Google Scholar 

  4. Bouchaud-Chabot A, Sicre J, Bardin Th, Kahn MF (1996). Myosites focales. In: Kahn MF, Kuntz et al (eds) L’actualité rhumatologique. Expansion scientifique Française. pp 55–64

  5. Bulke JA, Crolla D, Termote JL et al (1981) Computed tomography of the muscles. Muscle Nerve 4:67–72

    Article  Google Scholar 

  6. Charpentier P, Dauphin A, Stojkovic T et al (2005) Maladie de Parkinson, camptocormie et myosite focale paraspinale. Rev. Neurol. 161:459–463

    Article  CAS  PubMed  Google Scholar 

  7. Cumming W, Weiser R, Teoh R et al (1977) Localized nodular myositis: a clinical and pathological variant of polymyositis. Q J Med 46:531–546

    CAS  PubMed  Google Scholar 

  8. Delcey V, Hachulla E, Michon-Pasturel U et al (2002) La camptocormie: un signe de myopathie axiale. A propos de sept observations. Rev Med Interne 23:144–154

    Article  CAS  PubMed  Google Scholar 

  9. Dietz V, Zylstra W, Assaiante C et al (1993) Balance control in Parkinson disease. Gait Posture 1:77–84

    Article  Google Scholar 

  10. Djaldetti R, Mosber G, Galili R, Sroka H et al (1999) Camptocormia in patients with Parkinson’s disease: characterization and possible pathogenesis of an unusual phenomenon. Mov Disord 14:443–447

    Article  CAS  PubMed  Google Scholar 

  11. Ehrenstein MR, Stoll T, Edwards JCW (1996) Not all stoops are due to osteoporosis. Ann Rhum Dis 55:21–28

    Article  CAS  Google Scholar 

  12. Emery AEH (1998) The muscular dystrophies. BMJ 317:991–995

    CAS  PubMed  Google Scholar 

  13. Heffner R, Armbrustmacher V, Eanle K (1977) Focal myositis. Cancer 40:301–306

    Article  PubMed  Google Scholar 

  14. Hilliquin P, Menkes CJ, Laoussadi S et al (1992) Camptocormie du sujet âgé: Une nouvelle entité par atteinte des muscles paravertébraux. Rev Rhum Mal Osteoartic 59:169–175

    CAS  PubMed  Google Scholar 

  15. Hund E, Heckl R, Goebel H et al (1995) Inclusion body myositis presenting with isolated erected spinal paresis. Neurology 45:993–994

    CAS  PubMed  Google Scholar 

  16. Hurst AF (1918) The bent back of soldiers. BMJ 2:621–623

    Article  Google Scholar 

  17. Jankovic J, Tintner R (2001) Dystonia and Parkinsonism. Parkinson Dis Relat Disord 8:109–121

    Article  CAS  Google Scholar 

  18. Karkowski K (1999) The old and new camptocormia. Spine 24:1494–1498

    Article  Google Scholar 

  19. Laroche M, Curtas P (2008) Usefullness of CT scan in bent spine syndrome (personnal communication)

  20. Laroche M, Delisle MB (1994) La camptocormie primitive est une myopathie para-vertébrale. Rev Rhum Mal osteoartic 61:481–484

    CAS  Google Scholar 

  21. Laroche M, Delisle MB, Aziza R et al (1995) Is camptocormia a primary muscular disease? Spine 20:1011–1016

    Article  CAS  PubMed  Google Scholar 

  22. Laroche M, Delisle MB, Mazieres B et al (1991) Myopathic localisée aux muscles spinaux: une cause de cyphose lombaire acquise de l’adulte. Rev Rhum Mal osteoartic 58:829–838

    CAS  PubMed  Google Scholar 

  23. Laroche M, Ricq G, Delisle MB (2002) Bent spine syndrome: computed tomography study and isokinetic evaluation. Muscle Nerve 25:189–193

    Article  PubMed  Google Scholar 

  24. Laroche M, Rousseau H, Mazieres B et al (1989) Intérêt de la tomodensitométrie dans la pathologie musculaire. Rev Rhum Mal Osteoartic 56:433–439

    CAS  PubMed  Google Scholar 

  25. Lepoutre AC, Devos D, Blanchard-Dauphin A (2006) A specific clinical pattern of camptocormia in Parkinson’s disease. J Neurol Neurosurg Psychiatry 77:1229–1234

    Article  PubMed  Google Scholar 

  26. Mahjneh I, Marconi G, Paetau A et al (2002) Axial myopathy—an unrecognized entity. J Neurol 249:730–734

    Article  PubMed  Google Scholar 

  27. Nieves AV, Miyasaki JM, Lang AE (2001) Acute onset dystonic camptocormia caused by lenticular lesions. Mov Disord 16:177–180

    Article  CAS  PubMed  Google Scholar 

  28. Poullin P, Daumen-Legre V, Serratrice G (1993) Camptocormie du sujet âgé. Rev Rhum Mal Osteoartic 60:159–1661

    CAS  Google Scholar 

  29. Reichel G, Kirchhofer U, Stenner A (2001) Camptocormia-segmental dystonia. Proposal of a new definition for an old disease. Nervenarzt 72:281–285

    Article  CAS  PubMed  Google Scholar 

  30. Ricker K, Koch MC, Lehmann-Horn F et al (1995) Proximal myotonic myopathy. Clinical features of a multisystem disorder similar to myotonic dystrophy. Arch Neurol 52:25–31

    CAS  PubMed  Google Scholar 

  31. Ricq G, Laroche M (2000) Cyphose lombaire acquise de l’adulte par myopathie primitive des muscles paravertébraux. Aspects épidémiologiques tomodensitométriques et évolutifs. A propos d’une cohorte de 23 patients. Rev Rhum Mal Osteoartic 67:908–913

    Article  Google Scholar 

  32. Rolland Y, Laroche M (1997) Cyphoses lombaires acquises révélatrices d’une maladie de Steinert. Rachis 9:115–118

    Google Scholar 

  33. Salvatori FM (2009) Injection of the iliopsoas muscle with botulinum toxin in camptocormia. Mov Disord 24:316

    PubMed  Google Scholar 

  34. Sandler SA (1947) Camptocormia or the functional bent back. Psychosomat Med 9:197–204

    CAS  Google Scholar 

  35. Schabitz WR, Glatz K, Schuhan C et al (2003) Severe flexion forward of the trunk in Parkinson’s disease: focal myopathy of the paraspinal muscles mimicking camptocormia. Mov Disord 18:408–414

    Article  PubMed  Google Scholar 

  36. Serratrice G, Poujet J, Pelissier JF (1996) Bent spine syndrome. J Neurol Neurosurg Psychiatry 60:51–54

    Article  CAS  PubMed  Google Scholar 

  37. Serratrice J, Weiler PJ, Pouget J, Serratrice G (2000) Une cause méconnue de camptocormie: la myopathie myotonique proximale. Presse Med 29:1121–1123

    CAS  PubMed  Google Scholar 

  38. Serratrice G, Pelissier JF, Cros J (1978) Les atteintes musculaires des osteomalacies. Rev Rhum Mal Osteoartic 45:621–630

    CAS  PubMed  Google Scholar 

  39. Slawek J, Derejko M, Lass P (2003) Camptocormia as a form of dystonia in Parkinson’s disease. Eur J Neurol 10:107–108

    Article  CAS  PubMed  Google Scholar 

  40. Souques A (1914–1915) Contractures ou pseudo-contractures hystero-traumatiques. Rev Neurol 28:430–431

    Google Scholar 

  41. Souques A, Rosanoff-Saloff B (1914–1915). La camptocormie, incurvation du tronc, consecutive aux traumatismes du tronc et des lombes, considérations morphologiques. Rev Neurol 28:937–939

    Google Scholar 

  42. Tiple D, Fabbrini G, Ottaviani D et al (2009) Camptocormia in Parkinson’s disease: an epidemiological and clinical study. J Neurol Neurosurg Psychiatry 80:145–148

    Article  CAS  PubMed  Google Scholar 

  43. Von Coelin R, Raible A, Gasser T et al (2008) Ultrasound-guided injection of the iliopsoas muscle with botulinum toxin in camptocormia. Mov Disord 23:889–892

    Article  Google Scholar 

  44. Wunderlich S, Csoti I, Bliners K et al (2002) Camptocormia in Parkinson’s disease mimicked by focal myositis of the paraspinal muscles. Mov Disord 17:598–600

    Article  PubMed  Google Scholar 

  45. Yamada K, Goto S, Matsuzaki K et al (2006) Alleviation of camptocormia by bilateral subthalamic nucleus stimulation in a patient with Parkinson’s disease. Parkinsonism Relat Disord 12(6):372–375

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

We would like to thank Maryse Lesage for her excellent secretarial work.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Nathalie Guedj.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lenoir, T., Guedj, N., Boulu, P. et al. Camptocormia: the bent spine syndrome, an update. Eur Spine J 19, 1229–1237 (2010). https://doi.org/10.1007/s00586-010-1370-5

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00586-010-1370-5

Keywords

Navigation