Download PDF
CC BY-NC-ND 4.0 · J Neurol Surg Rep 2018; 79(01): e19-e22
DOI: 10.1055/s-0038-1639341
Case Report
Georg Thieme Verlag KG Stuttgart · New York

Cervical Stenosis in Adult Arthrogryposis: A Case Report and Review of the Literature

Allen L. Ho
1   Department of Neurosurgery, Stanford University, Stanford, California, United States
,
Jyodi Mohole
1   Department of Neurosurgery, Stanford University, Stanford, California, United States
,
Eric S. Sussman
1   Department of Neurosurgery, Stanford University, Stanford, California, United States
,
Arjun V. Pendharkar
1   Department of Neurosurgery, Stanford University, Stanford, California, United States
,
Harminder Singh
1   Department of Neurosurgery, Stanford University, Stanford, California, United States
› Author Affiliations
Further Information

Publication History

29 August 2017

17 December 2017

Publication Date:
20 March 2018 (online)

   Permissions and Reprints

Abstract

Arthrogryposis multiplex congenita is a rare, nonprogressive congenital disorder that describes a constellation of conditions characterized by multiple joint contractures. Spinal pathology and deformity are common; however, the majority of the literature on arthrogryposis is focused on pediatric management. There exist very few reports on long-term outcomes and management of adults with arthrogryposis. We present a case of cervical spinal stenosis in an adult female with arthrogryposis that underwent posterior cervical decompression and fusion. A review of spine-related sequelae seen in adults with arthrogryposis and considerations for spinal surgery for these patients is discussed.

Keywords

Arthrogryposis - cervical stenosis - cervical fusion - congenital disorders - spinal deformity
 

  • References

  • 1 Du J, Aichmair A, Lykissas M, Girardi F. Cervical stenosis in a patient with arthrogryposis: case report. Evid Based Spine Care J 2014; 5 (01) 57-62
    PubMedGoogle Scholar
  • 2 Fletcher ND, Rathjen KE, Bush P, Ezaki M. Asymmetrical arthrogryposis of the upper extremity associated with congenital spine anomalies. J Pediatr Orthop 2010; 30 (08) 936-941
    CrossrefPubMedGoogle Scholar
  • 3 Riemer G, Steen U. Amyoplasia: a case report of an old woman. Disabil Rehabil 2013; 35 (11) 950-958
    CrossrefPubMedGoogle Scholar
  • 4 Fassier A, Wicart P, Dubousset J, Seringe R. Arthrogryposis multiplex congenita. Long-term follow-up from birth until skeletal maturity. J Child Orthop 2009; 3 (05) 383-390
    CrossrefPubMedGoogle Scholar
  • 5 Kalampokas E, Kalampokas T, Sofoudis C, Deligeoroglou E, Botsis D. Diagnosing arthrogryposis multiplex congenita: a review. ISRN Obstet Gynecol 2012; 2012: 264918
    CrossrefPubMedGoogle Scholar
  • 6 Carlson WO, Speck GJ, Vicari V, Wenger DR. Arthrogryposis multiplex congenita. A long-term follow-up study. Clin Orthop Relat Res 1985; 5 (194) 115-123
    PubMedGoogle Scholar
  • 7 Bevan WP, Hall JG, Bamshad M, Staheli LT, Jaffe KM, Song K. Arthrogryposis multiplex congenita (amyoplasia): an orthopaedic perspective. J Pediatr Orthop 2007; 27 (05) 594-600
    CrossrefPubMedGoogle Scholar
  • 8 Graydon AJ, Eastwood DM. Orthopaedic management of arthrogryposis multiplex congenita. European Surgical Orthopaedics and 2014; 4627-4644
    PubMedGoogle Scholar
  • 9 Thompson GH, Bilenker RM. Comprehensive management of arthrogryposis multiplex congenita. Clin Orthop Relat Res 1985; 5 (194) 6-14
    PubMedGoogle Scholar