Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Aug 18;66(3):329-335.
doi: 10.5606/tftrd.2020.4527. eCollection 2020 Sep.

The rate of intraspinal problems and clinical evaluation of scoliosis: A cross-sectional, descriptive study

Affiliations

The rate of intraspinal problems and clinical evaluation of scoliosis: A cross-sectional, descriptive study

Filiz Tuna et al. Turk J Phys Med Rehabil. .

Abstract

Objectives: This study aims to define the chronological, angular, and topographic classes in presumed idiopathic scoliosis and to investigate the frequency of generalized joint hypermobility, pain, neurological deficit, ankle deformity, Risser grade, and magnetic resonance imaging (MRI) findings in these patients.

Patients and methods: This cross-sectional, descriptive study included a total of 36 patients (11 males, 25 females; mean age 13.4±4.6 years; range, 6 to 24 years) with idiopathic scoliosis between January 2015 and January 2019. Data including age, sex, complaint of pain, generalized joint hypermobility (based on Beighton score), neurological deficit, ankle deformity, and definition of scoliosis were recorded. Chronological, angular, and topographic classification were carried out. The Risser grade and MRI findings were noted.

Results: Of all patients, 30 (83.3%) were idiopathic, five (13.9%) were neuromuscular, and one (2.8%) was congenital scoliosis based on MRI findings. Of 13 (36.1%) spine MRI scans, six (46.2%) were intraspinal anomalies, four were syringomyelia (30.8%), one was Chiari type 1 malformation (7.7%), and one was hemivertebrae with diastematomyelia (7.7%). The highest rates of classes according to chronological, angular, and topographical classifications of idiopathic scoliosis were adolescent (17/30, 56.7%), low angular (24/30, 80.0%), and lumbar scoliosis (15/30, 50.0%), respectively. Ten patients (33.3%) complained of pain, while 23 patients (76.7%) had no neurological deficit and seven (23.3%) had hypoesthesia. Seventeen patients (56.7%) had generalized joint hypermobility.

Conclusion: Idiopathic scoliosis with non-severe spinal deformity may present with intraspinal neural axis abnormalities, even when it is neurologically intact. Based on our study results, it seems to be useful to consider whole spine MRI for the evaluation of thoracic and lumbar scoliosis.

Keywords: Chiari; hypermobility; scoliosis; spine; syringomyelia.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest: The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.

Figures

Figure 1
Figure 1. An 11-year-old female with presumed idiopathic scoliosis (left lumbar) in the absence of neurological findings. Syringomyelia was detected based on whole spine magnetic resonance imaging. Finally, neuromuscular scoliosis was defined. (a) An aesthetic profile of trunk of patient affected by spinal deformities. (b) The trunk forward bending test (Adam’s forward test). (c) Cobb angle.
Figure 2
Figure 2. Chiari malformation in 19-year-old female with presumed idiopathic scoliosis (right thoracic) diagnosed using whole spine magnetic resonance imaging (level of brainstem to sacrum). Finally, neuromuscular scoliosis was defined.
Figure 3
Figure 3. A 12-year-old male with presumed idiopathic scoliosis (left lumbar) in the absence of neurological findings. (a) An aesthetic profile of trunk of patient affected by spinal deformities. (b) A frontal radiographic study. (c) Magnetic resonance imaging evaluation showing diastematomyelia at the level of Th10-Th11 intervertebral discs (the spinal cord is divided longitudinally into two parts by a fibrous septum). Finally, congenital scoliosis was defined.

Similar articles

Cited by

References

    1. Kleinberg S. The operative treatment of scoliosis. Arch Surg. 1922;5:631–645.
    1. Grivas TB, Wade MH, Negrini S, O’Brien JP, Maruyama T, Hawes MC, et al. SOSORT consensus paper: school screening for scoliosis. Where are we today. Scoliosis. 2007;2:17–17. - PMC - PubMed
    1. Negrini S, Donzelli S, Aulisa AG, Czaprowski D, Schreiber S, de Mauroy JC, et al. 2016 SOSORT guidelines: orthopaedic and rehabilitation treatment of idiopathic scoliosis during growth. Scoliosis Spinal Disord. 2018;13:3–3. - PMC - PubMed
    1. Yılmaz H, Zateri C, Kusvuran Ozkan A, Kayalar G, Berk H. Prevalence of adolescent idiopathic scoliosis in Turkey: an epidemiological study. Spine J. 2020;20:947–955. - PubMed
    1. Weinstein SL, Dolan LA, Spratt KF, Peterson KK, Spoonamore MJ, Ponseti IV. Health and function of patients with untreated idiopathic scoliosis: a 50-year natural history study. JAMA. 2003;289:559–567. - PubMed

LinkOut - more resources