Spinal Manifestations of Systemic Disease

https://doi.org/10.1016/j.rcl.2018.10.005Get rights and content

Section snippets

Key points

  • Identifying the predominant pattern of disease (musculoskeletal system vs nervous system) helps generate an appropriate differential diagnosis.

  • Radiologists must thoroughly review the electronic medical record and prior imaging (including nonspine imaging) to add specificity to the differential diagnosis.

  • CT and MR imaging are often complementary in assessment of spinal manifestations of system disease.

Normal anatomy and imaging techniques

Spinal involvement in systemic disease is markedly varied but often disease-specific, which may include bones, synovial joints, intervertebral disks, paraspinal soft tissue, epidural space, meninges, or spinal cord. Thus, interpreting radiologists must be familiar with spinal anatomy. Identifying the space of origin of a spinal lesion (intradural extramedullary, prevertebral, osseous, and so forth.) may help generate a succinct, appropriate differential diagnosis. Additionally, it is critical

Imaging protocols

A 1-size-fits-all approach to imaging protocols may not be optimal when approaching potential cases of spinal manifestations of systemic disease, although using a routine spine protocol may simplify workflow (Table 1). Given the necessity for total neuraxis imaging in many of these patients, acquisition of volumetric pulse sequences (thus allowing high-fidelity multiplanar reconstructions) versus acquiring equal field-of-view cervicothoracic and thoracolumbar sagittal sequences may reduce

Background

Spinal neuroarthropathy uncommonly occurs in patients with loss of sensation, proprioception, and abnormal range of motion, resulting in destruction of the joint capsule and ligaments.1, 2 Repeated stress produces microfractures, callus formation, joint dislocation, and bone destruction.

Presentation

Patients present late in the disease process with spinal instability. A high index of suspicion is required to make a diagnosis early in the disease process, because pain is typically much less severe than

Summary

Numerous systemic diseases may manifest with spinal involvement, which makes approaching these cases a challenge for the interpreting radiologist. By compartmentalizing the imaging findings into musculoskeletal versus nervous system processes, digging into the electronic medical record, and carefully examining extraspinal imaging findings (including those found in nonspine imaging examinations), a succinct, appropriate differential diagnosis usually can be synthesized, if a single correct

First page preview

First page preview
Click to open first page preview

References (60)

  • M. Doherty

    New insights into the epidemiology of gout

    Rheumatology

    (2009)
  • E.Y. Chang et al.

    Frequency of atlantoaxial calcium pyrophosphate dihydrate deposition at CT

    Radiology

    (2013)
  • A. Shawky et al.

    Longus colli tendinitis - a review of literature and case series

    SICOT J

    (2017)
  • F.M. de Mello et al.

    Axial gout is frequently associated with the presence of current tophi, although not with spinal symptoms

    Spine (Phila Pa 1976)

    (2014)
  • H. Elgafy et al.

    Spinal gout: a review with case illustration

    World J Orthop

    (2018)
  • C.Y. Chang et al.

    Imaging findings of metabolic bone disease

    Radiographics

    (2016)
  • F. Bandeira et al.

    Bone disease in primary hyperparathyroidism

    Arq Bras Endocrinol Metabol

    (2014)
  • A. Wittenberg

    The Rugger Jersey spine sign

    Radiology

    (2004)
  • B. Arsalanizadeh et al.

    Osteoclastomas (‘brown tumors’) and spinal cord compression: a review

    Clin Kidney J

    (2013)
  • S. Kaneko et al.

    Hemodialysis-related amyloidosis: is it still relevant?

    Semin Dial

    (2018)
  • E. Kiss et al.

    Dialysis-related amyloidosis revisited

    AJR Am J Roentgenol

    (2005)
  • D.J. Theodorou et al.

    Imaging in dialysis spondyloarthropathy

    Semin Dial

    (2002)
  • R. Haupt et al.

    Langerhans cell histiocytosis (LCH): guidelines for diagnosis, clinical work-up, and treatment for patients til the age of 18 years

    Pediatr Blood Cancer

    (2013)
  • Y.H. Liu et al.

    Langerhans’ cell histiocytosis with multisystem involvement in an adult

    Clin Exp Dermatol

    (2007)
  • S. Khung et al.

    Skeletal involvement in Langerhans cell histiocytosis

    Insights Imaging

    (2013)
  • X.S. Peng et al.

    Langerhans’ cell histiocytosis of the spine in children with soft tissue extension and chemotherapy

    Int Orthop

    (2009)
  • A.F. Joaquim et al.

    Radiological evaluation of cervical spine involvement in rheumatoid arthritis

    Neurosurg Focus

    (2015)
  • H.V. Nguyen et al.

    Rheumatoid arthritis of the cervical spine

    Spine J

    (2004)
  • A.G. Jurik

    Imaging the spine in arthritis – a pictorial review

    Insights Imaging

    (2011)
  • E.F. Sheybani et al.

    Imaging of juvenile idiopathic arthritis: a multimodality approach

    Radiographics

    (2013)
  • The authors report no conflicts of interest, financial or otherwise, with regard to this article.

    View full text