Scheuermann Disease

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Scheuermann Disease

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Scheuermann, or Scheuermann’s, disease (juvenile kyphosis) is a deformity in the thoracic or thoracolumbar spine in which pediatric patients have an increased kyphosis along with backache and localized changes in the vertebral bodies. [1, 2] See the image below.

Scheuermann’s disease refers to osteochondrosis of the secondary ossification centers of the vertebral bodies. The lower dorsal and upper lumbar vertebrae are involved initially. The process may be limited to several bodies or may involve the entire dorsal and lumbar spine.

Scheuermann’s disease probably is heterogeneous (ie, not a single entity but a group of conditions sharing similar features).

Lateral radiography of the spine demonstrates diagnostic changes in Scheuermann’s disease. [3, 4] Sorenson suggested the following radiologic criteria for the diagnosis of the condition:

The treatment of Scheuermann’s disease is controversial. [5, 6] Some authors think that the natural history of thoracic Scheuermann’s disease is benign and that therefore the condition needs no treatment. Whether orthotics or surgical treatments prevent any of the consequences that may occur is uncertain.

When the kyphosis is relatively severe, recommendations include casting, a spinal brace, or rest and recumbency on a rigid bed. Orthotic management of Scheuermann’s disease usually requires 12-24 months of treatment.

Surgery rarely is indicated in patients with Scheuermann’s disease. Probably the two most common indications for surgery are spinal pain and unacceptable cosmetic appearance. These criteria are subjective, so it is wise to be cautious in counseling these patients. [7]

In patients with curves greater than 75° and with pain that is unresponsive to nonoperative measures, consider spinal fusion. Spinal fusion consists of an anterior release and fusion, as well as a posterior instrumentation and fusion performed under the same anesthesia on the same day.

Cord decompression is indicated for the rare patients who have neurologic deficits secondary to epidural cysts or increased kyphotic angulation.

Scheuermann’s disease refers to osteochondrosis of the secondary ossification centers of the vertebral bodies. The lower dorsal and upper lumbar vertebrae are involved initially. The process may be limited to several bodies or may involve the entire dorsal and lumbar spine.

Scheuermann’s disease probably is heterogeneous (ie, not a single entity but a group of conditions sharing similar features). The etiology and pathogenesis are a matter of debate. Many theories have been advanced, including mechanical, metabolic, and endocrinologic causes.

A definite hereditary component is involved in the development of the condition, but the mode of inheritance has been debated. [8] Reports of identical radiologic changes in monozygotic twins and transmission over 3 generations suggested underlying heritability. In study by McKenzie and Sillence, 12 probands were referred, and upon radiologic examination of their parents and siblings, 7 were shown to have familial Scheuermann’s disease with an autosomal dominant pattern of inheritance. [9] Of the remaining 5 probands, 4 had chromosomal anomalies.

Patients with Scheuermann’s disease generally are affected at age 13-16 years, are taller [10] than comparably aged peers, and have advanced skeletal versus chronologic age. Some affected children have disproportionate limb lengths.

A Greek research report, however, found that although, in the study, children with Scheuermann’s disease tended to be taller and weigh more than did other children, there seemed to be no correlation in children with the disease between these 2 factors and the magnitude and morphology of the main kyphotic curve. [10] The authors suggested that hormonal disturbances may be impacting the development of Scheuermann’s disease and also causing, as a secondary result, height and weight increases.

A study by Hershkovich et al, however, suggested that height and body mass index (BMI) are associated with the risk and severity of spinal deformities in adolescents. The study, which involved the medical records of 829,791 males and females aged 17 years, including 103,249 who had been diagnosed with some degree of kyphosis or scoliosis, found a significantly higher rate of spinal deformities, and a greater likelihood of such deformities being severe, in underweight males and females. Greater height was also found to be associated with increased risk and greater severity of spinal deformities in males and females. [11]

In a Finnish study, left-handedness was found to be a powerful determinant of hyperkyphosis in school children before puberty. [12] An increased incidence of spondylolysis and spondylolisthesis also was reported in patients with Scheuermann’s disease, and scoliosis in the region of kyphosis is reported in 20-30% of patients as well. [13]

According to some authors, the presence of an adjacent area of lordoscoliosis below the region of hyperkyphosis testifies to the common nature of the pathogenesis of idiopathic scoliosis and Scheuermann’s disease. Scheuermann’s disease may be associated with an epidural cyst with an ensuing neurologic deficit.

A retrospective study by Tyrakowski et al found no significant difference between skeletally mature and skeletally immature patients with Scheuermann’s disease with regard to radiographic sagittal spinopelvic parameters, including sagittal vertical axis, thoracic kyphosis, thoracolumbar kyphosis, lumbar lordosis, pelvic incidence, pelvic tilt, and sacral slope. However, both groups (33 patients each) had a significantly lower pelvic incidence and sacral slope than did children, adolescents, and adults without Scheuermann’s disease, causing the investigators to question the use of pelvic incidence in predicting the desired lumbar lordosis in Scheuermann’s disease cases. [14]

A study by Peleg et al suggested that a greater horizontal orientation of the sacrum may lead to a change in spinal biomechanics that in turn contributes significantly to the development of Scheuermann’s disease. The study involved the evaluation of the sacral anatomical orientation in 183 persons with Scheuermann’s disease and 185 controls. [15]

United States

The prevalence rate of Scheuermann’s disease is thought to be 0.4-8%.

International

A study by Armbrecht et al using found the prevalence of Scheuermann’s disease in Europe to be 8% in persons aged 50 years and above, with no difference between males and females. The sample, consisting of more than 10,000 individuals, came from 27 centers across Europe that participated in the European Vertebral Osteoporosis Study. [16]

Many authors believe that there are few adverse long-term sequelae of Scheuermann’s disease, despite a paucity of available natural history data. Lowe suggests that if residual kyphosis remains less than 60º at skeletal maturity, the patient has an excellent prognosis for minimal problems in adult life.

Pain may be present but generally ceases when growth is complete. Minimal spinal malalignment may persist when the disorder becomes quiescent. Early development of marginal osteophytes may occur. Acute myelopathy secondary to cord compression at the apex of the thoracic kyphosis has been reported.

Using the exercise tolerance test, a prospective, comparative study by Lorente et al found that adolescent Scheuermann’s disease patients with kyphosis of over 75° displayed significant respiratory inefficiency, with ventilation capacity and maximum oxygen uptake being lower than in healthy controls. [17]

A study by Liu et al suggested that a link exists between Scheuermann’s disease and thoracolumbar disk herniation (disk herniation between T10/11 and L1/2). The investigators found that the radiographic signs of Scheuermann’s disease, as well as the diagnosis of Scheuermann’s disease itself, were significantly more prevalent in the 63 patients in the study with symptomatic thoracolumbar disk herniation than they were in a group of 57 patients who underwent surgery for lower lumbar disk herniation. Moreover, in the patients with thoracolumbar disk herniation, the herniation was significantly more prevalent at segments displaying the radiographic signs of Scheuermann’s disease than at segments that did not. [18]

 

Scheuermann’s disease affects boys more frequently than it does girls.

Scheuermann’s disease affects children aged 13-16 years, and the diagnosis is rarely made in patients younger than 10 years.

Bettany-Saltikov J, Turnbull D, Ng SY, Webb R. Management of Spinal Deformities and Evidence of Treatment Effectiveness. Open Orthop J. 2017. 11:1521-47. [Medline]. [Full Text].

Mansfield JT, Bennett M. Scheuermann Disease. 2018 Jan. [Medline]. [Full Text].

Summers BN, Singh JP, Manns RA. The radiological reporting of lumbar Scheuermann’s disease: an unnecessary source of confusion amongst clinicians and patients. Br J Radiol. 2008 May. 81(965):383-5. [Medline].

Bhatia NN, Chow G, Timon SJ, Watts HG. Diagnostic modalities for the evaluation of pediatric back pain: a prospective study. J Pediatr Orthop. 2008 Mar. 28(2):230-3. [Medline].

de Mauroy J, Weiss H, Aulisa A, Aulisa L, Brox J, Durmala J, et al. 7th SOSORT consensus paper: conservative treatment of idiopathic & Scheuermann’s kyphosis. Scoliosis. 2010 May 30. 5:9. [Medline]. [Full Text].

Tsirikos AI, Jain AK. Scheuermann’s kyphosis; current controversies. J Bone Joint Surg Br. 2011 Jul. 93(7):857-64. [Medline].

Vetrile ST, Kuleshov AA, Shvets VV, et al. [Operative treatment of severe spine deformities]. Vestn Ross Akad Med Nauk. 2008. 34-40. [Medline].

Damborg F, Engell V, Nielsen J, et al. Genetic epidemiology of Scheuermann’s disease. Acta Orthop. 2011 Oct. 82(5):602-5. [Medline].

McKenzie L, Sillence D. Familial Scheuermann disease: a genetic and linkage study. J Med Genet. 1992 Jan. 29(1):41-5. [Medline].

Fotiadis E, Kenanidis E, Samoladas E, Christodoulou A, Akritopoulos P, Akritopoulou K. Scheuermann’s disease: focus on weight and height role. Eur Spine J. 2008 May. 17(5):673-8. [Medline].

Hershkovich O, Friedlander A, Gordon B, et al. Association between body mass index, body height, and the prevalence of spinal deformities. Spine J. 2013 Oct 19. [Medline].

Nissinen M, Heliovaara M, Seitsamo J, et al. Left handedness and risk of thoracic hyperkyphosis in prepubertal schoolchildren. Int J Epidemiol. 1995 Dec. 24(6):1178-81. [Medline].

Segatto E, Lippold C, Vegh A. Craniofacial features of children with spinal deformities. BMC Musculoskelet Disord. 2008 Dec 22. 9:169. [Medline]. [Full Text].

Tyrakowski M, Janusz P, Mardjetko S, et al. Comparison of radiographic sagittal spinopelvic alignment between skeletally immature and skeletally mature individuals with Scheuermann’s disease. Eur Spine J. 2014 Oct 4. [Medline].

Peleg S, Dar G, Steinberg N, Masharawi Y, Hershkovitz I. Sacral orientation and Scheuermann’s kyphosis. Springerplus. 2016. 5:141. [Medline]. [Full Text].

Armbrecht G, Felsenberg D, Ganswindt M, et al. Vertebral Scheuermann’s disease in Europe: prevalence, geographic variation and radiological correlates in men and women aged 50 and over. Osteoporos Int. 2015 Oct. 26 (10):2509-19. [Medline].

Lorente A, Barrios C, Lorente R, Tamariz R, Burgos J. Severe hyperkyphosis reduces the aerobic capacity and maximal exercise tolerance in patients with Scheuermann disease. Spine J. 2018 Jul 17. [Medline].

Liu N, Chen Z, Qi Q, et al. The relationship of symptomatic thoracolumbar disc herniation and Scheuermann’s disease. Eur Spine J. 2014 May. 23(5):1059-66. [Medline].

Haveman LM, van Es HW, ten Berge-Kuipers M. [Complaints of back pain in childhood: find curable causes]. Ned Tijdschr Geneeskd. 2008 Feb 16. 152(7):353-8. [Medline].

Riddle EC, Bowen JR, Shah SA, et al. The duPont kyphosis brace for the treatment of adolescent Scheuermann kyphosis. J South Orthop Assoc. 2003. 12(3):135-40. [Medline].

Riouallon G, Morin C, Charles YP, et al. Posterior-only versus combined anterior/posterior fusion in Scheuermann disease: a large retrospective study. Eur Spine J. 2018 Sep. 27 (9):2322-30. [Medline].

Polly DW Jr, Ledonio CG, Diamond B, et al. What are the Indications for Spinal Fusion Surgery in Scheuermann Kyphosis?. J Pediatr Orthop. 2017 Jan 30. [Medline].

Soo CL, Noble PC, Esses SI. Scheuermann kyphosis: long-term follow-up. Spine J. 2002 Jan-Feb. 2(1):49-56. [Medline].

Nasto LA, Perez-Romera AB, Shalabi ST, Quraishi NA, Mehdian H. Correlation between preoperative spinopelvic alignment and risk of proximal junctional kyphosis after posterior-only surgical correction of Scheuermann kyphosis. Spine J. 2016 Apr. 16 (4 Suppl):S26-33. [Medline].

Jozef E Nowak, MD Consulting/Admitting Physiatrist, Division of Physical Medicine and Rehabilitation, Kelowna General Hospital

Jozef E Nowak, MD is a member of the following medical societies: American Academy of Physical Medicine and Rehabilitation, Canadian Medical Association, College of Physicians and Surgeons of British Columbia, Royal College of Physicians and Surgeons of Canada

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Received salary from Medscape for employment. for: Medscape.

Michael T Andary, MD, MS Professor, Residency Program Director, Department of Physical Medicine and Rehabilitation, Michigan State University College of Osteopathic Medicine

Michael T Andary, MD, MS is a member of the following medical societies: American Academy of Physical Medicine and Rehabilitation, American Association of Neuromuscular and Electrodiagnostic Medicine, American Medical Association, Association of Academic Physiatrists

Disclosure: Serve(d) as a speaker or a member of a speakers bureau for: Allergan<br/>Received honoraria from Allergan for speaking and teaching. for: Allergan.

Stephen Kishner, MD, MHA Professor of Clinical Medicine, Physical Medicine and Rehabilitation Residency Program Director, Louisiana State University School of Medicine in New Orleans

Stephen Kishner, MD, MHA is a member of the following medical societies: American Academy of Physical Medicine and Rehabilitation, American Association of Neuromuscular and Electrodiagnostic Medicine

Disclosure: Nothing to disclose.

Elizabeth A Moberg-Wolff, MD Medical Director, Pediatric Rehabilitation Medicine Associates

Elizabeth A Moberg-Wolff, MD is a member of the following medical societies: American Academy for Cerebral Palsy and Developmental Medicine, American Academy of Physical Medicine and Rehabilitation

Disclosure: Nothing to disclose.

Scheuermann Disease

Research & References of Scheuermann Disease|A&C Accounting And Tax Services
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Scheuermann Disease

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