Literature DB >> 8855465

Incidence of scoliosis in beta-thalassemia and follow-up evaluation.

P Korovessis1, D Papanastasiou, M Tiniakou, N G Beratis.   

Abstract

STUDY
DESIGN: One hundred fifteen of 120 patients with beta-thalassemia followed in the thalassemia unit were studied for the presence of scoliosis. Forty-nine of these patients were reevaluated 1 year later.
OBJECTIVES: To determine the frequency and the course of scoliosis in beta-thalassemia and to compare the findings with those of patients with idiopathic scoliosis. SUMMARY AND BACKGROUND DATA: There is only one report indicating increased frequency of scoliosis in a limited number of patients with thalassemia. In this study, the authors assessed the frequency of scoliosis in a large sample of patients and followed the evolution of this spinal deformity.
METHODS: Patients with beta-thalassemia aged 3-35 years were examined clinically and radiologically for scoliosis. Forty-nine of them were reexamined 1 year later for determination of the evolution of scoliosis.
RESULTS: Lateral curves of at least 5 degrees Cobb were found in 77 patients (67%), with a male-to-female ratio of 0.9. Scoliosis of at least 10 degrees was found in 21.7% of the male and 20% of the female patients with thalassemia. The ratio was 1.18 for curves of at least 10 degrees and 0.77 for curves of a smaller magnitude. The most common curve pattern was the left lumbar (35.1%), followed by the double-curve pattern (16.9%). Forty-nine randomly selected patients (42.6%) of the 115 included in the study were reexamined 1 year later. Seven male and 7 female patients (total, 28.6%) showed a progression of at least 5 degrees. Six patients (12.2%) experienced spontaneous improvement of less than 6 degrees. The pattern and the evolution of scoliosis observed in patients with beta-thalassemia differ from those found in Greek children with idiopathic scoliosis.
CONCLUSIONS: The findings of this study show that the incidence, evolution, and etiology of scoliosis in beta-thalassemia differ from those of idiopathic scoliosis, indicating that the spinal deformities in patients with beta-thalassemia represents a distinct type of scoliosis. Longer follow-up is needed to investigate the natural history of this type of scoliosis.

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Year:  1996        PMID: 8855465     DOI: 10.1097/00007632-199608010-00015

Source DB:  PubMed          Journal:  Spine (Phila Pa 1976)        ISSN: 0362-2436            Impact factor:   3.468


  5 in total

Review 1.  Endocrine complications of thalassemia.

Authors:  D Tiosano; Z Hochberg
Journal:  J Endocrinol Invest       Date:  2001-10       Impact factor: 4.256

2.  [Arthropathy in beta-thalassemia minor].

Authors:  J Richter; C Specker; U Mödder; M Schneider
Journal:  Med Klin (Munich)       Date:  2000-01-15

Review 3.  Dual-energy X-ray absorptiometry pitfalls in Thalassemia Major.

Authors:  Fabio Pellegrino; Maria Chiara Zatelli; Marta Bondanelli; Aldo Carnevale; Corrado Cittanti; Monica Fortini; Maria Rita Gamberini; Melchiore Giganti; Maria Rosaria Ambrosio
Journal:  Endocrine       Date:  2019-07-12       Impact factor: 3.633

Review 4.  Assessment and treatment of pain in thalassemia.

Authors:  Ashutosh Lal
Journal:  Ann N Y Acad Sci       Date:  2016-04-28       Impact factor: 5.691

5.  Physiopathology of Bone Modifications in β-Thalassemia.

Authors:  Carlo Perisano; Emanuele Marzetti; Maria Silvia Spinelli; Cinzia Anna Maria Callà; Calogero Graci; Giulio Maccauro
Journal:  Anemia       Date:  2012-05-30
  5 in total

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