Literature DB >> 29460010

Type V osteogenesis imperfecta undergoing surgical correction for scoliosis.

Morgan Jones1, Lee Breakwell2, Ashley Cole2, Paul Arundel2, Nick Bishop2.   

Abstract

PURPOSE: The objective of this article is to report a case of type V osteogenesis imperfecta (OI) undergoing posterior instrumented fusion for scoliosis. Type V OI is a moderately severe dysplasia causing primary defects in endochondral bone ossification or mineralisation. It is characterised by hyperplastic callus (HPC) formation, interosseous membrane calcifications, poor bone quality and spinal deformities including scoliosis. Data on the surgical management of spinal deformities in this patient group are lacking. CASE REPORT: A 16-year-old patient with a confirmed diagnosis of type V OI presented with a progressive scoliosis. The patient underwent a T3-L4 posterior instrumented correction and fusion utilising pedicle screws, pedicle hooks and sub-laminar wiring. At 4 months after surgery, the pedicle hooks pulled out and required partial metalwork removal after CT scanning confirmed bony union and no evidence of HPC formation. The patient was successfully discharged with satisfactory correction, confirmed bony union, no neurologic complication and absence of any hyperplastic callus formation.
CONCLUSION: Type V OI patients requiring surgical intervention for scoliosis correction can safely undergo posterior instrumented fusion using sublaminar wiring and pedicle hook/screw constructs without apparent risk of HPC formation around neural elements. Surgery in this patient group remains challenging due to the associated poor bone quality. LEVEL OF EVIDENCE: V.

Entities:  

Keywords:  Hyperplastic ossification; Osteogenesis imperfecta; Scoliosis; Surgery; Type V

Year:  2018        PMID: 29460010     DOI: 10.1007/s00586-018-5465-8

Source DB:  PubMed          Journal:  Eur Spine J        ISSN: 0940-6719            Impact factor:   3.134


  16 in total

Review 1.  Classification of Osteogenesis Imperfecta revisited.

Authors:  F S Van Dijk; G Pals; R R Van Rijn; P G J Nikkels; J M Cobben
Journal:  Eur J Med Genet       Date:  2009-10-28       Impact factor: 2.708

2.  Scoliosis in osteogenesis imperfecta caused by COL1A1/COL1A2 mutations - genotype-phenotype correlations and effect of bisphosphonate treatment.

Authors:  Atsuko Sato; Jean Ouellet; Takeshi Muneta; Francis H Glorieux; Frank Rauch
Journal:  Bone       Date:  2016-02-27       Impact factor: 4.398

3.  Behavior of scoliosis during growth in children with osteogenesis imperfecta.

Authors:  Alireza K Anissipour; Kim W Hammerberg; Angela Caudill; Theodore Kostiuk; Sergey Tarima; Heather Shi Zhao; Joseph J Krzak; Peter A Smith
Journal:  J Bone Joint Surg Am       Date:  2014-02-05       Impact factor: 5.284

4.  Type V OI primary osteoblasts display increased mineralization despite decreased COL1A1 expression.

Authors:  Adi Reich; Alison S Bae; Aileen M Barnes; Wayne A Cabral; Aleksander Hinek; Jennifer Stimec; Suvimol C Hill; David Chitayat; Joan C Marini
Journal:  J Clin Endocrinol Metab       Date:  2014-11-11       Impact factor: 5.958

5.  Genetic heterogeneity in osteogenesis imperfecta.

Authors:  D O Sillence; A Senn; D M Danks
Journal:  J Med Genet       Date:  1979-04       Impact factor: 6.318

6.  Operative treatment of spine deformity in osteogenesis imperfecta.

Authors:  R L Cristofaro; K J Hoek; C A Bonnett; J C Brown
Journal:  Clin Orthop Relat Res       Date:  1979 Mar-Apr       Impact factor: 4.176

7.  Regulation of the bone-restricted IFITM-like (Bril) gene transcription by Sp and Gli family members and CpG methylation.

Authors:  Bahar Kasaai; Marie-Hélène Gaumond; Pierre Moffatt
Journal:  J Biol Chem       Date:  2013-03-24       Impact factor: 5.157

8.  Osteogenesis imperfecta type V: marked phenotypic variability despite the presence of the IFITM5 c.-14C>T mutation in all patients.

Authors:  Frank Rauch; Pierre Moffatt; Moira Cheung; Peter Roughley; Liljana Lalic; Allan M Lund; Norman Ramirez; Somayyeh Fahiminiya; Jacek Majewski; Francis H Glorieux
Journal:  J Med Genet       Date:  2013-01       Impact factor: 6.318

9.  The sagittal balance of the spine in children and adolescents with osteogenesis imperfecta.

Authors:  Karimane Abelin; Raphaël Vialle; Thibault Lenoir; Camille Thévenin-Lemoine; Jean-Paul Damsin; Véronique Forin
Journal:  Eur Spine J       Date:  2008-09-27       Impact factor: 3.134

10.  The spine and surgical treatment in osteogenesis imperfecta.

Authors:  D R Benson; D C Newman
Journal:  Clin Orthop Relat Res       Date:  1981-09       Impact factor: 4.176

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  1 in total

1.  Expert's comment concerning Grand Rounds case entitled "Type V osteogenesis imperfecta undergoing surgical correction for scoliosis" by M. Jones et al. (Eur Spine J; 2018: doi 10.1007/s00586-018-5465-8).

Authors:  C Birkenmaier
Journal:  Eur Spine J       Date:  2018-01-31       Impact factor: 3.134

  1 in total

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