Congenital costo-vertebral fibrous band and congenital kyphoscoliosis: a previously unreported combination

被引：1
|
作者：
Eid, Tony [1 ]
Ghostine, Bachir [1 ]
Kreichaty, Gaby [1 ]
Daher, Paul [2 ]
Ghanem, Ismat [1 ]
机构：
[1] Hotel Dieu France Hosp, Dept Orthoped Surg, Beirut, Lebanon
[2] Hotel Dieu France Hosp, Dept Pediat Surg, Beirut, Lebanon
来源：
EUROPEAN SPINE JOURNAL | 2013年 / 22卷
关键词：
Congenital; Kyphoscoliosis; Fibrous; Bands; MUSCULAR TORTICOLLIS; SCOLIOSIS; KYPHOSIS; GENES;
D O I：
10.1007/s00586-012-2570-y
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
Congenital kyphoscoliosis (CKS) results from abnormal vertebral chondrification. Congenital fibrous bands occur in several locations with variable impact on vertebral development. We report a previously unreported case of a female infant with CKS presenting with an L2 hypoplastic vertebra and a costo-vertebral fibrous band extending to the skin in the form of a dimple. We also describe the therapeutic approach, consisting of surgical excision of the fibrous band and postoperative fulltime bracing, with a 7-year follow-up. We recommend a high index of suspicion in any unusual presentation of CKS and insist on case by case management in such cases.
引用
收藏
页码：S424 / S428
页数：5
相关论文
共 50 条
  • [31] Short-term X-ray Results of Posterior Vertebral Column Resection in Severe Congenital Kyphosis, Scoliosis, and Kyphoscoliosis
    Ozturk, Cagatay
    Alanay, Ahmet
    Ganiyusufoglu, Kursat
    Karadereler, Selhan
    Ulusoy, Levent
    Hamzaoglu, Azmi
    SPINE, 2012, 37 (12) : 1054 - 1057
  • [32] Comparison of pedicle subtraction osteotomy and vertebral column resection in adolescent congenital kyphoscoliosis and the influencing factors on intraoperative hemorrhage: a retrospective study
    Shi, Baina
    Pan, Xiaofeng
    Lu, Weiguang
    Zheng, Nengfang
    Zhu, Guangcai
    Yang, Jun
    AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH, 2025, 17 (01): : 622 - 633
  • [33] Anterior and Posterior Vertebral Column Resection Versus Posterior-only Technique A Comparison of Clinical Outcomes and Complications in Congenital Kyphoscoliosis
    Demirkiran, Gokhan
    Dede, Ozgur
    Karadeniz, Emre
    Olgun, Deniz
    Ayvaz, Mehmet
    Yazici, Muharrem
    CLINICAL SPINE SURGERY, 2017, 30 (07): : 285 - 290
  • [34] A de novo variant in AMOTL1 gene in an adult with craniofacial abnormalities and previously unreported congenital diaphragmatic hernia
    Lee, Paul
    Gooch, Catherine
    GENETICS IN MEDICINE, 2022, 24 (03) : S102 - S102
  • [35] A Rare Co-occurrence of Lumbo-Costo-Vertebral Syndrome With Congenital Lumbar Hernia in a Six-Year-Old Child
    Dhabalia, Rishabh
    Kashikar, Shivali, V
    Parihar, Pratapsingh
    Mishra, Komal
    Yadav, Riya
    Bothara, Shivani S.
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (07)
  • [36] A single posterior approach for multilevel modified vertebral column resection in adults with severe rigid congenital kyphoscoliosis: a retrospective study of 13 cases
    Yan Wang
    Yonggang Zhang
    Xuesong Zhang
    Peng Huang
    Songhua Xiao
    Zheng Wang
    Zhengsheng Liu
    Baowei Liu
    Ning Lu
    Keya Mao
    European Spine Journal, 2008, 17 : 361 - 372
  • [37] A single posterior approach for multilevel modified vertebral column resection in adults with severe rigid congenital kyphoscoliosis: a retrospective study of 13 cases
    Wang, Yan
    Zhang, Yonggang
    Zhang, Xuesong
    Huang, Peng
    Xiao, Songhua
    Wang, Zheng
    Liu, Zhengsheng
    Liu, Baowei
    Lu, Ning
    Mao, Keya
    EUROPEAN SPINE JOURNAL, 2008, 17 (03) : 361 - 372
  • [38] Congenital Kyphoscoliosis in Monozygotic Twins: Ten-Year Follow-up Treated by Posterior Vertebral Column Resection (PVCR) A Case Report
    Chang, Dong-Gune
    Yang, Jae Hyuk
    Lee, Jung-Hee
    Kim, Young-Hoon
    Kim, Jin-Hyok
    Suh, Seung-Woo
    Ha, Kee-Yong
    Suk, Se-Il
    MEDICINE, 2016, 95 (17)
  • [39] Identification of previously unreported mutations in CHRNA1, CHRNE and RAPSN genes in three unrelated Italian patients with congenital myasthenic syndromes
    Brugnoni, Raffaella
    Maggi, Lorenzo
    Canioni, Eleonora
    Moroni, Isabella
    Pantaleoni, Chiara
    D'Arrigo, Stefano
    Riva, Daria
    Cornelio, Ferdinando
    Bernasconi, Pia
    Mantegazza, Renato
    JOURNAL OF NEUROLOGY, 2010, 257 (07) : 1119 - 1123
  • [40] Identification of previously unreported mutations in CHRNA1, CHRNE and RAPSN genes in three unrelated Italian patients with congenital myasthenic syndromes
    Raffaella Brugnoni
    Lorenzo Maggi
    Eleonora Canioni
    Isabella Moroni
    Chiara Pantaleoni
    Stefano D’Arrigo
    Daria Riva
    Ferdinando Cornelio
    Pia Bernasconi
    Renato Mantegazza
    Journal of Neurology, 2010, 257 : 1119 - 1123
12345