Literature DB >> 19308574

New classification and score for tibial hemimelia.

Michael Weber1.   

Abstract

PURPOSE: Previous classifications of tibial malformations are no longer sufficient and practical for clinics and treatment. They are not precisely defined, include incorrect pathological-anatomical definitions, are related to X-ray diagnosis only, miss complete formal types of malformation, or describe too complex concepts not useful for clinical applications (Jones et al., J Bone Joint Surg B 60:31-39, 1978; Kalamchi and Dawe, J Bone Joint Surg B 67:581-584, 1985; Henkel et al., Arch Orthop Trauma Surg 93:1-19, 1978). More precise preoperative diagnosis, including by sonography and MRI and experienced intraoperative analysis of anatomical structures ensure exact description of the pathological-anatomical situation which can be used because of new potential in therapy. Until now, no score was available for detection of additional limb malformations and, therefore, clinical and scientific comparison of the different tibial reduction deficiencies, especially in respect to the success of therapy, was not sufficiently realisable. A new classification and score is presented reflecting the improved therapy currently available.
METHODS: In this classification and score the main pathological findings of the complete leg are included (coxa-femur-patella-tibia-fibula-pes), with specific importance of the tibia. Tibial malformations are divided into seven main groups and five of them into two subgroups. The cartilaginous anlage of the tibia which has not yet received much attention in the literature plays an important role in this classification. Only seven main types of tibial defect have to be recognized and, if necessary, additional defects of the whole leg, including the function of the affected parts, can be summarized in a-five-class-system.
RESULTS: With this classification and this score system which was evaluated on 95 affected limbs, with a sex ratio of 51%:49% (male:female), right:left affection, and unilateral:bilateral affection also, we found the sequence of the distribution of types as follows: 61% of cases with type-VII, 15% with type-III, 6% with type-I, 6% with type-V, 5% with type-II, 3% with type-IV, and 3% with type-VI. In comparison with the Jones et al. (J Bone Joint Surg B 60:31-39, 1978), Kalamchi and Dawe (J Bone Joint Surg B 67:581-584, 1985) and Henkel et al. (Arch Orthop Trauma Surg 93:1-19, 1978) classifications the tibial defects in the presented classification are detected more precisely, the pathological anatomical terms are correctly used, the whole leg and all main functions are included and, thus, reference to therapeutical possibilities is given.
CONCLUSIONS: The new classification and the score system allow simple, therapeutically relevant, and comprehensive classification and, additionally, scientific comparison of the different pattern of defects described by diverse authors. For daily clinical use the tibial classification only is preferred.

Entities:  

Year:  2008        PMID: 19308574      PMCID: PMC2656800          DOI: 10.1007/s11832-008-0081-5

Source DB:  PubMed          Journal:  J Child Orthop        ISSN: 1863-2521            Impact factor:   1.548


  4 in total

1.  Congenital aplasia and dysplasia of the tibia with intact fibula. Classification and management.

Authors:  D Jones; J Barnes; G C Lloyd-Roberts
Journal:  J Bone Joint Surg Br       Date:  1978-02

2.  [An international terminology for the classification of congenital limb deficiencies. Recommendations of a working group of the international society for prosthetics and orthotics (author's transl)].

Authors:  H L Henkel; H G Willert; C Gressmann
Journal:  Arch Orthop Trauma Surg       Date:  1978-12-12

3.  [Nation-wide registration of limb deficiencies in Germany].

Authors:  M Weber; S Schröder; P Berdel; F U Niethard
Journal:  Z Orthop Ihre Grenzgeb       Date:  2005 Sep-Oct

4.  Congenital deficiency of the tibia.

Authors:  A Kalamchi; R V Dawe
Journal:  J Bone Joint Surg Br       Date:  1985-08
  4 in total
  13 in total

1.  Unclassified tibial hemimelia.

Authors:  Vishnu Senthil; Imthias V Kottamttavide; Hitesh Shah
Journal:  BMJ Case Rep       Date:  2016-06-08

Review 2.  [Congenital tibial hemimelia].

Authors:  S Farr; R Ganger; F Grill
Journal:  Orthopade       Date:  2014-11       Impact factor: 1.087

3.  Tibial hypoplasia with a bifid tibia: an unclassified tibial hemimelia.

Authors:  Krupa Shah; Hitesh Shah
Journal:  BMJ Case Rep       Date:  2016-08-16

Review 4.  Systematic radiographic evaluation of tibial hemimelia with orthopedic implications.

Authors:  Katia Kaplan-List; Nina B Klionsky; James O Sanders; Michael E Katz
Journal:  Pediatr Radiol       Date:  2017-01-03

5.  Tibial hemimelia associated with GLI3 truncation.

Authors:  Steven Deimling; Chris Sotiropoulos; Kimberly Lau; Sonia Chaudhry; Kendra Sturgeon; Simon Kelley; Unni Narayanan; Andrew Howard; Chi-Chung Hui; Sevan Hopyan
Journal:  J Hum Genet       Date:  2016-01-21       Impact factor: 3.172

6.  A case of bilateral tibial hemimelia type VIIa.

Authors:  Selvakumar Chinnakkannan; Rashmi Ranjan Das; K Rughmini; Sufath Ahmed
Journal:  Indian J Hum Genet       Date:  2013-01

Review 7.  Tibial hemimelia: new classification and reconstructive options.

Authors:  Dror Paley
Journal:  J Child Orthop       Date:  2016-12-01       Impact factor: 1.548

8.  Rare case of tibial hemimelia, preaxial polydactyly, and club foot.

Authors:  Guinevere Granite; John E Herzenberg; Ronald Wade
Journal:  World J Clin Cases       Date:  2016-12-16       Impact factor: 1.337

Review 9.  Deformity Reconstruction Surgery for Tibial Hemimelia.

Authors:  David Y Chong; Dror Paley
Journal:  Children (Basel)       Date:  2021-05-31

10.  A rare case of tibial hemimelia, surgical technique and clinical results.

Authors:  Marco Basso; Valentina Camurri; Piero Frediani; Silvio Boero
Journal:  Acta Orthop Traumatol Turc       Date:  2017-12-14       Impact factor: 1.511

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