Literature DB >> 17933313

The frequency and clinical significance of congenital defects of the posterior and anterior arch of the atlas.

Mehmet Senoglu1, Sam Safavi-Abbasi, Nicholas Theodore, Nicholas C Bambakidis, Neil R Crawford, Volker K H Sonntag.   

Abstract

OBJECT: In this study the authors investigated the anatomical, clinical, and imaging features as well as incidence of congenital defects of the C-1 arch.
METHODS: The records of 1104 patients who presented with various medical problems during the time between January 2006 and December 2006 were reviewed retrospectively. The craniocervical computed tomography (CT) scans obtained in these patients were evaluated to define the incidence of congenital defects of the posterior arch of C-1. In addition, 166 dried C-1 specimens and 84 fresh human cadaveric cervical spine segments were evaluated for anomalies of the C-1 arch.
RESULTS: Altogether, 40 anomalies (2.95%) were found in 1354 evaluated cases. Of the 1104 patients in whom CT scans were acquired, 37 (3.35%) had congenital defects of the posterior arch of the atlas. The incidence of each anomaly was as follows: Type A, 29 (2.6%); Type B, six (0.54%); and Type E, two (0.18%). There were no Type C or D defects. One patient (0.09%) had an anterior arch cleft. None of the reviewed patients had neurological deficits or required surgical intervention for their anomalies. Three cases of Type A posterior arch anomalies were present in the cadaveric specimens.
CONCLUSIONS: Most congenital anomalies of the atlantal arch are found incidentally in asymptomatic patients. Congenital defects of the posterior arch are more common than defects of the anterior arch.

Entities:  

Mesh:

Year:  2007        PMID: 17933313     DOI: 10.3171/SPI-07/10/399

Source DB:  PubMed          Journal:  J Neurosurg Spine        ISSN: 1547-5646


  24 in total

Review 1.  Bilateral arcuate foramen associated with partial defect of the posterior arch of the atlas in a medieval skeleton: case report and review of the literature. Looking backward to go forward.

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Journal:  Surg Radiol Anat       Date:  2010-12-14       Impact factor: 1.246

2.  What the mind does not know, the eyes do not see: a rare congenital fusion of the odontoid process to the atlantal hemiarch.

Authors:  Mariapan Sureisen; Ramanand Achannan; Kuan Chon Chong; Chung Chek Wong
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3.  Imaging anatomy and variation of vertebral artery and bone structure at craniocervical junction.

Authors:  Shaoyin Duan; Shaomao Lv; Feng Ye; Qingchi Lin
Journal:  Eur Spine J       Date:  2009-03-14       Impact factor: 3.134

4.  Three-dimensional CT study on the anatomy of vertebral artery at atlantoaxial and intracranial segment.

Authors:  Shaoyin Duan; Hongwei He; Shaomao Lv; Liaobin Chen
Journal:  Surg Radiol Anat       Date:  2009-08-26       Impact factor: 1.246

5.  The prevalence of congenital C1 arch anomalies.

Authors:  Gina Hyun; Emad Allam; Paul Sander; Christopher Hasiak; Yihua Zhou
Journal:  Eur Spine J       Date:  2017-08-28       Impact factor: 3.134

6.  High prevalence of cervical deformity and instability requires surveillance in Loeys-Dietz syndrome.

Authors:  Sara K Fuhrhop; Mark J McElroy; Harry C Dietz; Gretchen L MacCarrick; Paul D Sponseller
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7.  Congenital defect of the posterior arch of C1: a case report.

Authors:  Bilal B Butt; Paul Gagnet; Rakesh Patel; Ilyas Aleem
Journal:  J Spine Surg       Date:  2021-06

8.  Congenital anomaly of combined atlas-odontoid process fusion and bipartite atlas.

Authors:  Jea Ryoung Gil; Wan Tae Kim; Min Jeong Seo
Journal:  Jpn J Radiol       Date:  2015-10-26       Impact factor: 2.374

9.  A neurosurgical view of anatomical evaluation of anterior C1-C2 for safer transoral odontoidectomy.

Authors:  Kagan Tun; Erkan Kaptanoglu; Berker Cemil; S Tuna Karahan; Ali Firat Esmer; Alaiddin Elhan
Journal:  Eur Spine J       Date:  2008-03-20       Impact factor: 3.134

10.  C1 fracture in a patient with a congenital cleft in the posterior arch: report on a failed conservative treatment.

Authors:  Robert Hudek; Guido Wanner; Hans-Peter Simmen; Clément M L Werner
Journal:  BMJ Case Rep       Date:  2013-06-13
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