Research Article Volume 2 Issue 6
1Depatment of Anatomy, Desh Bhagat Dental College & Hospital, India
2Department of Anatomy, JCD Dental College & Hospital, India
3Department of Pharmacy & Technology, Khalsa College of Pharmacy, India
Correspondence: Ajit Pal Singh, Department of Anatomy, Desh Bhagat Dental College & Hospital, India, Tel 918437053030
Received: July 13, 2016 | Published: August 5, 2016
Citation: Singh A, Sekhon J, Abhilash, et al. Congenital fusion of typical cervical vertebrae. MOJ Anat Physiol. 2016;2(6):166–168. DOI: 10.15406/mojap.2016.02.00066
Developmental anomalies of the vertebral column are common especially in the cervical region and thus become the point of keen interest for a long time to the anatomists and related health professionals. Normal typical cervical vertebrae; i.e., 3rd to 6th are characterized by the presence of small body, triangular spinal canal, foramina transversarium, superior articular facet directed backwards and upward, inferior articular facet directed forward and downwards and a short bifid spine. Abnormalities in any of the features may be associated with neurological signs and symptoms. During routine osteology classes, we found two abnormally fused typical cervical vertebrae specimens in the Department of Anatomy, Desh Bhagat Dental College and Hospital, Sri Muktsar Sahib, Punjab, India. Both pairs of cervical vertebrae were unilaterally fused at the zygapophyseal joints on the right sides and in one of the case the laminas were also fused partially on the right side. Congenitally fused vertebrae results in biochemical stress in the adjoining segments of the vertebral column leading to premature degenerative change and this can lead to consequences like distal tear, spondylosis, among other problems.
Keywords: cervical vertebrae, zygapophyseal joint, congenital anomalies
There are seven cervical vertebrae numbered 1-7 from above downwards that form the basis of the bony skeleton of neck. They are small in size in comparison to thoracic and lumbar vertebrae as they have to carry less weight; and embryologically, the vertebrae develop from somites derived from paraxial mesoderm and differentiate into the sclerotome (ventro-medial part) and dermomiotome (dorso-latrearal part). The sclerotome takes part in the development of the vertebral column. The mesenchymal cells from sclerotome condense to form the centrum (forms the vertebral body), vertebral arches (forms the pedicles, lamine, spine, articular process and transverse process).1 Congenital anomalies are common in the vertebral column.2 Variations in the cervical vertebrae have been recorded for many years in morphological and clinico-radiological studies. Normal typical cervical vertebrae; i.e., 3rd to 6th are characterized by the presence of small body, triangular spinal canal, long and narrow lamina, foramen transversarium, superior articular facet directed backwards and upwards, inferior articular facet directed forwards and downwards and short bifid spine.3 Abnormalities in any of the features may be associated with neurological signs and symptoms of clinical importance. Yin et al.4 analyzed 87 cases with fused cervical vertebrae at C2-C3 and C3-C4 without any malformation, but Erdil et al.5 reported neck pain, muscular weakness of both upper limbs and minor (but intermittent) head and neck pain. The present study was designed to highlight the osteological variation and its clinical correlation for preventing serious complication, misdiagnosis and early treatment.
During the routine osteology classes for BDS 1st year students in the Department of Anatomy at Desh Bhagat Dental College and Hospital, Sri Muktsar Sahib, Punjab, India - we came across two pairs of abnormally fused typical cervical vertebrae. The fused vertebrae were studied along with the normal typical vertebrae and were analyzed and photographed from different aspects.
Figure 1 shows the features of normal typical cervical vertebra. Based on observations, details of the abnormally fused typical cervical vertebrae were as follows:
Congenitally fused cervical vertebrae is one of the primary malformations associated with chorda dorsalis6‒8 that is believed to be due to defects taking place during the development of the occipital and cervical somites.9‒11 It is caused because of the combination of environmental and genetic factors which occur during the 3rd week of pregnancy.12 Its diagnosis is complex in young age because it may give the appearance of a normal disc area, as the ossification of the vertebral body is not complete till adolescence and the cartilage is also not ossified.13 It is important to differentiate between a pathologic condition from it being congenitally-fused cervical vertebrae or acquired.14,15 The later can be associated with conditions like tuberculosis, juvenile rheumatoid arthritis and trauma16 and even with Klippel-Fiel Syndrome.17 In the congenitally-fused vertebrae, the antero-posterior diameter of the vertebra is decreased and the individual measurement of the two vertebrae bodies’ height is equal to the two fused vertebrae height, including the inter-vertebral disc.
Though the fusion may appear silent, but in advanced age it causes degenerative changes in non-segmented cervical regions and also leads to development of hypermobility and degenerative arthritis above and below the fused cervical region, webbed neck, kyphosis, torticollis, compression of nerve roots resulting in hypothesia and paralysis of the concerned parts of the body. Early diagnosis can help in the prevention of degenerative process by motivating the patients to change their lifestyle. For instance, they can avoid undue trauma, extension and rotational maneuvers which may place the spinal cord and vertebral artery at risk.18 In both specimens examined, the vertebrae were fused on the right side at the zygapophyseal joint on the right side and in specimen II the groove for spinal nerve was reduced in size, so it may lead to compression of nerve roots-resulting into hypothesia and paralysis of the concerned parts of the body. Thus, diagnosis of congenital fusion of C2-C3 is helpful in treating and managing the related complicated outcomes yet to be appeared and its knowledge can further assist in planning the surgeries of head and neck.
None.
Author declares that there is no conflict of interest.
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