Dens agenesis and cervical vertebral malformation in a Labrador Retriever puppy
Authors Salas E, Cerny HE, Harris S
Received 20 June 2014
Accepted for publication 9 September 2014
Published 18 December 2014 Volume 2015:6 Pages 11—15
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Editor who approved publication: Professor Takashi Agui
Elisa N Salas,1 Henry E Cerny,2 Seth P Harris1
1Institute of Agriculture and Natural Resources, School of Veterinary Medicine and Biomedical Sciences, University of Nebraska–Lincoln, Lincoln, NE, USA; 2Yankee Hill Veterinary Hospital, Lincoln, NE, USA
Abstract: Cervical vertebral malformations can cause acute or progressive pain, paralysis, and potentially death. Herein we present a case report of dens agenesis; cervical vertebral malformations of C1, C2, C6, and C7; subluxation of C1 and C2 and C4 and C5; and associated degenerative myelopathy in a 5-month-old female Labrador Retriever puppy. We additionally review current knowledge regarding pathogenesis and treatment.
Keywords: atlantoaxial subluxation, cervical vertebral malformation, dog, dens agenesis, myelopathy
A 5-month-old silver female Labrador Retriever was presented for nightly episodes of whining and restlessness, which the owners attributed to pain. The puppy was otherwise healthy with no prior medical conditions.
Clinical and gross findings
Physical examination revealed a bright, alert, and responsive patient with pain on palpation of the dorsal cervical and thoracic region of the spinal column. Maxillary brachygnathism and mandibular malposition of incisors 301 and 401 were noted. Complete blood count was unremarkable. Radiographs of the spinal column were performed under sedation. Radiographs revealed osseous malformations confined to the cervical spinal column. These findings included subluxation of the atlantoaxial articulation and shortening of the dorsal spinous process of the axis (Figure 1A and B), subluxation of C4–C5 articulation, and lack of rectangular shape of C6 and C7 vertebral bodies (Figure 1A). Conservative analgesic therapy was elected and the patient was discharged with oral carprofen at 2 mg/kg and tramadol hydrochloride at 2.5 mg/kg every 12 hours. Twenty-eight days later, due to increasing unmitigated pain, the owners elected euthanasia and postmortem evaluation.
Necropsy confirmed the maxillary and mandibular findings. The cervical spinal cord and visceral organs were fixed in formalin. The spinal column and skull were boiled and cleaned to better visualize the skeletal malformations. Skull abnormalities found were incomplete fusion of the ventral aspect of the foramen magnum and a small keyhole defect within the occipital bone. Atlas malformations included bilaterally misshapen cranial articular processes, elongation of these processes into the ventral arch, bilaterally symmetric transverse folds of the cranial articular foveae, an approximately 4 mm long fissure of the caudal vertebral arch, and flattening of the caudal articular processes (Figure 2A and B). On the caudal tubercle of the atlas, there was a caudal flattened semicircular, 15 mm diameter callus, which apposed a 12 mm long spade-shaped callus on the cranial aspect of the spinous process of the axis (Figures 2A and 3B). Other changes in the axis included lack of the dens and bilateral flattening of the cranial articular processes (Figure 3A). All cervical and thoracic vertebral bodies examined had incomplete fusion of the ventral aspect of the vertebral foramina. Gaps of approximately 3–4 mm diameter with a depth <1 mm ran the length of the vertebrae.
Histologic evaluation was performed on sections of caudal brainstem, spinal cord segments from the atlas and atlantoaxial junction, and the visceral organs. Sections bordering the caudal brainstem and at the junction of C1 and the foramen magnum had few dilated axon sheathes and few spheroids; these lesions were randomly scattered. The section from the junction of C1 and C2 contained several spheroids and dilated axon sheaths (Figure 4). The white matter contained a few medium-sized, poorly circumscribed areas of rarefaction and infiltration by microglia. The associated blood vessels were lined by hypertrophied endothelial cells and contained frequent marginating monocytes. Many spheroids were associated with this area of gliosis. Additionally, in the section from C1 to C2, the vacuoles were most prominent bilaterally within the dorsal and dorsolateral funiculi. The sections from the viscera did not have clinically significant lesions.
Figure 4 Photomicrograph of the spinal cord taken at C1. Scattered small to medium spheroids and axonal swelling are indicators of axonal degeneration (arrow). Artifactual spongiosis is present. Hematoxylin and eosin stain; bar =50 μm.
- Dens agenesis with atlantoaxial subluxation and multiple cervical and thoracic vertebral osseous defects
- Degenerative myelopathy, multifocal, chronic, mild.
The primary lesion in this case was the agenesis of the dens, resulting in instability of the atlantoaxial articulation. This caused the clinical signs of pain due to spinal cord compression. Agenesis of the dens has classically been attributed to trauma with secondary ischemia and necrosis, or due to congenital lack of the ossification center.1 In this case we suspect that this lesion developed due to a congenital lack of the ossification center caused by a primary ventral midline fusion defect. This suspicion is based on the young age of the dog and the presence of other midline fusion defects (eg, occipital bone malformation and the incomplete fusion of the vertebral bodies within the ventral aspect of the vertebral canals).
Although a common condition, pathogenesis of dens agenesis is unknown in both humans and animals. First described in 1933, it was termed os odontoideum syndrome.2 As in dogs, hypothesized parthenogeneses include either lack for formation of traumatization.3 In humans, ossification of the dens begins by 3 years of age and is complete late in life, leaving this process vulnerable to injury.3 In the dog, dens formation begins much earlier at approximately 30 days of age in utero, and ossification in the dog is complete as early as 6 weeks of age.4,5 Thus, our patient’s defect is believed to be congenital rather than traumatic. In dogs, not all dens agenesis cases progress, as evidenced by a Rottweiler aged 9.5 years who first presented with signs at 6 months of age and lacked worsening and was euthanized due to a recurrent oral sarcoma.6 Familial mode of inheritance is recognized in the Arabian horse (Watson), but, to date, no genetic marker has been identified.7 With sequencing of the dog genome, analysis of genetics of affected patients may hold promise of finding a genetic basis of this disease.
During the initial clinical evaluation, a number of possible differential diagnoses were considered, including Chiari-like malformation, occipitoatlantoaxial malformation, and atlantoaxial instability or subluxation. Chiari-like malformation is a congenital lesion consisting of supraoccipital hypoplasia, which causes a decreased diameter of the foramen magnum.8 When secondary lesions are present, they can include cerebellar herniation, compression of the medulla, and destruction of the dorsal subarachnoid space. Secondary impairment in cerebrospinal fluid can occur, with resulting syringomyelia or hydromyelia.9 Cavalier King Charles Spaniels and Griffon Bruxellois dogs are overrepresented.10 Cavalier King Charles Spaniels have a suspected autosomal recessive gene defect with incomplete penetrance.8
Occipitoatlantoaxial malformation typically arises due to bilateral fusion of the atlas to the occipital bones of the skull with dens hypoplasia.1 This can cause secondary changes such as narrowing of the foramen magnum with compression of the brainstem or cervical spinal cord. Detection of this lesion can be made with palpation, imaging studies, or necropsy.
Atlantoaxial instability, or subluxation, is an umbrella term that includes nonunion of the dens with axis, aplasia or hypoplasia of the dens, or lack of the transverse ligament of the axis.2,11 It is more commonly reported in toy breed dogs, with Miniature and Toy Poodles, Chihuahuas, Pekingese, Pomeranian, and Yorkshire Terrier dogs being predisposed.12,13 There are a few reports of this condition in large breed dogs, cats, lambs, horses, and a camel.6,7,14–16 Clinical signs include cervical pain and guarding, upper motor neuron deficits of all four limbs with progression to tetraperesis, or, rarely, paralysis of all four limbs with worsening of signs upon flexion of the neck. Primary lesions of the dens, such as aplasia and hypoplasia, occur more frequently than absence of the transverse ligament.17 Also reported are morphologic abnormalities of C1 and C2. Clinical signs can be attributed to spinal cord compression with resultant syringomyelia, axonopathy, neuronal necrosis, and edema. Radiography can reveal signs of subluxation but may not identify the primary lesion.18 Myelography can confirm a subluxation as well and possibly show syringomyelia. However, magnetic resonance imaging can be diagnostic antemortem and has the added benefit of avoiding postprocedural seizures seen in affected patients with myelography.
The patient also had deviation of the C4–C5 junction or malformation of C6 and C7 vertebral bodies, which did not manifest clinically or during physical examination. This was confirmed by gross examination of the body. Histology was not pursued of the caudal spinal cord. Cervical vertebral malformations have been reported in Doberman Pinschers, Basset Hounds, and Bernese Mountain Dogs.19–22 Pathogenesis is associated with congenital or prenatal conditions in the Doberman Pinscher. However, genetic markers have yet to be defined (Rusbridge et al). Findings can include loss of rectangularity of vertebral bodies, stenosis of the foramina of the bodies, intervertebral disc disease, joint capsule proliferation, spinous process cranial deviation and enlargement, articular process osteoarthritis, and hypertrophy of the ligamentum most frequently at the C4–C5 junction. A literature search of caudal cervical vertebral malformation failed to reveal concurrent atlantoaxial malformations. Thus, definitive pathogenesis of these two conditions is unknown. However, we speculate that a heritable defect is likely with a nondominant pathogenesis due to lack of affected siblings. Although histological evaluation of the spinal cord alone would not have revealed a specific etiology, the skeletal malformations observed indicated that compressive forces from skeletal malformations caused the degenerative changes. Microscopic examination also served to eliminate other causes of spinal cord disease, such as primary inflammatory, degenerative, or neoplastic conditions.
The goal of treatment of atlantoaxial instability is stabilization and resolution of spinal cord compression.12,23,24 Conservative management is indicated for patients with mild clinical signs, acute signs, or dogs who have incomplete physeal ossification.23 Therapy includes immobilization of the head and neck positioned in extension with a cervical splint (ventrally reinforced), corticosteroids, and exercise restriction for a period of 6 weeks with a reported 50%–63% success rate.23 Multiple surgical techniques have been performed and include dorsal atlantoaxial stabilization, left hemilaminectomy, ventral stabilization, transarticular fixation with pins, lag screw fixation, and a modified ventral fixation.12,13,24 Surgical fixation can halt progression or allow for reversal of clinical signs. The most common complications include hardware migration, failure of fixation with subluxation, and intraoperative brain stem trauma.
Treatment of cervical vertebral malformations is reserved for patients with clinical signs associated with myelopathy. Such myelopathy can cause spinal cord compressive lesions or intervertebral disc instability with subsequent extrusion of disc material. These conditions are corrected with ventral slot decompression.19
Antemortem, the patient displayed pain but lacked neurologic deficits. As pain management therapy had failed to provide satisfactory amelioration of the clinical signs, and calluses had developed on the articular facets of the atlas and axis due to chronic instability, it is questionable whether conservative management would have been successful long term. As spinal cord compression resulted only in pain rather than neurologic deficits, the patient may have been amenable to surgical stabilization.
No outside financial support was provided.
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