基于督脉理论辨治脊髓疾病——中医脑病理论与临床实证研究（八）

脊髓充贯椎骨管腔、传导脑髓神机、调控躯体神机、脊髓濡养全身躯体及脏腑、脑脊液循环代谢自有常度。督脉循行脊髓,反映脊髓的大部分功能,督脉为通真之路,脊髓为脏真聚所。例举颈脊髓外伤后遗症神经源性膀胱并神经源性直肠、T₁₂-L₁水平椎管内多发性肿瘤术后、脊髓空洞症3个医案,阐释了脊髓病变以脏腑经络病变为基础,具有易虚损、易痹阻、易共病的病机特征。脊髓疾病属于督脉病变的一部分,治疗上以恢复督脉阴阳水火升降之通道为原则,要同时兼顾督脉病和髓病的用药特点。治督脉应与相关经脉同治,形神同治;虚者治肾命为主,实者通经络为要,治神者参考脑病;治髓虚实主于肝胆,尚用风药。脊髓疾病用药不拘定法,必须辨病辨证,分别轻重缓急处理。     

Application of ventriculoperitoneal shunt as a treatment for hydrocephalus in a dog with syringomyelia and Chiari I malformation

A twenty-month-old Chihuahua male dog was presented to us suffering with ataxia. Based on the physical examination, X-ray and magnetic resonance imaging (MRI) examinations, we diagnosed the dog with hydrocephalus, Chiari I malformation and syringomyelia. Treatment consisted of internal medical treatment and the placement of a ventriculoperitoneal (VP) shunt. The ventricular dilatation was relieved and the dog improved neurologically; however, the Chiari I malformation and syringomyelia remained after surgically positioning the VP shunt.     

CEREBROSPINAL FLUID SIGNAL-VOID SIGN IN DOGS

The cerebrospinal fluid signal-void sign is an observable signal loss from cerebrospinal fluid (CSF), especially on T2-weighted magnetic resonance (MR) images. In people, this sign is attributed to rapid CSF flow or turbulence from arterial pulsations and occurs more frequently with reduced intracranial compliance. The purposes of this study were to describe the CSF signal-void sign, document whether a similar sign occurs in dogs and investigate associations between it and other conditions. The sample population consisted of 327 dogs admitted for neurocranium evaluation using a 0.2 T system. Review of the medical records and MR images was performed to characterize the presence and location of a CSF signal-void sign, ventricular size, syringomyelia, and other lesions. A CSF signal-void sign was detected in at least the mesencephalic aqueduct in 59/327 (18.0%) dogs, including some with no morphologic brain abnormality. The majority of these dogs (45/59% or 76%) weighed <15 kg. In two other dogs, a CSF signal-void sign was detected only in a cervical syrinx. In dogs weighing >15 kg, a CSF signal-void sign was seen with various conditions. In 137/327 (41.9%) dogs weighing <15 kg, the presence of a CSF signal-void sign in the aqueduct (45 dogs) was associated with syringomyelia ( P =0.0468) and increased ventricular size ( P =0.0054): syringomyelia also was associated with increased ventricular size ( P =0.0009). In conclusion, a CSF signal-void sign was seen in dogs with various conditions. In small-breed dogs, a CSF signal-void sign in the aqueduct was associated with ventricular enlargement and syringomyelia.     

Cerebrospinal fluid flow on time‐spatial labeling inversion pulse images before and after treatment of congenital hydrocephalus in a dog

A 3‐month‐old male cross‐breed dog presented with signs of progressive diffuse brain disease. Noncommunicating congenital hydrocephalus concurrent with cervical syringomyelia was diagnosed on magnetic resonance images. On time‐spatial labeling inversion pulse (Time‐SLIP) images CSF flow through the mesencephalic aqueduct was poorly defined and there was flow into the syrinx across the craniocervical junction. After percutaneous ventricular drainage and ventriculoperitoneal shunting, CSF flow through the aqueduct was clearly detected and flow into the syrinx disappeared. In addition, CSF flow in the subarachnoid space at the pons and ventral aspect of the cervical subarachnoid space was restored. Signs of neurological dysfunction improved after ventriculoperitoneal shunting and the cerebral parenchyma was increased in thickness on 2‐year follow‐up computed tomography images. Patterns of CSF flow on Time‐SLIP images before and after CSF drainage or ventriculoperitoneal shunting aid in clarifying disease pathogenesis and confirm effects of CSF drainage.     

Spina bifida with associated malformations of the central nervous system in Dorper-cross sheep

Abstract

CASE HISTORY: In 2008, six lambs within a flock of Dorpercross sheep were born with musculoskeletal and neurological disease. Clinical signs included hindlimb weakness, and urinary incontinence.

CLINICAL FINDINGS: All lambs had focal, inverted areas of alopecic skin over the caudal sacrum, and short, often kinked tails. Four affected lambs were subject to euthanasia, and necropsied. On gross examination, the arches of sacral vertebrae were absent, and spinal nerves and meninges were adherent to the overlying subcutis. Other gross lesions included narrow, elongated skulls, herniation of the occipital lobes into the caudal fossas, hydrocephalus, and syringomyelia. One lamb had coning of the cerebellar vermis, but cerebellar herniation through the foramen magnum was not identified.

DIAGNOSIS: Spina bifida, with associated malformations of the central nervous system.

CLINICAL RELEVANCE: Examination of breeding records suggested either an autosomal recessive or partially penetrant autosomal dominant pattern of inheritance. Because of the associated tail lesions it is proposed that the pathogenesis of this syndrome involves a defect in development of the tail bud (secondary neurulation), that tethering of the spinal cord resulted in the clinical signs, and abnormal pressure of the cerebral spinal fluid resulted in the defects in the skull and brain.     

Chiari 1/syringomyelia complex in a King Charles Spaniel

A 9-year-old King Charles Spaniel presented with a history of progressive forelimb weakness and paroxysmal involuntary flank scratching over a 2-year period. Neurological examination suggested a myelopathy of C1 to C4 spinal cord segments. Advanced imaging studies revealed hydrocephalus, caudal herniation of part of the caudal lobe of the cerebellum through the foramen magnum and marked syrinx formation to the level of the caudal thoracic spine, resembling Arnold-Chiari malformation with secondary hydromyelia in humans. Mechanical obstruction at the craniocervical junction, altering CSF flow dynamics, may lead to syrinx formation. Response to diuretic therapy was moderate but surgical decompression may offer better long term prognosis.     

Signs consistent with syringobulbia may be detected in dogs undergoing MRI

Syringobulbia is a pathologic condition characterized by one or more fluid‐filled cavities within the brainstem. This retrospective case series describes observations in eight dogs with syringobulbia diagnosed during MRI. All dogs were adult, small‐breed dogs with concurrent syringomyelia and neurologic deficits localized to sites rostral to the spinal cord, which cannot be explained by syringomyelia (eg, six dogs had vestibular signs). On MRI, the fluid‐filled cavities had signal intensity characteristics like cerebrospinal fluid, were in the medulla oblongata, and were solitary in each dog. Initially, the shape of the cavity was a slit in five dogs and bulbous in two dogs. Magnetic resonance imaging was repeated in five dogs (6‐55 months of age). One dog had progression of syringobulbia from slit‐like to bulbous, and four dogs had unchanged slit‐like syringobulbia. One dog developed slit‐like syringobulbia after cranioplasty. A variety of medical and surgical treatments were performed with improvement of some but not all clinical signs. One dog died following surgery due to cardiopulmonary failure and the other seven dogs were alive at least 1 year after the initial diagnosis, which was the least time of follow‐up. One surviving dog developed a unilateral hypoglossal nerve deficit 2 months after the initial diagnosis and megaesophagus 14 months later. In conclusion, detecting a fluid‐filled cavity in the medulla oblongata consistent with syringobulbia is possible in dogs undergoing MRI. The cavity is likely acquired, slit‐like or bulbous, progressive, or static, and might be associated with breed size and neurologic signs localized to the medulla oblongata.     

OCCIPITAL DYSPLASIA AND ASSOCIATED CRANIAL SPINAL CORD ABNORMALITIES IN TWO DOGS

Occipital dysplasia was found in association with cervical spinal cord abnormalities in two dogs. One dog presented for tetraparesis and cervical hyperesthesia, the other for historical cervical hyperesthesia and mild paraparesis. In dog 1, a midline cervical spinal cord defect consistent with a communicating syrinx was found. In the other dog, a presumptive syringo/hydromyelia of the cervical spinal cord was found on magnetic resonance imaging. While occipital dysplasia alone is not thought to cause any clinical abnormalities, the dogs of this report suggest that intramedullary central nervous system abnormalities may be present concurrently with occipital dysplasia and should be considered as a possible cause of the clinical signs. The relationship between occipital dysplasia and syringo/hydromyelia in these dogs remains unclear, however, similar associated abnormalities are occasionally found in humans with Chiari malformation.