Chapter 19. Nervous System Neoplasia
Joan R. Coates and Gayle C. Johnson
PRIMARY BRAIN TUMORS
Incidence
Brain tumors develop with a frequency of 14.5 in 100,000 dogs 1 and 2.2 to 3.5 in 100,000 cats. 1,2 The tumor classification system most widely used is from the World Health Organization Classification System and can be found in Table 19-1 . Meningioma is the most common brain tumor in dogs and cats 3-5 and accounts for approximately 45% of primary intracranial neoplasms in dogs 4,5 and 59% in cats. 3 Glial cell tumors are the second most common primary brain tumor in dogs 3,5 and the fourth most common in cats. 3 Brain tumors typically affect older dogs with a median age of 9 years (range, 4–13 years) and 95% are older than 5 years of age. 4 Golden Retrievers and Boxer dogs are at increased risk for intracranial neoplasia. 5 Dolichocephalic breeds may be at increased risk for meningiomas, whereas brachycephalic breeds may have increased risk for gliomas. 5 Cats with brain tumors are older with a mean age of 11.3 ± 3.8 years (range, 0.5–21.5 years). 3 Male cats are affected slightly more than female cats (male:female ratio of 1.5:1). 3 The domestic shorthair cat is the most common breed identified. 3
Tissue/Region | Cell Origin | Subtype |
---|---|---|
Tumors of neuroepithelial tissue | Astrocytic tumors | Fibrillary Protoplasmic Gemistocytic Anaplastic Glioblastoma |
Oligodendroglial tumors | Oligodendroglioma Anaplastic | |
Other gliomas | Mixed glioma Gliosarcoma Gliomatosis cerebri Spongioblastoma | |
Ependymal tumors | Ependymoma Anaplastic | |
Choroid plexus tumors | Choroid plexus papilloma Choroid plexus carcinoma | |
Neuronal tumors | Gangliocytoma Ganglioglioma Neuroblastoma Ganglioneuroma Paraganglioma | |
Embryonal tumors | Primitive neuroectodermal tumors Neuroblastoma Ependymoblastoma Epithelioneuroblastoma | |
Pineal parenchymal tumors | Pineocytoma Pineoblastoma | |
Meningeal tumors | Meningioma | Meningotheliomatous Fibrous Transitional Psammomatous Angiomatous Papillary Granular cell Myxoid Anaplastic |
Mesenchymal tumors | Fibrosarcoma Diffuse meningeal sarcomatosis | |
Hematopoietic tumors | Lymphoma | Primary Secondary |
Neoplastic reticulosis | ||
Microgliomatosis | ||
Malignant histiocytosis | ||
Tumors of sellar region | Suprasellar germ cell tumor | |
Pituitary tumors | Pituitary adenoma Pituitary carcinoma | |
Craniopharyngioma | ||
Other primary tumors/cysts | Hamartoma | |
Cysts | Epidermoid Pituitary Other | |
Tumors of peripheral nervous tissue | Peripheral nerve sheath tumor | Schwannoma Neurofibroma Malignant schwannoma Neurofibrosarcoma |
Metastatic tumors | Local extension | |
Hematogenous |
Etiology and Risk Factors
Definitive risk factors for development of brain tumors are unknown for dogs and cats. Inheritance may have a role in some breeds of dogs. Hormones such as estrogen and progesterone can influence tumor genesis. 7,8 Young cats with mucopolysaccharidosis type I have a high incidence of meningiomas, providing suspicion for a genetic basis. 9
Clinical Features
Clinical signs of brain tumors develop as a result of damage to surrounding normal neural tissue from tumor expansion and associated edema. 10 Brain edema is a prominent feature of intracranial neoplasms. Brain edema may initially cause few or no clinical signs. As the edema worsens, a mass effect occurs with distortion and displacement of brain tissue, subsequently causing a rise in intracranial pressure 11 and shift of brain tissue to areas of lower pressure. Neurologic deficits produced by these displacements are additive to the clinical signs caused by the tumor itself. 12 Table 19-2 summarizes clinical signs associated with herniation. Hydrocephalus may also occur, either as a result of altered cerebrospinal fluid (CSF) resorption or ventricular obstruction. 13,14
Herniation Type | Anatomic Displacement | Clinical Signs |
---|---|---|
Foramen magnum | Caudal displacement of cerebellum and compression of medulla and cerebellum | Tetraplegia (flaccid) Pupils midposition to dilated Loss of brainstem reflexes Apnea Coma Opisthotonus |
Caudal transtentorial | Herniation of temporal cortex and compression of midbrain and traction of oculomotor nerve | Pupils dilated (asymmetric) Loss of brainstem reflexes Tetraplegia Apnea Coma Opisthotonus |
Rostral transtentorial | Compression of rostral cerebellum against the tentorium | Possible cerebellar dysfunction Decerebellate posture |
Cingulate gyrus (falcine) | Movement of the cingulated gyrus beneath the falx and compression of opposite cingulated gyrus | Possible forebrain dysfunction Circling Head pressing Seizures Abnormal mentation |
Diagnosis and Staging
Common neurologic signs observed in animals with brain tumors include altered mentation (obtundation, stupor, coma), seizures, ataxia, circling, and behavioral changes. Seizures (45%) are the most common clinical sign in dogs, but circling (23%), ataxia (21%), and head tilt (13%) also occur. 15 Brain neoplasia should be considered as a differential diagnosis when a dog has its first seizure after 4 years of age. 4 Clinical signs in cats are similar but often are vague or nonspecific, with anorexia and lethargy being most common. Reported neurologic signs in cats include altered mentation (26%), circling (23%), seizures (23%), ataxia (16.9%), and behavioral changes (15.6%). 3 A sudden onset of aggression is the most common behavioral change reported in cats. 3
A minimum database including a complete blood count, serum biochemical analysis, and urinalysis should be performed to evaluate for metabolic abnormalities in animals suspected of having a brain tumor. Radiographs of the thorax and abdomen as well as abdominal ultrasound are recommended to rule out metastatic and concurrent disease prior to advanced diagnostics and surgery. 5 Neuroanatomic localization of the central nervous system (CNS) lesion will vary based on location of the tumor and amount of mass effect caused by the edema and tumor. 16,17 Table 19-3 summarizes clinical signs associated with specific lesion localization within the brain.
Intracranial Division | Brain Region | Clinical Signs |
---|---|---|
Supratentorial (rostral to the osseous tentorium) | Cerebral cortex | Seizures Obtundation/stupor or normal mentation Behavioral abnormalities Ipsilateral circling with normal gait Contralateral menace response deficit Contralateral loss of touch and pain recognition Contralateral postural reaction deficits Cervical spinal pain |
Diencephalon | Obtundation/stupor Normal gait (compulsive) or circling Cranial nerve (CN) II deficits Loss of thermoregulation Abnormal eating or drinking Endocrine dysfunction Cervical spinal pain | |
Infratentorial (caudal to the osseous tentorium) | Brainstem | Obtundation/stupor Vestibular dysfunction (central) < div class='tao-gold-member'>
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