Nervous System Neoplasia

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
TABLE 19-1 HISTOLOGIC CLASSIFICATION OF TUMORS OF THE NERVOUS SYSTEM (Adapted and modified from Koestner A, Bilzer T, Fatzer R, et al: Histological classification of tumors of the nervous system of domestic animals [WHO international classification of tumors of domestic animals], Washington DC, 1999, Armed Forces Institute of Pathology.)
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
TABLE 19-2 CLINICAL SIGNS OF BRAIN HERNIATION SYNDROME
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
TABLE 19-3 CLINICAL SIGNS ASSOCIATED WITH INTRACRANIAL LOCALIZATIONS
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
Get Clinical Tree app for offline access