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
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