Page 681 - Withrow and MacEwen's Small Animal Clinical Oncology, 6th Edition
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CHAPTER 31  Tumors of the Nervous System  659



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            D                                                   E                       F











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                           • Fig. 31.1  MRI and pathologic phenotypes of canine brain tumors causing multifocal intracranial clinical
                           signs. (A) MRI of a cerebral meningioma with marked perilesional edema and transtentorial (arrow) and
                           foramen magnum herniations (arrowhead). (B) MRI (left) and gross specimen (right) of primitive neuroec-
                           todermal tumor causing mass effect in both cerebral hemispheres and obliterating the lateral and third
                           ventricles. (C) MRI of multiple meningiomas. A dural tail sign (arrow) can be seen associated with parasel-
                           lar mass. (D) MRI (left) and gross specimen (right) of multifocal metastatic hemangiosarcoma. (E) MRI of
                           butterfly glioblastoma demonstrating bilaterally symmetric wing-like tumor extensions into both cerebral
                           hemispheres. (F) MRI of a choroid plexus carcinoma resulting in obstructive hydrocephalus, fourth ven-
                           tricular dilatation, and syringohydromyelia.

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           hydrocephalus, and intracranial hemorrhage.  In early stages of   of tumor involving the frontal lobe, falcine or subtentorial
           tumor growth, compensatory autoregulatory mechanisms, such   brain herniations, and marked contrast enhancement of the
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           as decreased cerebrospinal fluid (CSF) production and shifting   tumor.  In cats, the overall incidence of tumor-associated epi-
           of CSF into the spinal subarachnoid space, are effective at main-  lepsy is lower than dogs, with approximately 25% of cats with
           taining  the  intracranial  pressure  within  physiologic  ranges.  For   brain tumors experiencing seizures. 3,24,29  In one study, seizures
           some slow-growing tumor types, such as meningiomas, intracra-  were more common in cats with glioma (27%) and lymphoma
           nial pressure–volume homeostatic regulatory mechanisms can   (26%) than meningioma (15%).  Behavioral changes are the
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           remain surprisingly intact despite large tumor volumes associated   most frequently reported clinical sign associated with feline brain
           with significant mass effect; however, with progressive increases in   tumors, being observed in 16% to 67% of cats. 3,29  Central ves-
           tumor volume, autoregulatory mechanisms become overwhelmed   tibular dysfunction is the most common clinical manifestation
           and  intracranial  hypertension  (ICH)  develops.  ICH,  and  the   of brain tumors affecting the brainstem. 26,30  Nonspecific com-
           resulting detrimental decrease in cerebral perfusion pressure, is   plaints (e.g., lethargy, inappetance) were identified in more than
           the common pathophysiologic denominator underlying many of   20% of cats with brain tumors and are frequently reported in
           the primary and secondary mechanisms of tumor-associated brain   dogs with pituitary tumors. 3,31
           injury. Acute clinical deterioration observed in animals with brain   Tumors involving forebrain structures are more common than
           tumors and ICH is often the result of vasogenic or interstitial (i.e.,   those in the brainstem. 1–3,30  In many cases with solitary masses,
           obstructive hydrocephalus) brain edema, abnormalities of cerebral   observed neurologic deficits are reflective of the focal neuroana-
           blood flow (ischemia or hemorrhage), brain herniations, or com-  tomic area involved. However, dogs and cats may present with
           binations of these mechanisms (Figs. 31.1A, B). 25    neurologic deficits indicative of multifocal intracranial disease
             A  brain  tumor  should  be  considered  as  a  differential  diag-  (see Fig. 31.1).
           nosis in any middle-aged or older animal with a clinical history   In 50% of dogs with solitary PBTs, multifocal signs result from
           consistent with peracute, acute, or chronic brain dysfunction,   the tumor or its secondary effects involving multiple region of
           especially if clinical signs are progressive. In dogs, seizures are   the brains.  The phenotype of some PBTs, such as butterfly glio-
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           the most common clinical manifestation of intracranial neo-  blastomas, by definition requires tumor invasion of both cerebral
           plasia and occur in approximately 50% of dogs with forebrain   hemispheres.  Multiple tumors may also be present, which occurs
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           tumors. 2,26–28  The index of suspicion for a brain tumor should   occasionally in canine meningiomas, but is seen in approximately
           increase in dogs that experience a new onset of seizure activity   20% of cats with meningiomas. 3,33,34  Canine oligodendrogliomas
           after 5 years of age, especially in at-risk breeds.  Significant risk   can manifest with multifocal or diffuse leptomeningeal involve-
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           factors for tumor-associated structural epilepsy based on mag-  ment.  Rare case reports describing synchronous PBTs of dif-
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           netic resonance imaging (MRI) diagnosis include the presence   ferent histologies and synchronous PBTs and SBTs also exist.
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