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2.6




            Noninfectious inflammatory disorders


















            Although a number of noninfectious inflammatory    contrast enhancement characteristics as described
              disorders  of the brain of the dog  and cat have been   for CT (Figures 2.6.1, 2.6.2). 1,3,5
            reported, two entities, granulomatous meningoencepha-  Meningeal involvement is documented in many
            litis and necrotizing encephalitis, are the most common   patients with GME, and abnormal imaging findings are
            and best described.  Necrotizing encephalitis can be   sometimes limited to prominent meningeal enhance-
                              1
              further subdivided into necrotizing meningoencephali-  ment (Figure 2.6.1). In a minority of patients, imaging
            tis and necrotizing leukoencephalitis, and it is possible   may be normal or lesions may not contrast enhance. 1,5
            that these represent different manifestations of the same
            disease. All three of these conditions are thought to be   Necrotizing encephalitis
            autoimmune disorders.
                                                               Necrotizing meningoencephalitis

            Granulomatous meningoencephalitis                  Necrotizing meningoencephalitis, sometimes referred to
                                                               as Pug dog encephalitis, is a nonsuppurative, necrotiz-
            Granulomatous meningoencephalitis (GME) is an      ing, inflammatory brain disorder.  Small‐ and toy‐breed
                                                                                           8
              idiopathic inflammatory disorder of the central nervous   dogs are predisposed, and Pug, Maltese, and Chihuahua
            system, characterized by perivascular mononuclear cell   breeds are highly overrepresented. Median age of onset
            infiltrates.  Young to middle‐aged (4–5 years), female,   is 1.5–3 years, and females are affected more commonly
                     2
            small‐ and toy‐breed dogs are predisposed, while the   than males. Lesions may be focal or asymmetrically
            disorder is less common in large‐breed dogs and rare   multifocal and involve both gray and white matter of
            in cats. Lesion distribution may be focal, disseminated   the  cerebral hemispheres and overlying meninges. 1,8–10
            (multifocal), or ocular, with the focal and disseminated   Cerebellar and brainstem involvement, though uncom-
            forms predominating. Lesions primarily involve white   mon, has been reported.  Grossly, lesions are frequently
                                                                                   11
            matter,  but  gray  matter  and  meninges  may  also  be   cavitary and associated with significant brain swelling
            affected. This disorder most often affects the forebrain,   from inflammation and edema. 8
            brainstem, or spinal cord, with the cerebellum and optic   Lesions may be hypoattenuating on unenhanced
            nerves less frequently involved. 1–7               CT images when cavitary or when associated with sig-
               Depending on the extent of associated edema,    nificant brain edema. Edema may also induce midline
            lesions may have ill‐defined hypoattenuation on    shift, brain herniation, and other features of mass effect.
            unenhanced CT images and will variably contrast    Contrast enhancement is variable on CT, ranging from
            enhance. Enhancement can be absent, heterogeneous   absent  to moderate,  but when present, the enhance-
            and ill-defined, or may sometimes reveal a well‐   ment pattern is heterogeneous and margins may be
            delineated mass. Lesions are typically T1 iso‐ to   poorly delineated. On MR images, lesions are T1 iso‐ or
            hypointense and T2 hyperintense and have similar   hypointense and T2 hyperintense, involve the cerebral


            Atlas of Small Animal CT and MRI, First Edition. Erik R. Wisner and Allison L. Zwingenberger.
            © 2015 John Wiley & Sons, Inc. Published 2015 by John Wiley & Sons, Inc.
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