Page 691 - Withrow and MacEwen's Small Animal Clinical Oncology, 6th Edition
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CHAPTER 31  Tumors of the Nervous System  669


           study, the posttreatment neurologic status was the only signifi-  tumors are euthanized at or near the time of diagnosis because of
           cant prognostic factor where a nonambulatory status was sig-  poor prognosis or failure to respond to palliative therapy. 134,135  
                                         129
                                            Two dogs with CSAs
           nificantly associated with shorter STs.
  VetBooks.ir  treated with surgery alone both had a recurrence of clinical signs   Tumors of Cranial, Paraspinal, and Peripheral
           because of imaging confirmed tumor recurrence within 5 months
           of surgery. 130                                       Nerves
             Cats with malignant vertebral tumors also have a guarded to
           poor long-term prognosis with surgical treatment, with a reported   Classification, Epidemiology, and Comparative
           MST of 3.7 months in one study. 133  The literature indicates that   Pathology
           common contemporary veterinary neurosurgical techniques are
           generally insufficient to attain the goal of en bloc surgical excision   Peripheral nerve tumors (often collectively called  peripheral
           of vertebral tumors, which is critical to the therapeutic outcome   nerve sheath tumors [PNSTs]) are uncommon in dogs and rare in
           in humans. 129,130,133  Thus, although currently largely unexplored   cats. PNSTs may arise from Schwann cells, perineurial cells, or
           in veterinary medicine, aggressive surgical techniques, including   intraneural fibroblasts. Descriptive terminology that reflects the
           vertebrectomy with vertebral stabilization, will likely become an   cellular origin of these tumors (schwannoma, neurofibroma, neu-
           important component of advancing the surgical treatment of ver-  rofibrosarcoma) is not routinely used because of the inherent level
           tebral and SC tumors. 153                             of difficulty in determining the tissue of origin of these tumors
             Currently, there is insufficient information to clearly identify   in veterinary medicine. Instead, PNSTs are divided into benign
           the superior method of treatment of solitary vertebral plasma cell   peripheral nerve sheath tumors (BPNSTs) or malignant peripheral
           tumors in dogs and cats. Solitary plasmacytomas have been treated   nerve sheath tumors (MPNSTs) based on microscopic evidence of
           successfully with surgery, RT, and various combinations of these   malignancy. 157–159  This latter classification scheme is more use-
           modalities. 132,154                                   ful from a clinical standpoint, as the majority of reported PNSTs
             Dogs with nephroblastomas treated with surgery and RT may   in dogs are histologically and biologically aggressive tumors. Cats
           also experience improved functional outcomes and STs compared   have a higher proportion of BPNSTs compared with dogs. 158
           with those not treated surgically, although reported MSTs vary   PNSTs may arise in any cranial nerve, spinal nerve root, or
           widely. 142,143  In one study, MST for dogs that were not treated   somatic or autonomic peripheral nerve. 157–160  PNSTs occur most
           surgically was 1 day compared with 71 days for dogs that under-  commonly  in middle-aged  to older  dogs of medium  and large
           went cytoreductive surgery. 142  Another investigation reported that   breeds. No breed or sex predilection has been noted. The most
           dogs with nephroblastoma treated with cytoreductive surgery or   frequently affected cranial nerve is the trigeminal nerve, and the
           RT survived longer (MST 374 days) than dogs treated palliatively   most common spinal nerve roots affected are in the caudal cervical
           (MST 55 days). 143  Tumors confined to an ID-EM location were   region (C6–T2) followed by nerves of the lumbar intumescence
           associated with superior STs (MST 380 days) than tumors with   (Fig. 31.7). 157–160  Metastasis is rare. Secondary tumors, such as
           IM involvement (MST 140 days). 143  As nephroblastoma affects   lymphoma, malignant sarcomas, HS, and hamartomas, can occa-
           young dogs, the literature suggests that the majority of dogs will   sionally involve peripheral nerves. 136,138,139  In cats, diffuse infiltra-
           experience life-limiting local tumor recurrence or treatment com-  tive peripheral nerve lymphoma (neurolymphomatosis) is usually
           plications regardless of treatment type. 142,143      B-cell origin, but one case of peripheral T-cell lymphoma in an
             The outcomes associated with other specific types of SC tumors   FeLV-positive cat has been reported. 161,162  In dogs, peripheral
           are unknown owing to very limited numbers of reported cases that   nerve lymphoma is typically of T-cell origin. 136  
           received treatment, and in some instances, cases received RT treat-
           ment without histologic confirmation of the type of lesion being   Pathophysiology, History, and Clinical Signs
           treated. 155  A few case reports suggest that primary IM neuroep-
           ithelial neoplasms may be resected if well-demarcated and that   As with brain and spinal tumors, the clinical signs of PNSTs reflect
           long-term successful outcomes are possible with combinations of   the location of the tumor. As the majority of reported canine
           surgery, with and without RT. 156  However, most animals with IM   PNSTs involve the nerve roots and/or nerves of the brachial and















            A                         B                          C                        D

                           • Fig. 31.7  MRI and pathologic features of PNST. (A) Postcontrast MRI of C7 MPNST manifesting as thick-
                           ening and contrast enhancement of the affected nerve, as well as intradural invasion. (B) At necropsy, a
                           MPNST appears as nodular masses on the C7, C8, and T1 nerves. Bar = 1.5 cm. (C) Dorsal MRI image of
                           a sciatic PNST causing enlargement of hyperintensity of the affected nerve (arrow). (D) MRI of a trigeminal
                           PNST with compression of the midbrain and atrophy of the muscles of mastication ipsilateral to the tumor.
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