Keywords
thoracolumbar neoplasia - extradural tumours - nerve sheath tumour - spine - canine
Introduction
Intraspinal neoplasms can involve the spinal cord, dura mater, spinal nerves, or paraspinal
tissues, resulting in clinical signs of spinal dysfunction. According to their location
relative to spinal cord and dura mater, they are classified as intramedullary (IM),
intradural-extramedullary (ID-EM), or extradural (ED).[1]
[2] The ED tumours have been described to account for 50% of all spinal cord neoplasms
in dogs, followed by ID-EM reported with an overall distribution of 35%; IM tumours
are least common, comprising the remaining 15%.[2]
Peripheral nerve sheath tumours (PNSTs) are a heterogeneous group of soft tissue neoplasms,
both benign and malignant, arising from Schwann cells or modified Schwann cells, endoneurial
fibroblasts, or perineural cells.[3] The latest 2007 World Health Organization (WHO) classification of human PNSTs was
adapted to veterinary medicine due to the remarkable gross and histological similarities
of these tumours in people and dogs.[4] According to this classification, there are four major subtypes: schwannoma, neurofibroma,
perineurioma, and malignant peripheral nerve sheath tumour (MPNST).[4] Any part of a nerve or nerve root can be affected, involving spinal nerve roots
in the caudal cervical and cranial thoracic region, nerves contributing to the brachial
plexus,[3]
[5]
[6]
[7] as well as cranial nerves and other peripheral nerves.[3]
[8]
[9]
[10] One report describes schwannoma as being the second most common spinal tumour in
dogs after meningioma.[11] However, compared with other spinal cord affections, such as trauma and intervertebral
disc disease, neoplasms are the least common compressive lesion.[7]
[12]
Current treatment options for spinal tumours include surgical resection,[5]
[6] stereotactic radiation therapy (SRT),[1]
[13]
[14] and, occasionally, chemotherapy.[15] The PNSTs have a high rate of recurrence, and the overall prognosis is considered
poor, depending on the completeness of local resection, spinal cord infiltration and
collateral damage before and during surgery, and on tumour type.[1]
[6]
Herein we report a PNST in a 2-year-old dog, extradurally at T7, which is an infrequent
location,[1]
[3]
[5] and the successful long-term outcome after surgical excision.
Case Description
A 2-year-old, intact female American Staffordshire Terrier, weighing 26 kg, presented
with a 1-month history of hindlimb paraplegia, with no known history of trauma. The
dog underwent previously treatment with prednisone (1 mg/kg q. 12 per os [PO], Prednicortone,
Dechra Veterinary Products S.r.l., Turin, Italy) which temporarily yielded some improvement.
At referral to the reporting institution, the dog presented with non-ambulatory paraparesis,
hypertonic hindlimb muscles, lack of proprioception, and hyperreflexia of the hindlimbs
(patellar and cranial tibial reflex). Deep palpation of the thoracolumbar vertebral
region elicited pain in the T5-T10 area, and the cutaneous trunci reflex was lost
caudal to T10. Complete blood count, serum biochemical examinations, and cardiologic
evaluation were unremarkable.
Magnetic resonance imaging (MRI) and computed tomography scan (CT) were performed
20 days before being referred to the teaching hospital ([Fig. 1]). The CT scan showed a well-defined ED mass (11 × 10 × 18 mm), dorsally to the spinal
cord at the level of T7-T8, causing moderate compression of the dural sac. Contrast-enhanced
CT images confirmed the absence of other alterations affecting the vertebral column.
On MRI, the mass was hyperintense on T1-weighted and short tau inversion recovery
sequences and hypointense on T2-weighted images; mild to moderate heterogeneous contrast
enhancement was present, not extending outside the vertebral canal, with normal profiles
of vertebral bodies and intervertebral foramina. There were no signs attributable
to lung or lymph node metastasis, neither on CT nor on MRI.
Fig. 1 Transverse and sagittal magnetic resonance imaging (MRI) T1-weighted (A, B) and contrast-enhanced computed tomography (CT) (C, D) images of the spina at the level of the caudal end of T7 body. A mass (arrows) is
visible inside the vertebral canal and compressing the underlying spinal cord (asterisk).
The mass appears to be hyperintense in T1-weighted MRIs (A, B) and moderately enhancing in CT images (C, D). L, left; R, right.
The imaging features were most compatible with meningioma, fibrosarcoma, and PNST,
but hemangiosarcoma, lymphosarcoma, plasmacytoma, or inflammatory granuloma could
not be ruled out.[1]
[6]
[16] Surgical exploration, attempting to excise the lesion, was proposed and executed
as follows: after routine premedication and in general anaesthesia, the dog was positioned
in sternal recumbency. Anaesthesia was maintained with isoflurane (Isoflo, Ecuphar
Italia S.r.l., Milan, Italy) in oxygen and fentanyl (Fentadon, Dechra Veterinary Products
S.r.l., Turin, Italy) in constant rate infusion.
A dorsal T7-T8 laminectomy was performed,[17] involving the removal of the spinous process of T7, the dorsal lamina, and caudal
articular processes, while cranial articular processes were preserved ([Fig. 2]). After sufficient exposure of the vertebral canal, a reddish-grey soft tissue mass
was found. The mass had a smooth surface and was loosely attached to the dura mater
with thin connective tissue strands. The spinal cord, as far as visible without durotomy,
had a normal appearance, and no haemorrhages were seen. By gentle blunt dissection,
the mass could be excised entirely, avoiding damage to the dura mater; no unusual
bleeding was encountered, but preventively, a gelatine sponge (GELITA-SPON, Gelita
Medical) was placed on the spinal cord. To manage any residual vertebral instability,
a figure-eight cerclage wire (Ø1.2 mm, Alcyon Italia S.P.A.) was placed between the
spinous processes of T6 and T8. Reconstruction of paraspinal musculature, fascia,
subcutaneous tissues, and the skin was made in routine fashion.
Fig. 2 Intraspinal extradural mass (white arrowhead) at the T7 level during (A) and after removal (B) using a T7-T8 dorsal laminectomy. White X: T6 spinal process.
Postoperative care consisted of carprofen (4 mg/kg q24h SC, Rimadyl, Zoetis Italia
S.r.l., Rome, Italy) and ceftriaxone (25 mg/kg q12h PO, Mylan Italia S.r.l., Milan,
Italy) medication. The patient was ambulatory within 24 hours after surgery and was
discharged after 3 days, exhibiting only mild ataxia.
For histologic examination, the excised tissue was routinely processed for paraffin
sections (4 µm) and stained with haematoxylin and eosin, Masson's trichrome, and Van
Gieson. Histopathological examination revealed a hypercellular, unencapsulated mass,
featuring a population of densely packed spindle-shaped cells, characterized by thin
and eosinophilic cytoplasm, atypical plump, ovoid, single, or multiple nuclei, and
prominent nucleoli ([Fig. 3]). The predominant pattern consisted of areas of interwoven bundles, streams, or
concentric whorls. Moderate cellular pleomorphism and anisokaryosis were observed,
but mitotic figures were infrequent (∼ 0–1 in 10 fields at high power magnification).
Infiltrate characterized by lymphocytes, plasma cells, histiocytoid cells, and rare
macrophages was noted. Van Gieson and Masson's trichrome stain showed scattered stroma
and fine delicate collagen fibres in few areas of the tumour. For further tumour typing,
immunochemistry was performed using a polyclonal antibody against laminin, S-100 protein,
vimentin, and glial fibrillar acid protein (GFAP). Immunohistochemistry revealed that
the neoplasm was immunoreactive for vimentin, GFAP, and S100 protein. Furthermore,
we performed immunohistochemistry using an anti-laminin antibody, and did not observe
immunopositivity for this antibody. Immunoreactivity against those markers was consistent
with a benign PNST.
Fig. 3 Histopathological examination of the resected thoracic mass in ×20 magnification
(A) and ×40 magnification (B). The tumour is composed of a cell population organized in densely packed spindle-shaped
cells. The predominant pattern consisted of areas of interwoven bundles, streams or
concentric whorls. Tumour cells present uniformly intense immunopositivity for vimentin
protein (C), S100 protein (D) and glial fibrillar acid protein (E) (×40).
At 1 week after surgery, there was complete remission of neurological signs, and at
1, 3, 6, and 9 months follow-up, the absence of any neurologic deficits confirmed
full recovery. However, a 13-month follow-up by CT scan ([Figs. 4]–[5]) revealed in the identical localization a small, round-shaped ED lesion within the
vertebral canal, moderately enhancing by contrast medium. No compression on the dural
sac and no further alterations of the spinal cord and vertebral metamere were noted.
These imaging findings were suggestive of scar tissue resulting from surgery, forasmuch
as no neurological signs recurred.
Fig. 4 Transverse computed tomographic images, obtained 13 months after surgery, at the
level of the caudal end of the T7 body, before (A) and after (B) the contrast-medium administration (WW: 360, WL: 60). In the vertebral canal, under
the T7 right caudal articular process (asterisk) a small lesion with slight contrast
enhancement (arrow) is visible. L, left; R, right.
Fig. 5 Right sagittal multiplanar reconstructed images of the thoracic spine (from T5 to
T9), before (A) and after (B) the contrast-medium administration (WW: 360, WL: 60), obtained 13 months after surgery.
In the vertebral canal, under the T7 caudal articular process (asterisk), a small,
rounded lesion with a slight contrast enhancement (arrow) is visible.
At the time of writing, 18 months after surgery, the dog is free of any neurological
and/or clinical signs.
Discussion
The PNSTs are a heterogeneous group of neoplasms that may originate from Schwann cells
or related cells of the perineural sheath (schwannomas and perineuriomas) or from
a combination of endoneurial, epineurial, or stromal fibroblasts (neurofibromas and
MPNSTs).[3]
[7] Difficulties in histologic differentiation and the overlapping biological behaviour
summarize these tumours in the general definition of PNSTs.[3]
[18]
Peripheral nerve sheath tumours develop mainly from peripheral nerves, but they may
extend along the nerve roots through the intervertebral foramen developing an EM component
or may even involve the spinal cord's grey matter (e.g. as dumbbell tumours).[3]
[19]
[20] Nevertheless, primary intraspinal–extradural PNSTs have been reported in dogs.[1]
[6]
[20] In people, tumours with an extraforaminal component seem to decrease in frequency
from the upper to the lower region of the spine. An explanation could be relatable
to the anatomic features of nerve roots that arise from the spinal cord at a nearly
right angle in the cervical vertebrae and at more acute angles in the lower spinal
tract, running longer distances within the vertebral canal to reach the intervertebral
foramina.[21] To the authors' knowledge, this is the first description in the dog of an ED PNST
with well-defined margins, located at T7-T8 level, and without any involvement of
osseous vertebral structures and intervertebral foramina. Also, as previously reported,
the median age of dogs with PNSTs was 7.7 years.[1]
[7] Therefore, our 2-year-old patient was relatively young compared with previous reports.
Neither gender nor breed predilection has been demonstrated.[1]
[5] Clinical signs are mainly related to the anatomical location and progressive spinal
cord compression, consistent with the clinical presentation of our case.[6]
The PNSTs are slow-growing, locally invasive and have a low rate of metastasis.[1] Nevertheless, a recent study on canine soft-tissue sarcomas reported an 11.1% (27/242
cases) frequency of metastasis of PNST.[22] In general, lungs and regional lymph nodes are the most common site for metastasis
of soft tissue sarcomas[23]; there was no metastasis detectable in the present case. As for all neoplasms, early
recognition is essential in PNSTs as well. Diagnosis often requires advanced imaging
techniques,[16]
[24] such as CT and MRI. The PNST of this report had on MRI an appearance similar to
cases described before but showed some unusual characteristics, such as being ED and
located in the mid-thoracic spinal region, entirely within the vertebral canal.
Complete surgical excision of PNSTs is associated with significantly improved survival
in both animal and human patients.[1]
[5]
[6] The final prognosis depends upon the degree of local resection, degree of spinal
infiltration, direct damage to the spinal cord by the lesion itself or during surgical
manipulation, surgeon's experience, and tumour type.[6] Extradural tumours are removed by laminectomy, either dorsal or by hemilaminectomy,
via blunt or sharp dissection. General surgical oncologic principles, like wide surgical
margins, are often not feasible in neurosurgical oncology because of the obvious vital
nature of the surrounding nervous system.[1]
[5] The ‘en bloc’ resection reduces the risk of local recurrence and results in prolonged
survival; on the contrary, incomplete resection resulted in tumour recurrence and
fatal outcome.[9] Local excision was performed, but wide surgical margins obviously were not achievable
in our case.
The beneficial effect of SRT in terms of survival is reported,[1]
[10]
[13] despite additional survival time was noted only adding SRT when recurrence was noted.[1]
[25] Therefore, surgery remains the treatment of choice.[1] Despite aggressive and timely management, the overall prognosis is considered poor
for most cases of PNSTs. In several cases, dogs were euthanatized because of worsening
of clinical signs or in instances because of owner's decision not to treat.[3]
[5]
[7]
[20]
[26] Furthermore, survival time for PNSTs managed surgically ranged from 10 days to 18
months with a median survival time of 5 months,[5] and in a recent retrospective multicentre case series, median survival time was
187 days (6.2 months).[1] However, comparison of survival time after surgery is difficult because in these
reports, several cases of recurrence were treated with SRT.[1] Nevertheless, these reports are similar to what was previously described for 12
cases of spinal PNSTs with a median survival time of 180 days.[27] Conversely, dogs that underwent hemilaminectomy with rhizotomy for PNST survived
for only 2 or 3 months, according to another recent report.[6] Inconsistent data exist on recurrence of spinal PNST. One study reported a median
relapse-free interval of 108 days postoperatively in 7 of 13 dogs treated with surgery
alone.[1] Another study on 23 dogs showed recurrence at 1 month (0–14 months)[5]; conversely, recurrence was noted at 7 months after surgery in two recent case reports.[14]
[19] Our patient did not show recurrence of clinical signs within 18 months (540 days)
after treatment, and the absence of local recurrence seemed to be confirmed by the
CT scan 13 months (390 days) after surgery.
Macroscopical and histological features of the mass described reflect what was previously
reported.[6]
[7]
[20]
[24] The diagnosis of PNST in our case was confirmed by histopathological examination
and immunohistochemical labelling. Immunohistochemistry revealed that the neoplasm
was immunoreactive for vimentin, GFAP, and S-100 protein but was immunonegative for
anti-laminin antibody. In a previous study, only 33.3% of PNSTs had positive immunoreactivity
against this marker.[28] The positive result for vimentin confirmed that the tumour was of mesenchymal origin,
while meningioma, fibrosarcoma, and lymphosarcoma were excluded by the positive reaction
to S-100. Moreover, a positive result for GFAP and the low number of mitotic figures
were consistent with benign behaviour.[29] Fibrous meningiomas may resemble schwannomas, and the whorl formation in transitional
meningiomas can mimic that of schwannomas. However, meningiomas are S-100 negative
and can be distinguished ultrastructurally by their characteristic interdigitating
cellular processes, prominent desmosomal and gap junctions, and lack of a basal lamina.[30] Although rhabdomyosarcomas and hemangiopericytomas can be positive to S-100, they
show only focal immunoreactivity for S-100 and usually involve less than 20% of the
cells.[29]
This case represents, to the best of our knowledge, the first report in a dog with
a primary ED PNST in the T7-T8 location; also, the dog was much younger than others
with spinal PNSTs reported so far, was successfully treated by surgical excision alone
and had a relapse-free outcome of at least 18 months.
Peripheral nerve sheath tumours should be considered in the differential diagnosis
of dogs showing an intraspinal ED mass without any signs of extension through a neuroforamen
on advanced imaging.
