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Оглавление14 Facial paralysis and facial spasm
Paralysis of the muscles of facial expression, or facial paralysis, is a very common problem in large animals with neurologic disorders and is a common part of the syndromes caused by temporohyoid osteoarthropathy.1–3 Dysfunction of the somatic efferent fibers of the facial nerve produces decreased spontaneous and reflex movements of the ear, eyelids, lips, and external nares. The ear, upper eyelid, and lips on the side of the lesion droop and the muzzle tends to be pulled to the opposite side with a unilateral lesion, making it usually easy to recognize in horses (Figure 14.1). This is less so in other species that tend to have little facial expression, naturally stiff or droopy ears and firm muzzles. However, when quite mild and when the patient is excited, facial muscle tone can be remarkably normal so that the syndrome may be very subtle to observe. In this situation, returning to observe the patient during a resting state, or use of mild sedation, can help uncover the signs. Ptosis of the upper eyelid is a feature of facial paralysis in all large domestic animals and is prominent in horses. It is due to the paralysis of the strong levator anguli oculi medialis muscle in these species that is innervated by the facial nerve CN VII. It is possible that the bulk of atonic supraorbital muscles and the paralysis of the frontalis muscle also contribute to the ptosis. Unfortunately, when upper eyelid ptosis is seen in large animals, the immediate thought is one of it being Horner syndrome (Figure 10.4). However, facial paralysis is vastly more common than sympathetic denervation of the eyelids in large animals and always must be considered the most likely cause.
Figure 14.1 Total left facial paralysis is seen in this horse (A) suffering from direct penetrating trauma to the base of the cranium including the left middle and inner ears. The horse in (B) suffered direct injury to the buccal branches of the left facial nerve resulting in mild deviation of the muzzle to the right.
Parasympathetic visceral efferent fibers pass with the somatic fibers to exit the brainstem, pass through the internal acoustic meatus, and then leave the main facial nerve within the facial canal to innervate the lachrymal gland (and palatine and nasal glands) via the major petrosal nerve and pterygoid ganglion.4 When these parasympathetic fibers in the facial nerve are damaged, then the loss of lachrymal tear production ensues resulting in keratoconjunctivitis sicca.
Damage to the central motor pathways in the frontal cortex, internal capsule, crus cerebri, and brainstem that control the facial nucleus and nerve can result in abnormal facial expression (Figure 14.2). This occurs without flaccid facial paralysis. There is still tone in the muscles of facial expression, and facial reflexes (CN V sensory → CN VII motor) are intact and may even be hyperactive. However, the expression may be bland or grimacing on one or both sides. Needle electromyographic examination of the facial muscles does not reveal denervation because the facial motor nucleus and nerve are still intact. Large, focal cerebral lesions such as hematoma, S. neurona encephalitis, and abscess have produced such signs of supranuclear facial motor dysfunction that, unlike in humans, appear to be ipsilesional, at least to the muzzle and lips of the distal face.
Trauma and bacterial infection of the middle and inner ears are the commonest cause of peripheral facial nerve paralysis,5–9 most particularly in young patients. With distal, peripheral facial nerve involvement, usually one or two branches of the nerve, not all three nerve branches (auricular, palpebral, and buccal), are involved. Pressure on the side of the face as a result of a tight halter or from recumbency damages buccal branches, paralyzing just the nares and lips; however, the ear and upper eyelid may droop because of separate but direct auricular and palpebral nerve trauma. Brainstem lesions, particu larly those caused by equine protozoal myeloencephalitis and listeriosis, can selectively involve facial nuclei in the brainstem and can mimic a peripheral lesion by producing selective, partial facial paresis. Neuritis of polyneuritis equi and equine Lyme neuroborreliosis are causes of unilateral facial paresis,10–12 and proliferative inflammatory lesions in and around the facial nerves of calves may be the result of partly treated and chronic bacterial otitis.13–16
Figure 14.2 In comparison to facial weakness, these two horses (A and B) have, at times, very good tone and movement in their face but at rest have a bland facial expression (A). Sometimes with voluntary effort and with facial reflex testing, their face shows hypertonic expression and hyperreflexia (B). Both horses had lesions in the forebrain without facial nuclear or facial nerve involvement. The first (A) had a vascular lesion involving much of the left forebrain, and the second had thalamic lesions of equine protozoal myeloencephalitis on the left side. It does appear that the distal facial, functional abnormalities as seen in these horses are ipsilesional to the damage to the central motor pathways to the facial nuclei.
Figure 14.3 Facial paralysis is seen as marked loss of facial expression and movement with drooping of the ear, and upper eyelid, and of the lips (A and B). Bilateral facial weakness seen here can be less evident due to the relative facial symmetry present (B). Collapse of alar folds with inspiratory restriction (A) occurs far more with bilateral than unilateral paralysis in horses. Also, mild degrees of facial paresis can be difficult to see especially in patients such as calves and piglets that do not normally have prominent facial expression and facial muscle tone. Re‐examination when a patient is fully relaxed or sedated can help determine degrees of partial facial weakness. Palpating for decreased muscle tone and observing and palpating for reduced facial reflexes are also very useful to confirm degrees of facial paresis.
Large animals accommodate to unilateral facial paralysis very well, but bilateral facial paralysis (Figure 14.3) results in difficulty in prehending food and in keeping it in the mouth. Horses with this syndrome do sequester food in the flaccid cheek pouches and drop a lot of food while eating. Temporary tarsorrhaphy may help alleviate damage to the cornea from the lack of tears, but permanent facial paralysis may necessitate enucleation of the eyeball because of keratitis sicca and exposure ophthalmitis.3 Exercising horses may require false nostril surgery as a result of an obstruction to inspiratory airflow.17 Chronic paralysis with muscle atrophy and fibrous contracture of the face can cause twisting of the muzzle and nares back across the midline toward the paralyzed side.
In the early phase of irritative lesions such as bacterial meningitis, viral meningoencephalitis, neuritis, and focal trauma involving the facial nerve, facial muscles can twitch and even remain in spasm prior to paresis or paralysis that may ensue. True, permanent hemifacial spasm with constant contraction of facial muscles, that relaxes following facial nerve anesthesia or general anesthesia as seen in humans and dogs does not yet appear to be recorded in large animals. This might be expected to occur following recovery from bacterial otitis media. As occurs in many other regional muscle groups,18 facial muscles are occasionally seen to undergo repetitive contraction described as facial tic or myoclonus. Some of these syndromes wax and wane, and one facial tic in a horse has been seen to become almost violent when hypocalcemia associated with systemic illness occurred, to then quieten with IV calcium treatment. The underlying cause for facial and other localized myoclonia is notoriously not found.18–20
Brainstem auditory evoked potential recordings may be used as proxy for facial nerve function as the facial nerve is intimate with the vestibulocochlear nerve for their course in the region of the temporal bone and its middle and inner ear compartments.21,22
References
1 1 Espinosa P, Nieto JE, Estell KE, Kass PH and Aleman M. Outcomes after medical and surgical interventions in horses with temporohyoid osteoarthropathy. Equine Vet J 2017; 49(6): 770–775.
2 2 Walker AM, Sellon DC, Cornelisse CJ, et al. Temporohyoid osteoarthropathy in 33 horses (1993–2000). J Vet Intern Med 2002; 16(6): 697–703.
3 3 Myrna KE. Neuro‐ophthalmology in the Horse. Vet Clin North Am Equine Pract 2017; 33(3): 541–549.
4 4 de Lahunta A, Glass E and Kent M. Veterinary Neuroanatomy and Clinical Neurology. 4th ed. Saunders, Elsevier, St. Louis, MO. 2015.
5 5 Gosselin VB, Francoz D, Babkine M, et al. A retrospective study of 29 cases of otitis media/interna in dairy calves. Can Vet J 2012; 53(9): 957–962.
6 6 Lamm CG, Munson L, Thurmond MC, Barr BC and George LW. Mycoplasma otitis in California calves. J Vet Diagn Invest 2004; 16(5): 397–402.
7 7 Francoz D, Fecteau G, Desrochers A and Fortin M. Otitis media in dairy calves: a retrospective study of 15 cases (1987 to 2002). Can Vet J 2004; 45(8): 661–666.
8 8 Katz L. Left otitis media/interna and right maxillary sinusitis in a Percheron mare. Vet Clin North Am Equine Pract 2006; 22(1): 163–175.
9 9 Ragle CA. Head Trauma. Vet Clin North Am Equine Pract 1993; 9(1): 171–183.
10 10 Vatistas N and Mayhew IG. Differential diagnosis of polyneuritis equi. In Practice 1995; 17: 26–29.
11 11 Vatistas NJ, Mayhew IG and Whitwell KE. Polyneuritis equi: a clinical review incorporating a case report of a horse displaying unconventional signs. Prog Vet Neurol 1991; 2: 67–72.
12 12 Johnstone LK, Engiles JB, Aceto H, et al. Retrospective evaluation of horses diagnosed with neuroborreliosis on postmortem examination: 16 cases (2004–2015). J Vet Intern Med 2016; 30(4): 1305–1312.
13 13 Jensen R, Maki LR, Lauerman LH, et al. Cause and pathogenesis of middle ear infection in young feedlot cattle. J Am Vet Med Assoc 1983; 182(9): 967–972.
14 14 Maenhout D, Ducatelle R, Coussement W, et al. Space occupying lesions of cranial nerves in calves with facial paralysis. Vet Rec 1984; 115(16): 407–410.
15 15 Van der Lugt JJ and Jordaan P. Facial paralysis associated with space occupying lesions of cranial nerves in calves. Vet Rec 1994; 134(22): 579–580.
16 16 McFadden AM, Mackereth GF, Avery MI, et al. A syndrome of facial paralysis of dairy calves in the Franklin district of New Zealand. N Z Vet J 2009; 57(1): 63–68.
17 17 Torre F. Use of autogenous cartilage graft from auricular cartilage in treatment of unilateral paralysis of nostril in racing standardbred horse. Equine Vet Educ 2003; 15(1): 10–14.
18 18 Beech J. Forelimb tic in a horse. J Am Vet Med Assoc 1982; 180(3): 258–260.
19 19 de Lahunta A, Glass EN and Kent M. Classifying involuntary muscle contractions. Comp Cont Ed Pract Vet 2006; 28: 516–529.
20 20 Kerby MJ. Repetitive facial nerve stimulation in a cow. Vet Rec 2006; 158(12): 420.
21 21 Wrzosek M, Niezwiedz A, Giza E, Borowicz H and Nicpon J. Auditory brainstem evoked response (BAER) in the diagnosis of nervous system diseases in horses. Medycyna Weterynaryjna 2012; 68(9): 557–561.
22 22 Aleman M, Puchalski SM, Williams DC, Kass PH and Holliday TA. Brainstem auditory‐evoked responses in horses with temporohyoid osteoarthropathy. J Vet Intern Med 2008; 22(5): 1196–1202.
