A patient with typical Wallenberg syndrome: a case report and literature review - TMR Publishing Group
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CASE REPORT doi: 10.12032/TMRND20200603010 TMR Non-Drug Therapy A patient with typical Wallenberg syndrome: a case report and literature review Min Zhang1, Hong You1∗ 1 Sino-French Department of Neurological Rehabilitation, Gansu Provincial Hospital, Lanzhou 730000, China. *Corresponding to: Hong You. Sino-French Department of Neurological Rehabilitation, Gansu Provincial Hospital, No.204 Donggang West Road, Lanzhou 730000, China. E-mail: lzyouhonginedin@163.com. Highlights This case report extends knowledge of clinical characteristics of Wallenberg syndrome. Increases awareness of Wallenberg syndrome etiologies, diagnosis, and comprehensive management. It provides a new reference value for clinical application. Submit a manuscript: https://www.tmrjournals.com/ndt TMR | June 2020 | vol. 3 | no. 2 | 63
doi: 10.12032/TMRND20200603010 CASE REPORT Abstract Wallenberg syndrome is a special type of medulla oblongata infarction with many and severe clinical dysfunction, which is dorsolateral medullary syndrome. Wallenberg syndrome can have various initial symptoms due to different damaged parts. Typical clinical manifestations of the syndrome include dizziness, vomiting, dysphagia, cross sensory disturbance, ataxia, etc. Based on the complexity of functional anatomy, infarction in the medulla oblongata can produce various types of clinical symptoms or signs depending on the location. We describe the clinical comprehensive management of a 71-year-old man who presented with typical Wallenberg syndrome. Through early diagnosis and comprehensive clinical management, the prognosis of patient can be effectively improved. Keywords: Wallenberg syndrome, Management, Prognosis, Case report, Literature review Statement of ethics: The patient consented to the publication of this paper. This case report was approved by the Ethics Committee of Gansu Provincial Hospital. Acknowledgments: This study was supported by a grant from the Gansu Provincial Hospital in China (No. 18GSSY4-31). Abbreviations: MRI, magnetic resonance imaging; MRA, magnetic resonance angiography; PICA, posterior inferior cerebellar artery. Competing interests: The authors declare that there is no conflict of interest. Citation: Min Zhang, Hong You. A patient with typical Wallenberg syndrome: a case report and literature review. TMR Non-Drug Therapy 2020, 3 (2): 63–68. Executive editor: Rui-Wang Zhao. Submitted: 30 December 2019, Accepted: 17 April 2020, Online: 03 June 2020. TMR | June 2020 | vol. 3 | no. 2 | 64 Submit a manuscript: https://www.tmrjournals.com/ndt
CASE REPORT doi: 10.12032/TMRND20200603010 conscious, indwelling gastric tube for nasal feeding, Introduction poor sleep, no abnormality in stool and urine, and no obvious weight loss. Wallenberg syndrome is a special type of medulla He had a history of hypertension for more than 10 oblongata infarction with many and severe clinical years, with the highest hypertension being 190/100 dysfunction, which is dorsolateral medullary syndrome mmHg. He did not take medicine regularly and his [1, 2]. Typical clinical manifestations of the syndrome blood pressure was not monitored regularly. Denial of include dizziness, vomiting, dysphagia, cross sensory the history of diabetes, coronary heart disease and disturbance, ataxia, etc [3]. In terms of etiology of other chronic diseases, denial of the history of Wallenberg’s syndrome, middle-aged and elderly infectious diseases, denial of major surgery and trauma, patients mainly suffer from atherosclerosis, and young denial of blood transfusion history, denial of food and patients are mainly cardiac embolism. Common risk drug allergy history. The vaccination history is factors are the same as ischemic stroke, including unknown. More than 50 years of smoking history, hypertension, diabetes, hyperlipidemia, coronary heart denied the family history of genetic diseases. disease, atrial fibrillation, etc [4]. Analyses of lesions via magnetic resonance imaging (MRI) have revealed Physical examination (including rehabilitation that various types of clinical symptoms or signs may assessment) be present depending on the location of a lesion in the (1) Physical examination: T: 36.3°C, P: 68 times/min, medulla oblongata [5]. This article reports the clinical R: 17 times/min, BP: 150/90 mmHg. Clear mind, experience of comprehensive management of a typical normal development, moderate nutrition, wheelchair Wallenberg syndrome patient. pushed into the ward, physical examination cooperation, answer the right question, slurred speech. Case Presentation General physical examination showed no abnormality, while cardiopulmonary examination and abdominal Current medical history examination showed no abnormality. A 71-year-old man was admitted to hospital for (2) Rehabilitation assessment: clear mind, nasal “sudden dizziness with dysphagia and unstable feeding diet, slurred speech, bilateral nasolabial sulcus standing for 1 month”. One month ago, the patient basically symmetrical, tongue extension basically suffered from sudden dizziness at night, accompanied centered, uvula basically centered, pharyngeal reflex by unstable standing, unconscious loss at that time, no weakened, soft palate raised poorly, left side obvious. nausea, vomiting and other discomfort. Then the No obvious abnormality is found in muscle strength patient was rushed to the local county hospital. The and muscle tension of limbs. The left facial numbness, blood pressure was measured at 190/100 mmHg and right limb pain and temperature sensation decreased, no obvious abnormality was found in cranial CT at that limb tendon reflex was normal and pathological sign time, and the dizziness symptom of patient was was negative. Bilateral finger-nose test and relieved after antihypertensive treatment. The patient heel-knee-shin test are satisfactory, but the left side is returned home for recuperation. Next morning, the slightly worse. The mini-mental state examination patient suffered from dizziness again, accompanied by score was 26 points. Balance check does not cooperate dysphagia, nausea, vomiting, general weakness, (dizziness cannot cooperate), Watian drinking water unstable standing, etc., and then had blurred test grade 5, assessment of daily living ability score consciousness. Therefore, he called for emergency (Modified Barthel Index): 45 points, severe functional medical help and was admitted to Gansu Provincial defect. Hospital for treatment. No bleeding focus was found after cranial CT. Considering diagnosis of “cerebral Laboratory and imaging examination infarction”, he was treated with blood circulation (1) Laboratory examination: routine blood, urine and promotion, microcirculation improvement, antiplatelet, feces, coagulation function, blood sugar, electrolyte of lipid regulation, stomach protection, dehydration and liver and kidney function and blood lipid are basically intracranial pressure reduction. The cranial MRI normal. (2) Imaging examination: cranial MRI, left examination revealed left medulla oblongata infarction. medulla oblongata acute infarction (Figure 1); cranial Pulmonary infection occurred during hospitalization, magnetic resonance angiography (MRA), left vertebral aspiration pneumonia was considered, and the patient artery not shown (Figure 2). The whole brain digital improved after indwelling gastric tube and substraction angiography examination was rejected by anti-infection treatment. At present, there are still patient. dizziness and discomfort, dysphagia, unstable standing and other functional disorders. For further Diagnosis rehabilitation treatment, we have admitted the patient (1) Clinical diagnosis: ① brain stem infarction to our department with “brainstem infarction (medulla convalescence (left medulla oblongata), ② oblongata)”. At the time of admission, the patient was hypertension grade 3, extremely high risk. According Submit a manuscript: https://www.tmrjournals.com/ndt TMR | June 2020 | vol. 3 | no. 2 | 65
doi: 10.12032/TMRND20200603010 CASE REPORT to the patient’s medical history and imaging findings, syndrome. Furthermore, it is considered that the causes the diagnosis is clear. of this syndrome may be hypertension, smoking (2) Functional diagnosis: dysphagia, ataxia and history for many years, as well as the age is also a dysfunction of daily living. Watian drinking water test factor. grade 5, pharyngeal reflex weakened, etc., diagnosed as dysphagia. The left side of bilateral finger-nose test Differential diagnosis and heel-knee-tibia test is slightly worse, and the (1) Brain stem hemorrhage is usually more acute and diagnosis is ataxia. Modified Barthel Index score: 45 severe, usually coma occurs earlier, most patients are points, severe functional defect, diagnosed as critically ill, and the mortality rate is extremely high. dysfunction of daily living. Obvious hemorrhage foci can be seen in brain stem on (3) Clinical syndrome: Wallenberg syndrome. The cranial CT and can be clearly identified on imaging. (2) cranial MRI examination of this patient showed that Cerebral hemispheric infarction, such as basal ganglia, the left medulla oblongata infarction foci, and the usually starts with limb weakness, which can be patient had 4 major symptoms [2, 6, 7], including gradually aggravated or accompanied by dysphagia, dysphagia, ataxia, numbness of the affected lateral part, usually pseudobulbar paralysis and pharyngeal reflex. and decreased pain and temperature sensation of the Cranial MRI examination can clearly identify the healthy limb. The clinical diagnosis was Wallenberg infarct site. Figure 1 Cranial MRI shows left medulla oblongata infarction (black arrow indication) Figure 2 Cranial MRA shows left vertebral artery not shown (black arrow indication) TMR | June 2020 | vol. 3 | no. 2 | 66 Submit a manuscript: https://www.tmrjournals.com/ndt
CASE REPORT doi: 10.12032/TMRND20200603010 by vertebral artery dissection [10, 13, 14]. In patients Comprehensive management with dorsolateral medulla oblongata syndrome, only a few patients are caused by PICA occlusion. Most of After admission, patient was thoroughly evaluated the causes of PICA ischemia are stenosis or occlusion (liver function, renal function, electrolyte, prothrombin of intracranial segment or origin of vertebral artery, or time activity, blood routine , );monitor patient’s blood thrombus shedding at origin of vertebral artery [10, 15, pressure, and provide nasal feeding diet, and 16]. Cranial MRA of this patient showed a loss of left giveantihypertensive (amlodipine), antiplatelet vertebral artery signal. Although no further digital (aspirin), anti-vertigo (betahistine), and promotion of substraction angiography examination of the whole nerve repair (bossgate) treatments. brain was performed, it could still reflect that there For swallowing dysfunction, there are mainly basic were some problems in the vertebral artery. training, indirect swallowing training and feeding Considering that the responsible vessel for this training [8, 9]. Basic training includes sensory occurrence is the left vertebral artery, the etiological stimulation (including touch, temperature and taste type is macroatherosclerosis, and qualitative diagnosis stimulation) and muscle training of mouth and face. is ischemic cerebrovascular disease. Indirect swallowing training is to train patients to Wallenberg syndrome can have various initial swallow related decomposition actions under the symptoms due to different damaged parts, but condition of no eating, and to achieve the purpose of vertigo/dizziness is common in clinic [3]. Dizziness is safe and effective swallowing by means of some the first symptom of this patient, which indicates specific manipulations and actions. During the feeding vestibular nucleus is involved. Nausea and vomiting, training, choose the appropriate body position, and dysphagia, ataxia, and cross sensory disturbance select the appropriate one-mouthful food intake gradually appear as the disease progresses [17, 18]. At according to the actual swallowing function of the the initial stage of the disease, due to incomplete patient, and increase it according to the patient’s symptoms or careless physical examination, it is easy reaction during the training [8]. Electric standing bed to be misdiagnosed as posterior circulation ischemia, training can improve the patient’s adaptability to body delay relating examination and treatment, and even position changes, enhance the proprioceptive input and cause sudden death of patients due to respiratory or balance of lower limbs, and prevent complications. cardiac arrest. Exercise therapy and balance function training There are 8 types of Wallenberg syndrome sensory improve limb movement and coordination ability, and disturbance [19]: (1) lateral contralateral limb sensory improve balance and coordination functions; disturbance of lesion, which is crossed sensory occupational therapy improves patients’ coordination disturbance; (2) the pain and temperature sensation of ability and fine function, and improves their daily bilateral face and contralateral lesion decreased; (3) activities. sensory disturbance of the lesion to the lateral part and After nearly one month of rehabilitation treatment, hemi-body; (4) sensory disturbance only at the lateral the patient’s swallowing function was significantly part of the lesion; (5) somatosensory disturbance on improved. The Watian drinking water test was grade 2. opposite side of lesion only; (6) bilateral The gastric tube was pulled out and the oral intake was somatosensory disorders; (7) bilateral facial sensory good. Sitting balance level 3, standing balance level 2. disturbance; (8) lesion-to-lateral sensory disturbance. Berg Balance Scale score: 31 points. Patient can walk Combined with the clinical symptoms and signs of this a short distance with the help of family members. patient, the type of sensory disturbance of this patient Modified Barthel Index score: 75 points, mild is analyzed as typical cross sensory disturbance. The functional defect. previous reports of patients with dorsolateral medulla oblongata syndrome presenting as pure sensory Discussion disturbance [20]. In addition, this patient has no consciousness disorder, but there are also patients with Wallenberg syndrome, also known as posterior inferior consciousness disorder, which may be caused by cerebellar artery (PICA) syndrome and dorsolateral gradual aggravation of edema after infarction, medullary syndrome, is the most common posterior compression of brainstem and influence on circulation ischemic stroke syndrome [2]. In 1895, cerebrospinal fluid circulation [21]. German neurologist Adolf Wallenberg described the If the patient lacks typical clinical manifestations, clinical manifestations of the syndrome. Of all some scholars suggest that the possibility of ischemic stroke patients, about 20% are posterior Wallenberg syndrome can be indicated when the circulation stroke, and about half of them can be patient meets the following two conditions: (1) cranial represented as syndrome, which is mostly male and is MRI indicates that the focus is in medulla oblongata, more common in the middle-aged and elderly and dysarthria and dysphagia must be one of them; (2) population [10–12]. About 75% of patients are caused cranial MRI indicates that the lesion is located at the by atherosclerosis, 17% by cardiac embolism, and 8% dorsolateral medulla oblongata, pain and temperature Submit a manuscript: https://www.tmrjournals.com/ndt TMR | June 2020 | vol. 3 | no. 2 | 67
doi: 10.12032/TMRND20200603010 CASE REPORT sensation disorder, ataxia and Horner syndrome must adult with cerebellar infarct. Acta Neurol Taiwan be one of them [22]. This patient met the above 2008, 17: 243–247. requirements and was diagnosed accordingly. 14. Sun H, Zhou Y, Bai C, et al. Clinical features and To sum up, this case extends our knowledge of etiology of Wallenberg syndrome. Chin J clinical characteristics of Wallenberg syndrome, and Gerontol 2005, 25: 382–383. increases awareness of its etiologies, diagnosis, and 15. Collado A, Santamaria J, Ribalta T, et al. comprehensive management, and effectively improves Giant-cell arteritis presenting with ipsilateral the prognosis of patient. hemiplegia and lateral medullary syndrome. Eur Neurol 1989, 29: 266–268. References 16. Tehrani ASS, Desanto JR, Kattah JC. Neuroimaging "HINTS" of the lateral medullary 1. Kim K, Lee HS, Jung YH, et al. Mechanism of syndrome. J Neuroophthalmol 2017, 37: 403–404. medullary infarction based on arterial territory 17. Arshad Q, Roberts RE, Ahmad H, et al. Patients involvement. J Clin Neurol 2012, 8: 116. with chronic dizziness following traumatic head 2. Day GS, Swartz RH, Chenkin J, et al. Lateral injury typically have multiple diagnoses involving medullary syndrome: a diagnostic approach combined peripheral and central vestibular illustrated through case presentation and literature dysfunction. Clin Neurol Neurosurg 2017, 155: review. CJEM 2014, 16: 164–170. 17–19. 3. Jia J. Neurology. Beijing: People’s Medical 18. Xu Z, Wang C, Li J, et al. Research progression Publishing House 2013. on dysphagia in patients with cerebralinfarction. 4. Hu J, Xu R, Lu X, et al. Clinical analysis of Chin J Rehabil 2017, 32: 148–150. Wallenberg’s syndrome. Chin J Contemp Neurol 19. Kim JS, Lee JH, Lee MC. Patterns of sensory Neurosurg 2019, 19: 41–46. dysfunction in lateral medullary infarction: 5. Ogawa K, Suzuki Y, Oishi M, et al. Clinical study clinical-MRI correlation. Neurology 1997, 49: of 46 patients with lateral medullary infarction. J 1557–1563. Stroke Cerebrovasc Dis 2015, 24: 1065–1074. 20. Yamaoka Y, Kishishita S, Takayama Y, et al. A 6. De Bruyn D, Van Aken E, Herman K. A rare case report of a case involving body lateropulsion with of concomitant sicca keratopathy and ipsilateral numbness of the ipsilesional fingers caused by a central facial palsy in Wallenberg's dorsolateral small infarction in the dorsal part of the middle medullary syndrome. GMS Ophthalmol Cases medulla. Case Rep Neurol 2018, 10: 54–59. 2017, 7: Doc08. 21. Lee SH, Kim JS. Acute diagnosis and 7. Aydogdu I, Ertekin C, Tarlaci S, et al. Dysphagia management of stroke presenting dizziness or in lateral medullary infarction (Wallenberg’s vertigo. Neurol Clin 2015, 33: 687–698. syndrome): an acute disconnection syndrome in premotor neurons related to swallowing activity? Stroke 2001, 32: 2081–2087. 8. Rosenvinge SK, Starke ID. Improving care for patients with dysphagia. Age Ageing 2005, 34: 587–593. 9. Battel I, Koch I, Biddau F, et al. Efficacy of botulinum toxin type-A and swallowing treatment for oropharyngeal dysphagia recovery in a patient with lateral medullary syndrome. Eur J Phys Rehabil Med 2017, 53: 798–801. 10. Kim JS. Pure lateral medullary infarction: clinical-radiological correlation of 130 acute, consecutive patients. Brain. 2003, 126: 1864–1872. 11. Kameda W, Kawanami T, Kurita K, et al. Lateral and medial medullary infarction: a comparative analysis of 214 patients. Stroke 2004, 35: 694–699. 12. Ma N. Analysis of clinical and imaging features of cerebral infarction in patients with posterior circulation. Guide China Med 2015, 10: 50–51. 13. Jao T, Liu HM, Tang SC, et al. Dissection of the posterior inferior cerebellar artery in a young TMR | June 2020 | vol. 3 | no. 2 | 68 Submit a manuscript: https://www.tmrjournals.com/ndt
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