Zoster Laryngitis with Multiple Cranial Nerve Palsy Progressed as Ascending Involvement
Article information
Abstract
Background
Herpes zoster of the head and neck commonly presents with Ramsay Hunt syndrome. However, vesicular eruptions may occur on the pharyngeal or laryngeal area with multiple lower cranial-nerve (CN) palsy.
Case Report
We report on the case of a 54-year-old man with herpes zoster of the pharynx and larynx with multiple CN palsy and persistent hiccups. He initially developed progressive dysphagia, hoarseness, and persistent hiccups (CN IX and X). After admission, Dizziness, hearing impairment, and peripheral facial palsy (CN VII and VIII) were complicated. The results of a polymerase chain reaction test of saliva and vesicular fluid from the ear and throat were strongly positive for varicella zoster virus. The progression of CN palsy was in an ascending sequence.
Conclusion
We suggest that the sequence of CN palsy may be either ascending or descending, depending on the initial site of involvement.
INTRODUCTION
Herpes zoster of the head and neck commonly presents with Ramsay Hunt syndrome (RHS) [1-3]. However, vesicular eruptions may occur on the pharyngeal or laryngeal area with multiple lower cranial-nerve (CN) palsy [1-10], meningoencephalitis, and vasculopathy. We herein report a case of RHS with vesicles in the pharynx and larynx, complicated by multiple lower CN palsy and persistent hiccups in an immunocompetent patient.
CASE REPORT
A 50-year-old man presented with a 3-day history of progressive dysphagia, hoarseness, fever, and persistent hiccups. He also complained of facial pain on the right side. He had been healthy until three days prior to admission. He had a history of chickenpox in his childhood and recently had had severe emotional distress.
Upon presentation, blood pressure was 130/80 mmHg and body temperature was 39.2°C. Physical examination revealed multiple small vesicles over the cheek, ear, oral cavity, and pharynx on the right side. There was paralysis of the soft palate and reduced gag reflex on the right side. However, he had no meningeal irritating signs, facial palsy, hearing loss, tongue deviation, or weakness of the sternocleidomastoid and trapezius muscles. The result of a Tzanck test of the vesicles was positive. Initial brain magnetic resonance imaging (MRI) showed no abnormality. He was diagnosed with herpes zoster with CN IX and X palsy. We started intravenous acyclovir (30 mg/kg/day) and dexamethasone (20 mg/day) for herpes zoster, and oral valproic acid and topiramate for intractable hiccups.
On the next day, his hoarseness became worse. Because he could not swallow food or fluid due to severe dysphasia, we started tube feeding. Laryngeal fibroscopy disclosed multiple vesicles and ulcers on the larynx, pharynx, epiglottis, and vocal cord palsy at the right side (Fig. 1). Laboratory tests showed a white blood cell count of 8,460/mm3 with 70.7% neutrophils, 13.7% lymphocytes, and 8.4% monocytes. C-reactive protein was significantly increased, with a concentration of 4.6 mg/dL (range, <0.06 mg/dL), and an erythrocyte sedimentation rate of 31 mm/h (range, <20 mm/h). Other routine laboratory investigations were within normal ranges. Varicella-zoster virus (VZV), immunoglobulin (Ig) G, and Ig M antibody were positive, 28.30 and 7.32, indicating reactivation of VZV. A serum polymerase chain reaction (PCR) test for VZV deoxyribonucleic acid (DNA) was weakly positive. However, the results of a PCR test of saliva and vesicular fluid from the ear and throat were strongly positive (Fig. 2). The patient was immunocompetent on laboratory investigations: hematological screening for Human immunodeficiency virus and lymphocyte subpopulations count, serum immunoglobulins, and complement C3 and C4.
Three days after admission, the patient developed dizziness, hearing impairment, and peripheral facial palsy on the right side. Hoarseness and dysphagia were aggravated. Neurological examination showed spontaneous left-beating nystagmus with delayed vestibulo-ocular reflex upon rightward head rotation. A caloric test disclosed a vestibulopathy and an audiogram revealed a mild sensory neural hearing loss in the right ear. On the fourth day, a follow-up MRI scan with enhanced contrast revealed an enlarged right facial nerve in the area adjacent to the right ear (Fig. 3). Fifth days after admission, dysphagia and hoarseness gradually improved. On the seventh day, facial palsy, dizziness, and hiccups were beginning to improve. After a total of a 14-day course of acyclovir and corticosteroid treatment, he was discharged in a much-improved state. After 15 months, he had mild facial palsy and hoarseness, but no hearing loss, dizziness, dysphagia, or hiccups.
DISCUSSION
Reactivation of the VZV is facilitated by diminution of specific cellular immunity to VZV, as happens during the ageing process or in immunosuppressive conditions, following emotional stress or recent viral infection [1,6]. The virus reactivates in the ganglionic neurons along the entire neuraxis and causes herpes zoster [6]. However, our patient proved immunocompetent based on laboratory investigations and had no history of immunosuppressive therapy or malignancy, only emotional stress. In the head and neck area, herpes zoster may occur in uncommon patterns, such as vesicular eruptions on the pharyngeal and laryngeal area with lower CN palsy, intractable hiccups, or facial pain without skin eruption [1-11]. We present a case of herpes zoster with vesicular eruptions on the pharyngeal and laryngeal area as well as the face, further complicated by intractable hiccups and multiple lower CN palsy, including CN VII, VIII, IX, and X.
Case reports of multiple lower CN involvement due to RHS have rarely been described; zoster laryngitis with cranial polyneuropathy [1-4,6-10], and herpes zoster with CN VII, VIII, and X palsy in an immunocompetent patient [5]. However, there has been no case report of pharyngeal and laryngeal zoster, similar to our patient, complicated by multiple CN palsy and persistent hiccups in the literature. Only a case of multiple CN palsy and persistent hiccups without vesicular eruption was reported [11].
The pathogenic mechanism of multiple CN palsy in herpes zoster has not been clearly elucidated. There have been reports about communication of lower CNs [12-14]. Recently it was reported that there are various communications among CN branches around the acoustic meatus and the auricle before reaching the central nervous system; CN X had communications with the CN VII and IX [15]. We suggest that through these anatomical communications, VZV can spread to neighboring CNs and cause multiple CN palsy. In our case, he developed dysphagia, hoarseness, and persistent hiccups (CN IX and X) initially, then hearing impairment and facial palsy (CN VII and VIII) after admission.
CN involvement was distinctive as a progressive and ascending sequence, starting from CN IX and X, then spreading to CN VII and VIII. In the previous case reports, the sequence of CNs was variable, ascending [1,2,11], descending [4,10], or not exactly described [3,5]. So we suggest that the sequence of CN palsy depends on the initial site of CN involvement. Then the VZV spreads to adjacent CNs through anatomical communications, either ascending or descending. Patient with herpes zoster with hoarseness and bulbar palsy may develop RHS and vice versa. For this reason, physicians should pay attention to the possibility of the progression of CN palsy for patients with bulbar palsy or facial palsy.
Because cases of laryngeal and pharyngeal herpes zoster with multiple CN palsy and persistent hiccups are uncommon, it is important to rule out other causes of multiple CN palsy. CN involvement in herpes zoster may progress to adjacent CNs through anatomical communications among CNs. We suggest that the sequence may be either ascending or descending, depending on the initial site of involvement. For this reason, physicians should pay attention to possibility of the progression of CN palsy.
Notes
The authors have no funding, financial relationships, or conflicts of interest to disclose.
Acknowledgements
The authors thank Se-Jin Lee for reviewing the manuscript.