An unexpected case of Ramsay hunt syndrome: case report and literature review
BMC Research Notes volume 6, Article number: 337 (2013)
Ramsay Hunt Syndrome (RHS) is a rare, severe complication of varicella zoster virus (VZV) reactivation in the geniculate ganglion. Facial paralysis is one of the features and without treatment, it fully recovers in as little as 20% of cases; this is much improved if treatment is started within 72 hours. This case is noteworthy in that coexistence of facial palsy with cervical dermatome involvement by VZV is not typical of RHS. Yet, it has been reported before.
A 54 year old Caucasian woman presented with right ear discomfort, difficulty hearing and a vesicular rash along the pinnae, 8 days after the eruption of a similar rash in the right C2-C4 dermatomes. 2 days later, she awoke with a partial right-sided facial paralysis, which improved with treatment (valacyclovir and prednisone).
This case is most pertinent to Family Practice, Otolaryngology and Neurology. It highlights the possible co-existence of RHS with cervical VZV reactivation and encourages physicians to monitor for this complication even before geniculate ganglion reactivation occurs. RHS is a rare disease that can present with vague symptoms. A high index of suspicion and close follow up are essential. Early intervention with antivirals and corticosteroids has shown significantly improved outcomes in these patients.
Ramsay Hunt Syndrome (RHS), also called Herpes Zoster Oticus, is a rare, severe complication of varicella zoster virus (VZV) reactivation. The classic triad consists of otalgia, vesicles in the auditory canal and ipsilateral facial paralysis. Without treatment, full recovery of the facial paralysis occurs in as little at 20% of cases; this is much improved if treatment is started within 72 hours. The risk of RHS in VZV reactivation has been quoted as little as 0.2% at day 60. However, the long-term morbidity that may result from RHS makes this an important topic of discussion. This case is noteworthy in that coexistence of facial palsy with cervical dermatome involvement of VZV is not typical of RHS. The aim of this article is to inform physicians about the presentation, including atypical, and management of RHS in order to facilitate prompt diagnosis, treatment and appropriate specialist referral.
A 54-year-old Caucasian female, with no past medical history, developed right-sided neck pain on day 1. On day 4, an erythematous, vesicular rash erupted at the site of pain. She was diagnosed with contact dermatitis at a walk-in clinic. Over days 4–9, she developed a right earache and headache and the rash spread to her upper right chest-wall. The rash was described as “dull and achy with intermittent sharp pain”. On day 9, at the family doctor’s office, exam showed an erythematous, vesicular eruption on the right anterior chest, neck and shoulder (C2, C3 and C4 dermatomes). The rash halted at the midline (Figure 1). It was tender, warm and blanched when palpated. The patient was diagnosed with herpes zoster (HZ) and secondary cellulitis. Valacyclovir, cephalexin and acetaminophen were started. On day 12, she returned with right ear discomfort and difficulty hearing. Exam showed a similar rash along the auricle but the external auditory canal was normal. Nortryptyline was started for neuralgia. On day 14, she woke up with partial right-sided facial paralysis. In the Emergency Room, RHS was diagnosed. Valacyclovir was extended to 10 days and prednisone started. A neuro-ophthalmology referral was made. On day 46, the patient returned showing significant improvement. She could smile symmetrically and close her right eye completely.
Epidemiology of RHS
The Center for Disease control estimates that 32% of people in the USA will have HZ during their lifetime. The most important risk factor is increasing age. RHS has a much lower incidence, presenting in only 0.2% of all HZ cases[3, 5]. After primary VZV infection, the virus can remain dormant in sensory dorsal root ganglia. Reactivation causes HZ (shingles) - a painful, ipsilateral, vesicular eruption in a limited dermatomal distribution. Pain may precede the vesicles. In RHS, VZV reactivates in the geniculate ganglion, causing peripheral facial paralysis, otalgia and auricular vesicles. Late diagnosis is common. The vesicles may appear after facial paralysis in a minority of cases (14% of cases in the only prospective study done). This means that a proportion of patients diagnosed with Bell’s palsy actually have RHS sine herpete. Cervical involvement of herpes zoster is rare with RHS and therefore makes this case one of special interest. As RHS is a reactivation of VZV in the geniculate nucleus, the etiology of co-existent cervical dermatome involvement is not well understood. Three theories have been hypothesized. One such theory is that of cerebrospinal fluid (CSF)/hematogenous spread. In one study, pleocytosis in the CSF was seen in 38% of cutaneous herpes zoster cases. Moreover, Haanpaa et al. isolated VZV in the CSF of 21% of patients with cutaneous lesions, but without meningeal or encephalitis symptoms. Additionally, viremia is a common occurrence during zoster. Since VZV has been documented in both blood and CSF during herpes zoster, these routes of spread could account for co-existent multi-dermatome involvement in HZ. Another theory is interneuronal communication. Brown et al. have shown that the second to fourth cervical nerves of the cervical plexus interconnect with peripheral branches of the facial nerve in some individuals. Numerous interconnections between the lower cranial nerves and upper cervical nerves have also been illustrated. These linkages are highly variable amongst individuals. It is plausible that VZV and associated inflammation may spread from a primary site of reactivation, through these anastomoses. Finally, the simultaneous activation of multiple ganglia may occur and could account for this clinical picture. Physicians should assess for immunocompromised states when patients present with multi-dermatomal VZV reactivation.
Diagnosis of RHS
Ramsay Hunt Syndrome is diagnosed clinically and is based on unilateral facial weakness plus vesicular lesions in the ipsilateral ear, hard palate or anterior 2/3 of the tongue. Facial weakness is identified by facial drooping, a widened palpebral fissure and decreased smile on the affected side (Figure 2). The associated pain is described as dull and aching with associated allodynia. Otalgia or vertigo completes the triad picture of RHS. The individual symptoms of RHS are non-specific and can be seen in other diseases; the differential is described in Table 1. Some 2-23% of unilateral facial palsies without vesicles are actually herpes zoster sine herpete. Therefore lesions are not required for diagnosis of RHS. The traditional diagnostic triad of RHS cannot be applied to the atypical presentations of RHS, including multiple nerve involvement as seen in this case. The use of CSF analysis or MRI adds no additional diagnostic value. Finally, the gold standard for diagnosing VZV reactivation is polymerase chain reaction of skin, saliva or middle ear fluid samples but this is rarely done clinically.
Complications of RHS
Corneal abrasions and ulcers, if eye-lid closure is impaired
Secondary infection with bacteria (cellulitis)
Postherpetic neuralgia, as with other Varicella Zoster virus reactivations
Permanent facial paralysis
Long term ipsilateral hearing loss and tinnitus
Management of RHS
Pharmacologic treatment of HZ complicated by RHS is controversial and requires ongoing research. Antivirals and corticosteroids are the current mainstay of treatment. Acyclovir, valacyclovir and famcyclovir have been shown to reduce the duration of acute HZ symptoms and associated long-term nerve damage. These drugs are well tolerated and are Food and Drug Administration (FDA) approved first line therapies for HZ. They are also used in RHS. In addition, the potent anti-inflammatory effect of steroids has been argued to enhance recovery in RHS by reducing the inflammation and edema of the facial nerve, thus reducing damage.
There is a paucity of published data on the efficacy of corticosteroids in RHS specifically. A Cochrane Review found no randomized controlled trials investigating the use of corticosteroids as in Ramsay Hunt syndrome. Yet, large RCTs showed that adjunct corticosteroids resulted in quicker healing of the rash and decreased incidence and severity of pain during HZ. Yet, there was no reduction in the incidence or severity of post herpetic neuralgia in these studies[20, 23].
Steroids and antivirals
A Cochrane Review of the sole randomized controlled trial (RCT) comparing treatment with antivirals and corticosteroids to corticosteroids alone in 15 RHS patients showed no significant difference in outcomes. A subsequent meta-analysis of 12 RHS articles concluded that antiviral therapy plus steroids compared to steroids alone significantly improved facial nerve function recovery (odds ratio of 2.8, 95% Confidence Interval (CI)).
The largest RHS treatment study was a retrospective analysis of 80 cases. Patients treated with acyclovir and prednisone within 72 hours of symptom onset had a complete recovery rate of 75% vs those treated after 7 days, who had a complete recovery rate of 30%. In addition, 50% of patients who were not treated in the first 3 days went on to have a complete loss of response to facial nerve stimulation.
Eye patches, taping the eye closed, artificial tears and oral analgesics are also used in the management of RHS.
Despite the absence of RCTs on RHS management, when considering the possibility of lifelong facial paralysis and hearing loss, experts recommend combination antiviral and corticosteroid therapy within the first 72 h of symptoms[6, 16]. Though no set-dosing regimen exists, 800 mg acyclovir 5 times/day for 7–10 days and Prednisone 1 mg/kg for 5 days and taper is used in published trials. In our case, acyclovir was replaced by 1 g valacyclovir TID for 10 days, with successful outcomes.
Ramsay Hunt syndrome is a rare disease that can present with vague symptoms and atypical presentations as seen in this case with cervical dermatome involvement. A high index of suspicion and close follow up are essential in patients who have HZ symptoms. Early intervention with antivirals and corticosteroids has shown to significantly improve outcomes in these patients.
Written informed consent was obtained from the patient for publication of this Case report and any accompanying images. A copy of the written consent is attached, for review by the Editor of this journal.
Mali Worme is a fourth year medical student at McGill University in Montreal, Quebec. She completed her Bachelor’s degree in Physiology and International Development Studies in 2010 at McGill University.
Dr Reena Chada is a family physician practicing in mid-town Toronto, Ontario. She completed her undergraduate medical training at the Michael G. DeGroote School of Medicine at McMaster University in Hamilton, Ontario followed by a residency program in Family Medicine at the University of Toronto in Toronto, Ontario.
Lilia Lavallee is a fourth year medical student at McGill University in Montreal, Quebec. She completed her Bachelor’s degree in Physiology in 2010 at McGill University.
Food and drug administration
Randomized controlled trial
Ramsay hunt syndrome
Three times per day
Varicella zoster virus.
Adour KK: Otological complications of herpes zoster. Ann Neurol. 1994, 35 (Suppl 1): 62-64.
Murakami S, Hato N, Horiuchi J, Honda N, Gyo K, Yanagihara N: Treatment of Ramsay hunt syndrome with acyclovir-prednisone: significance of early diagnosis and treatment. Ann Neurol. 1997, 41 (3): 353-357. 10.1002/ana.410410310.
Galil K, Choo PW, Donahue JG, Platt R: The sequelae of herpes zoster. Arch Int Med. 1997, 157 (11): 1209-1213. 10.1001/archinte.1997.00440320105010.
Harpaz R, Ortega-Sanchez IR, Seward JF: Prevention of herpes zoster: recommendations of the advisory committee on immunization practices (ACIP). MMWR Recomm Rep. 2008, 57: 1-30.
Yawn BP, Saddier P, Wollan PC, St Sauver JL, Kurland MJ, Sy LS: A population-based study of the incidence and complication rates of herpes zoster before zoster vaccine introduction. Mayo Clin Proc. 2007, 82 (11): 1341-1349. 10.4065/82.11.1341.
Sweeney CJ, Gilden DH: Ramsay hunt syndrome. J Neurol Neurosurg Psychiatry. 2001, 71 (2): 149-154. 10.1136/jnnp.71.2.149.
Ikeda M, Watanabe I: Ramsay Hunt syndrome associated with multiple cranial and/or cervical nerve involvement. Possible routes of dissemination of reactivated latent varicella zoster virus. New horizons in facial nerve research and facial expression. Edited by: Yanagihara N, Murakami S. 1998, The Netherlands: Kugler Publications, 241-246. Volume 1 1
Gold E: Serologic and virus-isolation studies of patients with varicella or herpes-zoster infection. New England J Med. 1966, 274 (4): 181-185. 10.1056/NEJM196601272740403.
Haanpaa M, Dastidar P, Weinberg A, Levin M, Miettenin A, Lapinlampi P, et al: CSF and MRI findings in patients with acute herpes zoster. Neurol. 1998, 51 (5): 1405-1411. 10.1212/WNL.51.5.1405.
Satyaprakash AK, Tremaine AM, Stelter AA, Arwen A, Creed R, Ravanfar P, et al: Viremia in acute herpes zoster. J Infect Dis. 2009, 20 (1): 26-32.
Brown H, Burns SK, Kaiser CN: The spinal accessory nerve plexus, the trapezius muscle, and shoulder stabilization after radical neck cancer surgery. Ann Surg. 1988, 208 (5): 654-661. 10.1097/00000658-198811000-00019.
Brown H: Anatomy of the spinal accessory nerve plexus: relevance to head and neck cancer and atherosclerosis. Exp Biol Med. 2002, 227 (8): 570-578.
Furuta Y, Ohtani F, Aizawa H, Fukuda S, Kawabata H, Bergström T: Varicella-zoster virus reactivation is an important cause of acute peripheral facial paralysis in children. Pediatr Infect Dis J. 2005, 24 (2): 97-101. 10.1097/01.inf.0000151032.16639.9c.
Aviel A, Marshak G: Ramsay hunt syndrome: a cranial polyneuropathy. Am J Otolaryngol. 1982, 3 (1): 61-66. 10.1016/S0196-0709(82)80035-5.
Jonsson L, Tien R, Engström M, Thuomas KA: Gd-DPTA enhanced MRI in Bell’s palsy and herpes zoster oticus: an overview and implications for future studies. Acta Otolaryngol. 1995, 115 (5): 577-584. 10.3109/00016489509139371.
Murakami S, Honda N, Mizobuchi M, Nakashiro Y, Hato N, Gyo K: Rapid diagnosis of varicella zoster virus infection in acute facial palsy. Neurol. 1998, 51 (4): 1202-1205. 10.1212/WNL.51.4.1202.
Yeo SW, Lee DH, Jun BC, Chang KH, Park YS: Analysis of prognostic factors in Bell’s palsy and Ramsay hunt syndrome. Auris Nasus Larynx. 2007, 34 (2): 159-164. 10.1016/j.anl.2006.09.005.
Agius AM, Pickles JM, Burch KL: A prospective study of otitis externa. Clin Otolaryngol Allied Sci. 1992, 17 (2): 150-154. 10.1111/j.1365-2273.1992.tb01063.x.
Love S, Coakham HB: Trigeminal neuralgia: pathology and pathogenesis. Brain. 2001, 124 (12): 2347-2360. 10.1093/brain/124.12.2347.
Dworkin RH, Johnson RW, Breuer J, Gnann JW, Levin MJ, Backonja M, et al: Recommendations for the management of herpes zoster. Clin Infect Dis. 2007, 44 (Suppl 1): 1-26.
Whitley RJ, Weiss H, Gnann JW, Tyring S, Mertz GJ, Pappas PG, et al: Acyclovir with and without prednisone for the treatment of herpes zoster. A randomized, placebo-controlled trial. Ann Intern Med. 1996, 125 (5): 376-383. 10.7326/0003-4819-125-5-199609010-00004.
Uscategui T, Doree C, Chamberlain IJ, Burton MJ: Corticosteroids as adjuvant to antiviral treatment in Ramsay hunt syndrome (herpes zoster oticus with facial palsy) in adults. Cochrane Database Syst Rev. 2008, 1-2. 3
Wood MJ, Johnson RW, McKendrick MW, Taylor J, Mandal BK, Crooks J: A randomized trial of acyclovir for 7 days or 21 days with and without prednisolone for treatment of acute herpes zoster. N Engl J Med. 1994, 330 (13): 896-900. 10.1056/NEJM199403313301304.
Uscategui T, Dorée C, Chamberlain IJ, Burton MJ: Antiviral therapy for Ramsay hunt syndrome (herpes zoster oticus with facial palsy) in adults. Cochrane Database Syst Rev. 2008, 1-2. 4
de Ru JA, van Benthem PP: Combination therapy is preferable for patients with Ramsay hunt syndrome. Otol Neurotol. 2011, 32 (5): 852-855. 10.1097/MAO.0b013e31821a00e5.
We thank the patient who agreed to have us write an article based on her experience. We also thank Nigel Worme for the design and creation of the cartoon images of Ramsay Hunt Syndrome. No funding bodies were involved.
The authors declare that they have no competing interest.
(MW) assessed the patient and decided to create a case report. She did a literature review, analyzed and interpreted the data, drafted and revised the manuscript. (RC) assessed and treated the patient in the family doctor’s office, acquired the data from the various clinics and emergency rooms and contributed to the manuscript drafting. (LL) did a literature review, analyzed and interpreted the data, contributed to drafting and revised the manuscript. All authors read and approved the final manuscript.
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Worme, M., Chada, R. & Lavallee, L. An unexpected case of Ramsay hunt syndrome: case report and literature review. BMC Res Notes 6, 337 (2013). https://doi.org/10.1186/1756-0500-6-337