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Volume 21, Number 11—November 2015

Neurologic Disorders in Immunocompetent Patients with Autochthonous Acute Hepatitis E

H. Blasco Perrin, P. Cintas, F. Abravanel, R. Gérolami, L. d'Alteroche, J.-N. Raynal, L. Alric, E. Dupuis, L. Prudhomme, E. Vaucher, P. Couzigou, J.-M. Liversain, C. Bureau, J.-P. Vinel, N. Kamar, J. Izopet, and J.-M. Peron
Author affiliations: Hôpital Purpan–CHU Toulouse, Toulouse, France (H. Blasco Perrin, P. Cintas, F. Abravanel, L. Alric, C. Bureau, J.-P. Vinel, J. Izopet, J.M. Peron); Hôpital de La Conception–CHU Marseille, Marseille, France (R. Gérolami); Hôpital Trousseau–CHU Tours, Tours, France (L. d'Alteroche); Clinique de l’Union, l’Union, France (J.-N. Raynal); Clinique Pasteur, Toulouse (E. Dupuis); CHIC Castres-Mazamet, Castres-Mazamet, France (L. Prudhomme); CH Narbonne, Narbonne, France (E. Vaucher); Hôpital du Haut-Lévêque–CHU Bordeaux, Bordeaux, France (P. Couzigou); CH Mont de Marsan, Mont de Marsan, France (J.-M. Liversain); Hôpital Ranguei–CHU Toulouse, Toulouse (L. Buscail, N. Kamar)

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Learning Objectives

Upon completion of this activity, participants will be able to:

•     Distinguish overall aspects of neurologic disorders occurring in immunocompetent patients infected with hepatitis E virus, based on a retrospective case series

•     Discuss mononeuritis multiplex occurring in immunocompetent patients infected with hepatitis E virus

•     Discuss Parsonage-Turner syndrome occurring in immunocompetent patients infected with hepatitis E virus.

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Disclosures: Hélène Blasco-Perrin, MD; Pascal Cintas, MD; Florence Abravanel, PharmD, PhD; René Gérolami, MD, PhD; Louis d'Alteroche, MD; Jean-Noël Raynal, MD; Emmanuel Dupuis, MD; Laurent Prudhomme, MD, PhD; Emmanuel Vaucher, MD; Patrice Couzigou, MD; Jean-Michel Liversain, MD; Louis Buscail, MD, PhD; Jean-Pierre Vinel, MD; Nassim Kamar, MD, PhD; Jacques Izopet, PharmD, PhD; and Jean-Marie Peron, MD, PhD, have disclosed no relevant financial relationships. Laurent Alric, MD, PhD, has disclosed the following relevant financial relationships: served as an advisor or consultant for MSD, BMS, Gilead; served as a speaker or a member of a speakers bureau for MSD; received grants for clinical research from Roche, Janssen, MSD, Gilead. Christophe Bureau, MD, PhD, has disclosed the following relevant financial relationships: served as an advisor or consultant for Norgine Inc.; served as a speaker or a member of a speakers bureau for W.L. Gore & Associates, Inc.; received grants for clinical research from W.L. Gore & Associates, Inc.



Neurologic disorders, mainly Guillain-Barré syndrome and Parsonage–Turner syndrome (PTS), have been described in patients with hepatitis E virus (HEV) infection in industrialized and developing countries. We report a wider range of neurologic disorders in nonimmunocompromised patients with acute HEV infection. Data from 15 French immunocompetent patients with acute HEV infection and neurologic disorders were retrospectively recorded from January 2006 through June 2013. The disorders could be divided into 4 main entities: mononeuritis multiplex, PTS, meningoradiculitis, and acute demyelinating neuropathy. HEV infection was treated with ribavirin in 3 patients (for PTS or mononeuritis multiplex). One patient was treated with corticosteroids (for mononeuropathy multiplex), and 5 others received intravenous immunoglobulin (for PTS, meningoradiculitis, Guillain-Barré syndrome, or Miller Fisher syndrome). We conclude that pleiotropic neurologic disorders are seen in HEV-infected immunocompetent patients. Patients with acute neurologic manifestations and aminotransferase abnormalities should be screened for HEV infection.

Hepatitis E virus (HEV) infection is an emerging autochthonous disease in industrialized countries (1). Locally acquired (autochthonous) HEV 3 or HEV 4 infections are believed to be a porcine zoonosis. The virus typically affects middle-aged or elderly men and can cause severe hepatitis, particularly in patients with an underlying liver disease (2). Chronic HEV infection occurs in recipients of a solid-organ transplant, in patients with hematologic malignancies, and in patients with HIV infection (3,4). Neurologic symptoms have been reported in up to 5% of patients with an HEV infection, indicating that HEV could have a specific neurotropism (5); most patients in this preliminary study were immunosuppressed. In developing countries, cases describing neurologic involvement during acute HEV infection have also been reported (6,7): most concerned Guillain-Barré syndrome (GBS) and Parsonage-Turner syndrome (PTS). Peripheral neuropathy, small-fiber neuropathy, and myositis have also been described (8,9). Peripheral nervous system tropism is not exclusive, and rare cases of myelitis and encephalitis have also been reported (10). Recently, studies of 2 national cohorts (in the United Kingdom and the Netherlands) have found that GBS and PTS were associated with acute HEV infection in 5% and 10% of cases, respectively (11,12). Here we describe an additional range of neurologic manifestations that were found during acute autochthonous HEV infection in immunocompetent patients.

Patients and Methods

This retrospective multicenter study was conducted in France from January 2006 through June 2013. All members of the French Liver Association (Association Française pour l’Etude du Foie, 500 members) were sent a newsletter inviting them to report cases of HEV infection in which neurologic symptoms were experienced. Data were recorded from patients with neurologic disorders, regardless of the symptoms exhibited during the course of acute HEV infection. This retrospective sampling was likely to capture most patients in France who had neurologic symptoms during acute HEV infection. A second newsletter was sent 6 months later to maximize the completeness of reporting. HEV infection was diagnosed by detecting anti-HEV IgM, HEV RNA, or both in serum or fecal samples from patients with elevated aminotransferase levels. All cases occurred in France, and all patients gave their informed consent.

The EIAgen (Adaltis, Eurobio, Bologna, Italy) and Wantai (Wantai Biologic Pharmacy Enterprise Co., Beijing, China) kits were used to detect antibodies (13). Both tests are highly specific and sensitive for detecting IgM against HEV. HEV RNA from serum, fecal samples, or cerebrospinal fluid (CSF) was detected by using a real-time PCR as described (3,14). All other causes of acute hepatitis were excluded, and patients had no co-infections. All patients were screened for other causes of disease with immunoassays (antinuclear antibodies, antipolynuclear neutrophil cytoplasmic antibodies) and underwent viral serologic testing (hepatitis B virus, hepatitis C virus, HIV, Epstein-Barr virus, cytomegalovirus). Campylobacter was also screened for. The cases of patients 5 and 12 have been reported (14).

Phylogenetic analyses were performed by sequencing a 347-nt fragment within the open reading frame 2 region as described (15). Nucleotide identity was analyzed with BioEdit software version (

Statistical Analyses

Data are presented as their medians (ranges) or their means (SDs). Student t-test was used to compare the quantitative variables. A p value <0.05 was considered significant.


Patient Characteristics and Clinical Outcomes

Fifteen patients (7 women, 8 men) from 7 different hospitals were included in this study. The clinical characteristics of the patients are reported in Table 1. The median age was 55 years (range 25–77 years). The median follow-up period was 42 weeks (range 4–161 weeks). All patients were immunocompetent. All but 1 lived in southern France: 11 lived in the southwest, 3 in the southeast, and 1 in central France.

No patient had underlying chronic liver disease; 2 patients had jaundice, 10 had asthenia, 5 had arthromyalgia, and 3 had fever. Three patients had neurologic symptoms only. Their biological characteristics are reported in Table 2. All patients had elevated liver enzyme levels, and none experienced liver failure. Median enzyme levels at diagnosis were the following: alanine aminotransferase level at diagnosis was 495 IU/L (range 49–3,641 IU/L; reference range 10–41 IU/l), aspartate aminotransferase 124 IU/L (range 37–1,742 IU/L; reference range 15–41 IU/l), bilirubin 15 µmol/L (range 4–101 µmol/L; reference range 3–21 µmol/l), alkaline phosphatase 254 IU/L (range 88–704 IU/L; reference range 36–126 IU/l), γ-glutamyl transferase 185 IU/L (range 33–783 IU/L; reference range 7-64 IU/l). Median prothrombin time was 96% (range 76%–100%).

All patients had IgM against HEV; 13 had IgG against HEV and 2 did not. Serum specimens of 14 patients underwent HEV PCR, and specimens from 11 patients were positive for HEV (Table 2). The median plasma HEV RNA concentration was 4.40 log-copies/mL (range 2.12–5.83).

We were able to sequence 7 virus strains from the patients: all belonged to genotype 3f, the main genotype identified in France. Phylogenetic analyses were conducted with these strains and HEV strains obtained by the French National Reference Center from patients who did not exhibit a neurologic disorder (Figure). The strains were scattered across the phylogenetic tree and were only 87.0%–93.5% identical.

Two patients had eaten game (wild boar and deer). All other patients had eaten pork. All patients had liver enzyme levels within the reference range at the last follow-up.

Neurologic Symptoms

Fourteen patients had been hospitalized. Neurologic symptoms were classified into 4 categories: mononeuritis multiplex, PTS, meningoradiculitis, and acute inflammatory demyelinating polyradiculoneuropathy (Table 3).

Mononeuritis Multiplex

Six patients (3 men and 3 women, patients 1–6) had mononeuritis multiplex; their median age was 54 years (range 25–77 years). Mononeuritis multiplex was defined by asymmetric, asynchronous involvement of the noncontiguous nerve trunks. All patients had experienced neuropathic pain and paresthesia in >1 nerve segments with hyporeflexia or areflexia. For 3 patiens, an electromyogram showed asymmetric axonal neuropathy, and various patterns of nerve involvement were observed. Patients 1 and 6 had confluent but asymmetric (>50%) lower-limb neuropathy (musculocutaneous and external saphenous). Patients 3 and 4 had multiple radicular or proximal troncular neuropathies, and patient 5 had troncular median and internal brachial cutaneous-nerve involvement. Three patients had asthenia and 1 had jaundice; HEV RNA was detected by PCR in serum samples from 4 patients (patients 1, 2, 5, 6).

One patient (patient 6) received specific antiviral treatment. He was given ribavirin, initially at a dose of 400 mg for 7 days (5.5 mg/kg/d) and was then given 600 mg/day (8.5 mg/kg/d) for 3 months. A serum specimen was negative for HEV after 10 days of treatment. Patient 3 was given corticosteroids for 10 weeks. Five patients had no sequelae at the last follow-up (median 33 weeks [range 4–157 weeks]). One patient (patient 2), at the last follow-up at 4 weeks, had ongoing paresthesia in a nerve segment in the lower limbs.


Four patients (3 men and 1 woman, patients 7–10) exhibited PTS, also known as neuralgic amyotrophy. Their median age was 55.5 years (range 51–56 years). These patients sought treatment at the hospital for asthenia and acute neuropathic pain in the shoulder. PTS was bilateral but asymmetric in 3 patients. Asymmetric paresis and amyotrophia appeared within a few days, with the concomitant decrease in pain. Tendon reflexes were reduced or eliminated in 2 patients (patients 9 and 10). For 3 patients, an electromyogram confirmed bilateral patchy denervation, predominantly of the upper trunk of the brachial plexus. For 2 patients (patients 7 and 10), analysis of CSF showed high levels of proteins, levels of cells in reference ranges, and glucose level within reference range. HEV PCR of a CSF specimen was not done.

HEV was diagnosed after IgM against HEV was detected in 1 patient (patient 9) and after HEV RNA was detected in the serum of 3 patients (patients 7, 8, 10). Patients 7 and 10 were given ribavirin (for, respectively, 3 weeks and 2 months) at a dose of 800 mg/day. This treatment was well tolerated. They also received intravenous immunoglobulin (IVIg) at a dose of 25 g/day (patient 7) or 35 g/day (patient 10) for 5 days. All patients but 1 had persistent weakness at the last follow-up (median 71 weeks [range 16–126 weeks]); none had received a control electromyogram. Assessment of patients through disability scales was not possible because this study was retrospective and involved many centers. Notably, the only asymptomatic patient at follow-up was the patient that received both ribavirin and IVIg.


Three patients (2 women and 1 man, patients 11–13) had meningoradiculitis. They were, respectively, 74, 54, and 33 years of age. These patients sought treatment for meningitis symptoms (headache, photophobia) and radiculitis with pain and paresthesia restricted to 1 or a few radicular topographies. CSF was clear and showed lymphocytic meningitis with >90% lymphocytes, a high level of protein (0.79–1.37 g/L, reference range 0.28–0.53 g/L), and glucose levels within reference ranges. Patient 11 had jaundice. PCR of all serum samples from all patients with meningoradiculitis showed HEV RNA. For 2 patients, PCR of CSF was positive for HEV (patients 11 and 12). One woman was breast feeding (patient 13); HEV was detected in her serum but not in breast milk. PCR detected HEV in fecal samples from 2 patients (patients 11 and 13). Patient 11 was treated with IVIg at 0.5 g/kg/day for 4 days. No patient was symptomatic at the last follow-up visit. The median time to follow-up was 119 weeks (range 77–161 weeks).

Acute Inflammatory Demyelinating Polyradiculoneuropathy

Two patients exhibited acute inflammatory demyelinating polyradiculoneuropathy: 1 had GBS, and 1 had Miller-Fisher syndrome. Patient 14, a 60-year-old woman, was hospitalized for GBS. Initially, she had asthenia and acute low back pain. She had a positive viral load for HEV IgG and IgM. A neurologic examination revealed generalized areflexia and weakness in the lower limbs. GBS was confirmed in nerve-conduction studies. She had no hepatic symptoms. CSF analysis showed a high level of protein (2 g/L, reference range 0.28–0.53 g/L) and no HEV RNA. She was treated with IVIg for 5 days at a dose of 400 mg/day, and the symptoms partially regressed. By 5 weeks later, weakness of the lower limbs had improved, but she still experienced persistent areflexia.

Patient 15, a 54-year-old man, was hospitalized for weight loss. A neurologic examination revealed quadridistal hypoesthesia with ataxia, areflexia, and diplopia due to paresia of the right VI nerve. CSF protein concentration was elevated (1.46 g/L, reference range 0.28–0.53 g/L), and albumino-cytologic dissociation was found. Nerve-conduction studies confirmed demyelinating neuropathy. These findings were conclusive for Miller-Fisher syndrome. He had no hepatic symptoms. Serum was positive for IgM against HEV. Serum and fecal samples were negative for HEV by PCR. He received IVIg for 5 days at a dosage of 2 g/kg and was hospitalized for 1 week. His neurologic symptoms improved but did not totally disappear until >13 weeks of follow-up (persistent ataxia).


This study shows the wide spectrum of neurologic injuries associated with patients with an acute HEV autochthonous infection. Because the study was retrospective, it was not possible to identify the prevalence of HEV infection in patients with neurologic symptoms or the prevalence of neurologic symptoms in patients with HEV infection.

Neurologic symptoms could be divided into 4 entities. Notably, the first dominant finding was mononeuritis multiplex, observed in 6 of the 15 patients, with asymmetric, asynchronous, and painful segmental nerve involvement. This condition was also the main entity in the original report, which also included immunocompromised patients with chronic HEV-3 infection (5). In previous reports in immunocompetent patients, painful peripheral neuropathy has rarely been reported (8). However, mononeuritis multiplex is a common complication in immune and viral diseases. A vasculitis process can be hypothesized, but none of the patients in this study underwent a nerve biopsy. Additional investigations, including anatomopathologic exploration, would be needed to further explore the physiopathologic (antiviral and/or immunosuppressive) pathways.

The next most frequent manifestation was PTS, also called brachial neuritis or neuralgic amyotrophy, which was found in 4 patients. PTS is a rare pathologic condition, defined by sudden, acute, and unbearable pain across the top of the shoulder, followed by severe amyotrophy. As was exhibited by the patients described here, PTS can be unilateral or bilateral but is asymmetric. A recent study reported cases of acute HEV infection in a cohort of 47 patients from Cornwall (UK) and the Netherlands (12); 5 cases (10.6%) of acute HEV infection were identified, indicating that HEV may be a major cause of PTS in industrialized countries with a high prevalence of HEV. That study also suggested that HEV-associated brachial neuritis more commonly produces bilateral symptoms and signs than brachial neuritis produced by other causes. In our study, 3 of 4 patients had bilateral symptoms. Three of the 4 patients with PTS had neurologic sequelae at the last follow-up (71 weeks), which suggests that concomitant HEV infection may represent a poor prognostic factor. Van Eijk et al. (12) found that all 5 of their HEV-positive patients exhibited persistent weakness at 6 months.

There is no specific treatment identified for PTS, but it is known to be immune mediated. However, we cannot exclude direct infection of the brachial plexus. Three of the 4 patients in our study had serum samples positive for HEV by PCR, indicating active replication. Two patients were treated with ribavirin as an antiviral therapy. This antiviral therapy is recommended to treat chronic hepatitis E in organ-transplant recipients (16,17). Case reports on the treatment of acute HEV infection in immunocompetent patients have been published, with promising results (1821). We found that the only patient who had no persisting symptoms at the last follow-up had been treated with a combination of ribavirin and IVIg.

The third neurologic entity we found was meningoradiculitis in 3 patients. HEV was detected in the CSF of 1 case-patient, indicating neurotropism and the direct effect of HEV. This condition is probably the only one in which HEV may be directly responsible for the neurologic manifestations. No neurologic sequelae were seen in this group. A previous study found quasispecies compartmentalization in an immunocompromised patient with neurologic manifestations, and its temporal association suggests that neurologic symptoms could be linked to the emergence of neurotropic variants (22). The factors associated with HEV neurotropism need to be investigated further.

The last entity was acute inflammatory demyelinating polyradiculoneuropathy, which was seen in 2 patients. This condition can be classically triggered by many viruses, including hepatotropic viruses (23). An immune response that cross-reacts with axonemal or Schwann cell antigens is elicited and results in damage to the peripheral nerves. Both patients had persisting neurologic symptoms, commonly seen in this disease (11). Although several studies have demonstrated that HEV infection can induce GBS, this condition was found in only 2 of our patients. In a cohort of GBS case-patients from Bangladesh, seroprevalence of IgM against HEV was 11%, compared with 2% in a control group of patients with other neurologic disease (7). The frequency of HEV infection was recently determined in a cohort of 201 patients with GBS in the Netherlands and was found to have occurred in 5% (11).

The number of patients in this study is too small to draw definitive conclusions on the sex ratio for these conditions, but the ratio was highest in the PTS group. We also found that neurologic disorders occurred only in those with a HEV 3f genotype, although this is the most common genotype in France (24), so other HEV subtypes and genotypes may induce neurologic symptoms (5). Moreover, because only patients with elevated liver enzyme levels were included, neurologic complications were probably underestimated in this study, in particular, for GBS and PTS, for which conditions the neurologic symptoms are often delayed after the initial event is triggered.

Patients with PTS had significantly higher values in liver enzyme tests (aspartate aminotransferase, γ-glutamyl transpeptidase) than patients with mononeuritis multiplex. We have no definitive explanation, but this finding could be due to the earlier appearance of PTS symptoms during the course of HEV infection.

Three patients were treated with ribavirin with the aim of shortening the disease’s duration: the 2 PTS patients and 1 patient with mononeuritis multiplex. One needed blood transfusions and erythropoietin. Whether ribavirin shortened the evolution of neurologic symptoms, particularly for patients with PTS, needs to be studied further.

One limitation of our study is the retrospective sampling by emailing through the French Liver Association. Although this method provides the advantage of reaching most practitioners who diagnose HEV infection throughout France, it may have induced an ascertainment bias, that is, the true frequency of the neurologic symptoms during HEV infection is difficult to assess. In addition, patients with neurologic symptoms who were not referred to a hepatologist obviously were not accounted for.

In summary, HEV-3 infection can induce a wide range of neurologic symptoms, including mononeuritis multiplex, PTS, meningoradiculitis, and inflammatory demyelinating polyradiculoneuropathy. Sequelae were seen with mononeuropathy multiplex, PTS, and inflammatory demyelinating polyradiculoneuropathy. Only 2 patients had overt hepatitis with jaundice. Therefore, we recommend screening patients with elevated liver enzyme levels and neurologic symptoms for HEV infection, regardless of other symptoms. Treatment with ribavirin needs to be assessed further.

Dr. Blasco-Perrin was an intern from 2010 to 2015 at the Toulouse University hospital in the gastrointestinal and hepatology units. She will be a fellow in the hepatology unit, Purpan Hospital, CHU Toulouse, France, in 2016. Her research interests focus on viral hepatitis, in particular, hepatitis E.



  1. Kamar  N, Bendall  R, Legrand-Abravanel  F, Xia  NS, Ijaz  S, Izopet  J, Hepatitis E. Lancet. 2012;379:247788 . DOIPubMedGoogle Scholar
  2. Péron  JM, Bureau  C, Poirson  H, Mansuy  JM, Alric  L, Selves  J, Fulminant liver failure from acute autochthonous hepatitis E in France: description of seven patients with acute hepatitis E and encephalopathy. J Viral Hepat. 2007;14:298303. DOIPubMedGoogle Scholar
  3. Kamar  N, Selves  J, Mansuy  JM, Ouezzani  L, Peron  JM, Guitard  J, Hepatitis E virus and chronic hepatitis in organ-transplant recipients. N Engl J Med. 2008;358:8117. DOIPubMedGoogle Scholar
  4. Tavitian  S, Peron  JM, Huynh  A, Mansuy  JM, Ysebaert  L, Huguet  F, Hepatitis E virus excretion can be prolonged in patients with hematological malignancies. J Clin Virol. 2010;49:1414. DOIPubMedGoogle Scholar
  5. Kamar  N, Bendall  RP, Peron  JM, Cintas  P, Prudhomme  L, Mansuy  JM, Hepatitis E virus and neurologic disorders. Emerg Infect Dis. 2011;17:1739. DOIPubMedGoogle Scholar
  6. Cheung  MC, Maguire  J, Carey  I, Wendon  J, Agarwal  K. Review of the neurological manifestations of hepatitis E infection. Ann Hepatol. 2012;11:61822 .PubMedGoogle Scholar
  7. GeurtsvanKessel CH. Islam Z, Mohammad QD, Jacobs BC, Endtz HP, Osterhaus AD. Hepatitis E and Guillain-Barré syndrome. Clin Infect Dis. 2013;57:136970.PubMedGoogle Scholar
  8. Woolson  KL, Forbes  A, Vine  L, Beynon  L, McElhinney  L, Panayi  V, Extra-hepatic manifestations of autochthonous hepatitis E infection. Aliment Pharmacol Ther. 2014;40:128291. DOIPubMedGoogle Scholar
  9. Del Bello  A, Arne-Bes  MC, Lavayssiere  L, Kamar  N. Hepatitis E virus-induced severe myositis. J Hepatol. 2012;57:11523. DOIPubMedGoogle Scholar
  10. Deroux  A, Brion  JP, Hyerle  L, Belbezier  A, Vaillant  M, Mosnier  E, Association between hepatitis E and neurological disorders: two case studies and literature review. J Clin Virol. 2014;60:602. DOIPubMedGoogle Scholar
  11. Van den Berg  B, van der Eijk  AA, Pas  SD, Hunter  JG, Madden  RG, Tio-Gillen  AP, Guillain-Barré syndrome associated with preceding hepatitis E virus infection. Neurology. 2014;82:4917. DOIPubMedGoogle Scholar
  12. Van Eijk  JJ, Madden  RG, van der Eijk  AA, Hunter  JG, Reimerink  JH, Bendall  RP, Neuralgic amyotrophy and hepatitis E virus infection. Neurology. 2014;82:498503. DOIPubMedGoogle Scholar
  13. Abravanel  F, Chapuy-Regaud  S, Lhomme  S, Miedouge  M, Peron  JM, Alric  L, Performance of anti-HEV assays for diagnosing acute hepatitis E in immunocompromised patients. J Clin Virol. 2013;58:6248. DOIPubMedGoogle Scholar
  14. Despierres  LA, Kaphan  E, Attarian  S, Cohen-Bacrie  S, Pelletier  J, Pouget  J, Neurologic disorders and hepatitis E, France, 2010. Emerg Infect Dis. 2011;17:15102 .PubMedGoogle Scholar
  15. Legrand-Abravanel  F, Mansuy  JM, Dubois  M, Kamar  N, Peron  JM, Rostaing  L, Hepatitis E virus genotype 3 diversity, France. Emerg Infect Dis. 2009;15:1104. DOIPubMedGoogle Scholar
  16. Mallet  V, Nicand  E, Sultanik  P, Chakvetadze  C, Tesse  S, Thervet  E, Brief communication: case reports of ribavirin treatment for chronic hepatitis E. Ann Intern Med. 2010;153:859 and. DOIPubMedGoogle Scholar
  17. Kamar  N, Rostaing  L, Abravanel  F, Garrouste  C, Lhomme  S, Esposito  L, Ribavirin therapy inhibits viral replication on patients with chronic hepatitis e virus infection. Gastroenterology. 2010;139:16128. DOIPubMedGoogle Scholar
  18. Péron  JM, Dalton  H, Izopet  J, Kamar  N. Acute autochthonous hepatitis E in western patients with underlying chronic liver disease: a role for ribavirin? J Hepatol. 2011;54:13234, author reply 4–5 . DOIPubMedGoogle Scholar
  19. Pischke  S, Hardtke  S, Bode  U, Birkner  S, Chatzikyrkou  C, Kauffmann  W, Ribavirin treatment of acute and chronic hepatitis E: a single-centre experience. Liver Int. 2013;33:7226 .DOIPubMedGoogle Scholar
  20. Goyal  R, Kumar  A, Panda  SK, Paul  SB, Acharya  SK. Ribavirin therapy for hepatitis E virus–induced acute on chronic liver failure: a preliminary report. Antivir Ther. 2012;17:10916. DOIPubMedGoogle Scholar
  21. Gerolami  R, Borentain  P, Raissouni  F, Motte  A, Solas  C, Colson  P. Treatment of severe acute hepatitis E by ribavirin. J Clin Virol. 2011;52:602. DOIPubMedGoogle Scholar
  22. Kamar  N, Izopet  J, Cintas  P, Garrouste  C, Uro-Coste  E, Cointault  O, Hepatitis E virus–induced neurological symptoms in a kidney-transplant patient with chronic hepatitis. Am J Transplant. 2010;10:13214. DOIPubMedGoogle Scholar
  23. Hughes  RACH, Cornblath  DR. Guillain-Barré syndrome. Lancet. 2005;366:165366. DOIPubMedGoogle Scholar
  24. Mansuy  JM, Abravanel  F, Miedouge  M, Mengelle  C, Merviel  C, Dubois  M, Acute hepatitis E in south-west France over a 5-year period. J Clin Virol. 2009;44:747 . DOIPubMedGoogle Scholar




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Article Title: Neurologic Disorders in Immunocompetent Patients with Autochthonous Acute Hepatitis E

CME Questions

1. Your patient is a 52-year-old man with an acute onset of severe shoulder pain and weakness and moderate elevation in transaminase levels. According to the retrospective case series by Blasco-Perrin and colleagues, which of the following statements about the overall aspects of neurologic disorders occurring in immunocompetent patients infected with hepatitis E virus (HEV) is correct?

A.        The 4 syndromes reported were mononeuritis multiplex, Parsonage-Turner syndrome (PTS), ischemic stroke, and hemorrhagic stroke

B.        Ten of the 15 patients had overt hepatitis with jaundice

C.        All of the patients had complete, spontaneous resolution of their neurologic symptoms without HEV treatment

D.        Patients with acute neurologic manifestations and abnormalities in transaminase levels should be screened for HEV

2. According to the retrospective case series by Blasco-Perrin and colleagues, which of the following statements about mononeuritis multiplex occurring in immunocompetent patients infected with HEV is correct?

A.        Two of the 15 patients had mononeuritis multiplex

B.        This condition is characterized by asymmetric, asynchronous, and painful segmental-nerve involvement

C.        Nerve biopsy result proved that this was a vasculitic process

D.        All of the patients had neurologic sequelae at last follow-up

3. According to the retrospective case series by Blasco-Perrin and colleagues, which of the following statements about PTS occurring in immunocompetent patients infected with HEV is correct?

A.        PTS, also called brachial neuritis or neuralgic amyotrophy, occurred in 4 of the 15 patients

B.        PTS is a common condition associated with sudden, acute, severe elbow pain followed by severe amyotrophy

C.        All of the patients with PTS had neurologic resolution by the last follow-up

D.        This condition is known to be caused only by direct HEV infection of the affected nerve(s)

Activity Evaluation

1. The activity supported the learning objectives.

Strongly Disagree

Strongly Agree






2. The material was organized clearly for learning to occur.

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Strongly Agree






3. The content learned from this activity will impact my practice.

Strongly Disagree

Strongly Agree






4. The activity was presented objectively and free of commercial bias.

Strongly Disagree

Strongly Agree







Cite This Article

DOI: 10.3201/eid2111.141789

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Table of Contents – Volume 21, Number 11—November 2015

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Page created: October 19, 2015
Page updated: October 19, 2015
Page reviewed: October 19, 2015
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.