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The European Register of Cystic Echinococcosis, ERCE: state-of-the-art five years after its launch



The real burden of human cystic echinococcosis (CE) remains elusive, due to the peculiar characteristics of the disease and the heterogeneous and incomplete data recording of clinical cases. Furthermore, official notification systems do not collect pivotal clinical information, which would allow the comparison of different treatment outcomes, and thus circumvent the difficulty of implementing clinical trials for CE. The Italian Register of CE (RIEC) was launched in 2012 and expanded in 2014 into the European Register of CE (ERCE). The primary aim of the ERCE was to highlight the magnitude of CE underreporting, through the recording of cases that were not captured by official records. We present an overview of data collated in the ERCE and discuss its future, five years after its inception.


The ERCE database was explored on March 31st 2019; data concerning participating centres and registered cases were descriptively analysed.


Forty-four centres from 15 countries (7 non-European) were affiliated to the ERCE. Thirty-four centres (77%) registered at least one patient; of these, 18 (53%) recorded at least one visit within the past 18 months. A total of 2097 patients were registered, 19.9% of whom were immigrants. Cyst characteristics were reported for at least one cyst at least in one visit in 1643 (78.3%) patients, and cyst staging was used by 27 centres. In total, 3386 cysts were recorded at first registration; mostly located in the liver (75.5%). Data concerning clinical management could be analysed for 920 “cyst stage-location-management” observations, showing great heterogeneity in the implementation of the stage-specific management approach recommended by the WHO.


The ERCE achieved its goal in showing that CE is a relevant but neglected public health problem in Europe and beyond, since a proportion of patients reaching medical attention are not captured by official notification systems. The ERCE may provide a valuable starting platform to complement hospital-derived data, to obtain a better picture of the epidemiology of clinical CE, and to collect clinical data for the issue of evidence-based recommendations. The ERCE will be expanded into the International Register of CE (IRCE) and restructured aiming to overcome its current criticalities and fulfil these aims.


Cystic echinococcosis (CE) is a parasitic zoonosis, listed among the neglected diseases for which the World Health Organization (WHO) advocates concentrated control efforts [1]. Human CE is caused by the tapeworm Echinococcus granulosus (sensu lato) species complex, naturally transmitted between canids (mainly the domestic dog) and ungulates (mainly livestock, especially sheep) in a faecal-oral and predator-prey cycle. After the accidental ingestion of infective eggs by humans, the parasite develops as fluid-filled cysts (metacestodes) in organs and tissues, mainly the liver and lungs [2]. CE is mostly endemic in rural areas of China, Central Asia, South America, the Mediterranean, East Africa, and Australia, where livestock breeding is practiced [3].

Current CE burden estimates indicate globally about 300,000 disability adjusted life years, and an annual cost of about 200 million USD for human treatment of CE [4]. However, these estimates, based on highly heterogeneous and incomplete data sources, are largely underestimated, resulting in misperception of the magnitude of CE public health impact. Figures actually triplicate when accounting for estimated underreporting of cases reaching medical attention, not taking into consideration the disease burden carried by infected people not accessing health care [4]. Underreporting at national and supra-national level (e.g. to the European Centre for Diseases Prevention and Control, ECDC) derives from many factors. In Europe, CE notification requirements vary and are applied differently from country to country [5]. Further, the origin and type of available official data is heterogeneous (case-based or aggregated, from laboratories or hospitals or physicians), derived mainly from hospitalization records [5,6,7,8]. Patients managed as outpatients are largely not captured by official statistics, and notification of hospital cases to a central level is often incomplete. Moreover, in official European records, species differentiation between E. granulosus (s.l.) and Echinococcus multilocularis, the agent of alveolar echinococcosis (AE), is limited, adding to the inaccuracy of data [9, 10].

Official data are collected at national and supra-national level for epidemiological purposes. Pivotal data characterizing the course and clinical decision making for the management of this complex infection, such as cyst stage, clinical management details, and outcomes, are not collected. CE is a chronic, generally low-prevalence disease with heterogeneous clinical manifestations (including cyst number, location, size, stage, symptoms, complications and so on) that develops over years and requires a very long follow-up period to ascertain the outcome of the chosen clinical management approach [11,12,13]. Consequently, prospective clinical trials are virtually impossible to perform and treatment recommendations are largely based on expert opinion, which are, in turn, not widely followed [14, 15]. This often results in the administration of inappropriate treatments, which burden both patients and health care systems [16, 17].

In 2012, the WHO Collaborating Centre for Clinical Management of Cystic Echinococcosis (San Matteo Hospital Foundation, University of Pavia, Italy) and the Italian National Health Institute (Istituto Superiore di Sanità, Rome, Italy), through funding from the Sardinian Experimental Zooprophylactic Institute (Sassari, Italy), launched the Italian Register of Cystic Echinococcosis (RIEC) [18]. This aimed to respond to a long-standing need for an accessible register of CE cases, built to consider the peculiar characteristics of this infection. In 2014, RIEC was restructured and expanded into the European Register of Cystic Echinococcosis (ERCE), in the context of the European FP7 project “HERACLES” [19]. The main aims of the register were: (i) to indicate the magnitude of the problem represented by CE (mainly by recording cases otherwise not captured by official records, such as those only managed as outpatients); (ii) to bring the importance of CE to the attention of health authorities; (iii) to encourage public health policies for its control; and (iv) to support epidemiological, biological, and clinical research on CE by establishing a prospective case retrieval through the collection of data in a harmonized manner. Moreover, the ERCE supports the biobank repository of biological material derived from patients with CE and E. granulosus (s.l.) parasites (EchinoBioBank), established in Salamanca, Spain, in the context of the HERACLES project.

The structure and requirements of the ERCE are shown in Table 1 and have been described in detail in a previous publication on the first meeting of the ERCE network that took place in Rome in 2015 [19]. Here, we present an overview of data present in the ERCE and discuss its future development, five years after its launch.

Table 1 Schematic overview of the structure and features of the ERCE


The complete ERCE database explored on March 31st 2019. Analysed data referred to participating centres (number, country, date of joining the ERCE network, centre’s activity identified as recording of visits in the previous 18 months, total recorded cases and follow-up visits), and registered cases (sex, age, country of birth, cysts characteristics and clinical management at each visit). For the analysis of clinical management, only the data of patients whose records included cyst stage, location, and clear indication of management at defined visits, occurring after the date of first recording in ERCE, were extrapolated from the database. The descriptive analysis of the stage-specific management of CE was carried out as if each observation of the set “cyst stage-location-management” was an independent observation. That is, an individual cyst in a given localization in a patient, which was observed N times in different cyst stage and/or assigned to a different clinical management option, was analysed here as “N observations”. Only when a change in cyst stage and/or management allocation was recorded, a new observation was scored. Data were summarized as counts and percentages.


On March 31st 2019, 44 centres from 15 countries (Fig. 1), seven of which are non-European, were affiliated to ERCE. Centres joining the ERCE steadily increased over the years (Fig. 2). Of the affiliated centres, 34 (77%) registered at least one patient and, of these, 18 (53%) recorded at least one visit within the past 18 months (Figs. 1, 2). The absence of data from those centres that never entered patients’ information in the database (Fig. 2) is most likely due to a variable combination of reasons. These include absence of new diagnoses of CE or follow-up visits of patients managed in the centre (especially in hospitals that are not referral centres for CE or that joined the register only very recently), duties overload or change of position of the clinician who originally joined voluntarily the network.

Fig. 1

Countries and number of centres involved in the ERCE. Only the centres that registered at least one patient are included

Fig. 2

Affiliation and current activity of the ERCE network centres. Bars represent the cumulative number of affiliated centres at each year of activity of the RIEC (2012–2013) and ERCE (2014 onwards). Current activity status of affiliated centres is shown in the 2019 bar. Light grey indicates centres that never entered patients’ information in the database; white indicates 3 centres in France that send their data to a National reference centre which entered these patients’ information in the database; dark grey indicates centres that entered at least 1 patients’ information in the database since their affiliation but did not enter new data in the past 18 months; black indicates centres that entered new patients’ information in the database in the past 18 months

A total of 2097 patients were registered at the date of data extraction; of these, 831 (40%) were registered in 16 Italian centres (Fig. 3). Notably, a total of 119 patients (5.7% of all patients registered in ERCE) were detected during the ultrasound-based population screening carried out in 2014–2015 in Bulgaria, Romania and Turkey, in the context of the HERACLES project [20]. These patients are 12.2% of those registered in Sofia (Bulgaria), 9.6% of those registered in Bucharest (Romania), and 45.3% of those registered in Ankara (Turkey). The distribution of patients by sex and age at first registration in the ERCE is shown in Fig. 4; 53.1% of patients were females and 46.9% males, showing this even distribution between sexes throughout all age groups, most patients (66.4%) were in the adult 30–69 years age group (mean age 46.20 years, range 2–97 years). Additional file 1: Table S1 shows the country of birth of registered patients. Immigrants (defined as patients with CE who were born in a country different to that of enrolment), constituted 19.9% of the total registered patients; however, their relative percentage by centre, unsurprisingly, varied greatly among centres.

Fig. 3

Number of patients in the ERCE by country of registration

Fig. 4

Age groups and sex of patients registered in the ERCE

Echinococcal cyst characteristics (organ involved and/or cyst stage) were reported by 28 centres (representing 82.4% of centres having registered at least one patient) at least in one visit for at least one cyst in 1643 (78.3%) of patients. Although cyst staging according to the WHO-IWGE (Informal Working Group on Echinococcosis) classification [14] was used by 27 centres (i.e. 79.4% of centres having registered at least one patient); however, cyst stage, when applicable, was not constantly reported in all patients registered in individual centres and/or at each visit of the same patient. At first registration, for example, cyst staging was not reported for one-third of registered cysts (Table 2).

Table 2 Cyst characteristics at first registration in the ERCE (for the subset of patients for whom these data were recorded by the data entering clinician)

At first registration in ERCE, the majority (n = 1162/1966; 59.1%) of patients who had information on cyst number recorded had a single cyst; 153 (7.8%) had no cysts and were registered as patients with only post-surgical cavities/scars (Table 2). In total, 3409 cysts were recorded at first registration; the most frequent localization was the liver (n = 2557 cysts; 75.5%), followed by the lungs (n = 597 cysts; 17.5%) (Table 2). Other localizations, accounting for 7.5% of recorded cysts, included abdominal cavity, bone, central nervous system, heart, kidneys, muscle, pancreas, pelvis, skin and subcutaneous tissue, and spleen; 78 (3.9%) patients had cysts in more than one organ. Table 2 also summarizes the distribution of cyst stages recorded at first registration, classified according to the WHO-IWGE classification [14].

Treatments carried out prior to ERCE registration, as well as clinical management upon registration and subsequent follow-up visits, are also recorded in the register. Seventeen centres (representing 50.0% of centres having registered at least one patient) recorded at least once one follow-up visit for at least one patient; in these centres, 435 patients had at least one follow-up visit recorded (a median of 21% patients per centre, ranging from 1.6% to 84.2%). Data concerning the clinical management of patients could be analysed for 523 patients registered in 24 centres, for 726 cysts. As 82 patients had at least one follow-up visit recorded in which a change in cyst stage and/or management allocation was indicated, the total number of “cyst stage-location-management” observations analysed was 920 (Additional file 1: Table S2). A stage-specific approach is recommended by the WHO-IWGE for asymptomatic CE cysts of the liver. We analysed the data concerning the clinical approach of hepatic cysts according to cyst stage. Results are summarized in Table 3. These results need to be evaluated while acknowledging the fact that no information is recoded in the ERCE register concerning symptoms or other clinical factors that may induce the treating physician to deviate from the recommended stage-specific approach. The clinical management used for cysts in other organs is summarized in Additional file 1: Table S2. One centre from a non-European country, systematically did not indicate any cyst stage and all cases were managed surgically, with no indication of associated albendazole prophylaxis in the virtual totality of cases.

Table 3 Clinical management approach of hepatic CE cysts by stage


The primary aim of the ERCE, at its launch, was prominently of a public health perspective, to indicate to stakeholders the magnitude of the problem represented by CE and its underreporting, through the recording of cases not captured by official records [19]. Since its launch, new centres are joining the ERCE over time, demonstrating that CE, although neglected, is of interest for clinicians diagnosing and managing patients with CE, in European and non-European countries alike. In the time between data analysis and the writing of this paper, a 45th centre, in Afghanistan, joined the ERCE. This is of particular interest because no epidemiological data on CE are available in this country, published data being limited to case reports of patients from Afghanistan diagnosed in other countries [3]. In our cohort described here, 39 patients from Afghanistan were recorded in Iran and Austria ERCE-affiliated centres (Additional file 1: Table S1). Data collected in the ERCE, therefore, could highlight the neglected status of CE in endemic countries and constitute an important starting point to tackle this problem.

Since joining the register and recording of patients is voluntary and relies entirely on the time and goodwill of single clinicians, it is difficult to compare the figures recorded in the ERCE with those of official records. However, data collected in the ERCE show that a proportion of patients reaching medical attention are indeed managed with approaches not requiring hospitalization, and are therefore largely not captured by those notification systems which are based only on hospital discharge records [21]. We found, unsurprisingly, that a variable proportion of patients originate from countries different from the country of registration, both within and outside Europe. The increase of the migration phenomenon at global level [22] seems to cause an increase in CE cases seen in non-endemic areas [23] as well as an additional burden in CE-endemic countries. The ERCE could be, therefore, a useful tool to complement hospital-derived data, to obtain a better picture of the epidemiological situation of clinical CE and support public health analyses and planning of targeted interventions. Furthermore, the ERCE aims to capture only probable or confirmed CE cases, based on the current definition of the WHO-IWGE [14], with diagnosis based on the visualization on imaging of a lesion with features compatible with or pathognomonic of CE. This is different from the case definition of “echinococcosis” adopted at national and supra-national level in Europe, as currently official data not only do not distinguish between cases of CE and AE, but also allow patients positive solely on serology but with no evidence of actual cysts, to be recorded as “confirmed echinococcosis” cases [10].

In contrast to official data reports, the ERCE has been structured to collect prospectively and in a harmonized manner several clinical features of CE cases over follow-up visits. CE is a generally low-prevalence, chronic infection with extremely variable clinical presentations; it cannot be managed using a “one-fits-all” approach, and years-long follow-up is required to ascertain the outcome of any clinical management approach. As a result, prospective clinical trials are extremely difficult to conduct. The WHO-IWGE encouraged the clinical community to join shared data platforms to collect prospectively and analyse highly standardized clinical data as, in such a situation, it is possible to obtain valid comparisons of different treatments using data from observational studies, provided specific prerequisites are fulfilled [24]. The ERCE can thus be a valuable template from which further tailoring a tool fulfilling these prerequisites, to accomplish this ambitious goal.

At the time of the present analysis, it was possible to evaluate the matching cyst characteristics-management option only for about 25% of patients. On the one hand, this highlights the problem of suboptimal data completeness and quality, which derives from the voluntary nature of adherence to and feeding data into the register. On the other hand, this result may also have its roots in the scarce knowledge and application of the CE cyst staging system and the stage-specific clinical management approach recommended by the WHO-IWGE [13, 14]. This is exemplified by the case of one centre in a non-European country, where, systematically, no cyst stage was ever indicated, and all cases were reported to have been managed surgically. Although many variables, other than cyst stage, that may influence a physician to choose a treatment option, are not currently captured in the ERCE, where cyst staging is being used at least some stage-specific approaches seem to be applied. For example, the “watch and wait” approach was reported for over 80% of the observations concerning hepatic inactive (CE4-CE5) cysts. It is plausible to deduce that knowledge of cyst staging and applying the stage-specific approach are mutually related.

The ERCE, as it stands, suffers from several critical issues, especially regarding data quality and completeness, which will be addressed in the future, to fulfil the aims envisioned above. As mentioned, the voluntary nature of joining the register, and the reliance on the motivation of single clinicians to enter data for a period of long time, condition the variable quality of the entered data. However, additional informatics tools may be introduced to foster the accuracy and completeness of data entered, such as automatic crosschecking of data for incongruences. In addition, the option to upload cyst images should be implemented, to validate data before comparisons of different treatments is attempted. Finally, other prognostic factors relevant to treatment outcomes must be included, to allow drawing evidences from such case series.


To conclude, the ERCE achieved its goal in showing that CE is a neglected but relevant public health problem in Europe and beyond, as indicated by the data collected so far and by the growing interest shown by European and non-European clinicians. Current data collected in the ERCE highlight the need for the development and implementation of a better notification system, at least at the European level, without which a realistic picture of the prevalence and burden of human CE cannot be achieved. In addition, the ERCE appears a valuable starting platform to draw future evidence-based recommendations, overcoming the virtual impossibility to perform clinical trials on CE [24]. The need to enter CE cyst stages and clinical management decisions may also constitute a vehicle of knowledge of the WHO-IWGE staging and recommendations among the clinician’s community.

Learning from the past five years, in the near future the ERCE will be expanded to the online International Register of CE (IRCE) within the framework of the “PERITAS” project funded by the European platform EU-LAC Health ( and the National funding agencies of the participating institutions. The ERCE will be restructured into the IRCE aiming to answer relevant questions regarding the clinical management of CE.

Availability of data and materials

The datasets generated and analysed during the current study are not publicly available for personal data protection, in compliance with the Regulation (EU) 2016/679 and, formerly, with the Directive 96/46/EC, but are available from ERCE coordinators in a pseudonymized manner, subject to formal and motivated request and consent from relevant individual centres. All data are collected only upon obtainment of patient’s written consent, each Centre participating to the ERCE network owing data of patients registered in its institution.



cystic echinococcosis


European Centre for Diseases Prevention and Control


European Register of Cystic Echinococcosis


International Register of Cystic Echinococcosis


Registro Italiano dell’Echinococcosi Cistica (Italian Register of Cystic Echinococcosis)


World Health Organization


World Health Organization - Informal Working Group on Echinococcosis


  1. 1.

    WHO. Accelerating work to overcome the global impact of neglected tropical diseases—a roadmap for implementation. 2012. Geneva: World Health Organisation; 2012. Accessed 31 Mar 2019.

  2. 2.

    Casulli A, Siles-Lucas M, Tamarozzi F. Echinococcus granulosus sensu lato. Trends Parasitol. 2019;35:663–4.

    Article  Google Scholar 

  3. 3.

    Deplazes P, Rinaldi L, Alvarez Rojas CA, Torgerson PR, Harandi MF, Romig T, et al. Global distribution of alveolar and cystic echinococcosis. Adv Parasitol. 2017;95:315–493.

    Article  CAS  Google Scholar 

  4. 4.

    Budke CM, Deplazes P, Torgerson PR. Global socioeconomic impact of cystic echinococcosis. Emerg Infect Dis. 2006;12:296–303.

    Article  Google Scholar 

  5. 5.

    ECDC European Center for Disease Prevention and Control. Surveillance report—annual epidemiological report, food- and waterborne diseases and zoonoses. 2014. Accessed 31 Mar 2019.

  6. 6.

    Brundu D, Piseddu T, Stegel G, Masu G, Ledda S, Masala G. Retrospective study of human cystic echinococcosis in Italy based on the analysis of hospital discharge records between 2001 and 2012. Acta Trop. 2014;140:91–6.

    Article  Google Scholar 

  7. 7.

    Herrador Z, Siles-Lucas M, Aparicio P, Lopez-Velez R, Gherasim A, Garate T, et al. Cystic echinococcosis epidemiology in Spain based on hospitalization records, 1997–2012. PLoS Negl Trop Dis. 2016;10:e0004942.

    Article  Google Scholar 

  8. 8.

    van Cauteren D, Millon L, de Valk H, Grenouillet F. Retrospective study of human cystic echinococcosis over the past decade in France, using a nationwide hospital medical information database. Parasitol Res. 2016;115:4261–5.

    Article  Google Scholar 

  9. 9.

    EFSA and ECDC (European Food Safety Authority and European Centre for Disease Prevention and Control). The European Union summary report on trends and sources of zoonoses, zoonotic agents and food-borne outbreaks in 2017. EFSA J. 2018;2018(16):e05500.

    Google Scholar 

  10. 10.

    Commission Implementing Decision (EU) 2018/945 of 22 June 2018 on the communicable diseases and related special health issues to be covered by epidemiological surveillance as well as relevant case definitions. Accessed 21 Nov 2019.

  11. 11.

    Lissandrin R, Tamarozzi F, Mariconti M, Manciulli T, Brunetti E, Vola A. Watch and wait approach for inactive echinococcal cyst of the liver: an update. Am J Trop Med Hyg. 2018;99:375–9.

    Article  Google Scholar 

  12. 12.

    Stojkovic M, Rosenberger KD, Steudle F, Junghanss T. Watch and wait management of inactive cystic echinococcosis—does the path to inactivity matter—analysis of a prospective patient cohort. PLoS Negl Trop Dis. 2016;10:e0005243.

    Article  Google Scholar 

  13. 13.

    Tamarozzi F, Nicoletti GJ, Neumayr A, Brunetti E. Acceptance of standardized ultrasound classification, use of albendazole, and long-term follow-up in clinical management of cystic echinococcosis: a systematic review. Curr Opin Infect Dis. 2014;27:425–31.

    Article  CAS  Google Scholar 

  14. 14.

    Brunetti E, Kern P, Vuitton DA. Writing Panel for the WHO-IWGE. Expert consensus for the diagnosis and treatment of cystic and alveolar echinococcosis in humans. Acta Trop. 2010;114:1–16.

    Article  Google Scholar 

  15. 15.

    Nabarro LE, Amin Z, Chiodini PL. Current management of cystic echinococcosis: a survey of specialist practice. Clin Infect Dis. 2015;60:721–8.

    Article  Google Scholar 

  16. 16.

    Fasihi Harandi M, Budke CM, Rostami S. The monetary burden of cystic echinococcosis in Iran. PLoS Negl Trop Dis. 2012;6:e1915.

    Article  Google Scholar 

  17. 17.

    Narra R, Maestri M, Budke CM, Tamarozzi F, Mariconti M, Nicoletti GJ, et al. Costs associated with surgically treated cases of abdominal cystic echinococcosis: a single center’s experience from 2008 to 2014, Pavia, Italy. Am J Trop Med Hyg. 2016;95:405–9.

    Article  Google Scholar 

  18. 18.

    Tamarozzi F, Rossi P, Galati F, Mariconti M, Nicoletti GJ, Rinaldi F, et al. The Italian registry of cystic echinococcosis (RIEC): the first prospective registry with a European future. Euro Surveill. 2015;20:21115.

    Article  Google Scholar 

  19. 19.

    Rossi P, Tamarozzi F, Galati F, Pozio E, Akhan O, Cretu CM, et al. The first meeting of the European Register of Cystic Echinococcosis (ERCE). Parasit Vectors. 2016;9:243.

    Article  Google Scholar 

  20. 20.

    Tamarozzi F, Akhan O, Cretu CM, Vutova K, Akinci D, Chipeva R, et al. Prevalence of abdominal cystic echinococcosis in rural Bulgaria, Romania, and Turkey: a cross-sectional, ultrasound-based, population study from the HERACLES project. Lancet Infect Dis. 2018;18:769–78.

    Article  Google Scholar 

  21. 21.

    Piseddu T, Brundu D, Stegel G, Loi F, Rolesu S, Masu G, et al. The disease burden of human cystic echinococcosis based on HDRs from 2001 to 2014 in Italy. PLoS Negl Trop Dis. 2017;11:e0005771.

    Article  Google Scholar 

  22. 22.

    United Nations High Commission for Refugees UNHCR. Global trends. Forced displacement in 2017. Accessed 21 Nov 2019.

  23. 23.

    Richter J, Esmann L, Lindner AK, Trebesch I, Equihua-Martinez G, Niebank M, et al. Cystic echinococcosis in unaccompanied minor refugees from Afghanistan and the Middle East to Germany, July 2016 through June 2017. Eur J Epidemiol. 2019;34:611–2.

    Article  Google Scholar 

  24. 24.

    Meeting of the WHO Informal Working Group on Echinococcosis (WHO-IWGE), Geneva, Switzerland, 15–16 December 2016 (WHO/HTM/ NTD/NZD/2017.01). Geneva: World Health Organization; 2017. Accessed 31 Mar 2019.

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We are thankful to all the people contributing to data collection in the ERCE. We also thank Dr Belgees Boufana for editing the English.

Additional members of ERCE network and their affiliations at the time of last patient entry are:

A. Angheben (Sacro Cuore Hospital Negrar, Verona, Italy); M. Belhassen Garcia (Salamanca University Hospital, Research Center of Tropical Diseases of University of Salamanca, Salamanca, Spain); N. Bagmet (Russian Scientific Center of Surgery B.V. Petrovsky, Moscow, Russia); S. Borys (University Center of Maritime and Tropical Diseases, Gdynia, Poland); S. Bresson-Hadni, F. Demonmerot and L. Millon (National Reference Center for Echinococcosis, University Hospital Besançon, France); F. Bruschi (N.T.M.C. Pisa University, Pisa, Italy); G. Calleri (Amedeo di Savoia Hospital, Turin, Italy); C. Chemla (Regional Hospital Center and University of Reims (CHU), Parasitology Laboratory, Biology Center, Reims, France); B. Castiglioni (San Raffaele Hospital, Milan, Italy); L. G. Chianura (Niguarda Ca’ Granda Hospital, Milan, Italy); B. Dezsényi (Central Hospital of Southern Pest National Institute of Haematology and Infectious Diseases, Budapest, Hungary); M. F. Harandi and Saeid Nasibi (Research Center for Hydatid Disease in Iran, Kerman University of Medical Sciences, Kerman, Iran); G. Ismailova (National Scientific Center of Surgery named “A. Syzganov”, Almaty, Kazakhstan); M. T. Giordani (Department of Infectious and Tropical Diseases, Veneto ULSS 6, Vicenza, Italy); V. Gjoni and R. Shkjezi (Institute of Public Health, Tirana, Albania); L. Gogichaishvili (S. Virsaladze Research Institute of Medical Parasitology and Tropical Medicine, Tbilisi, Georgia); D. Goletti (National Institute for Infectious Diseases L. Spallanzani-IRCCS, Rome, Italy); F. Karim (Mitford Hospital, Dhaka, Bangladesh); E Lapini (S. Donato Hospital, Arezzo, Italy); S. Mastrandrea (University Hospital, Sassari, Italy); F. Lötsch (Medical University of Vienna, Vienna, Austria); G. Menozzi and R. Corsini (Santa Maria Nuova Hospital IRCCS, Reggio Emilia, Italy); P. Milhailescu (Colentina Clinical Hospital, Bucharest, Romania); S. Orsten (Hacettepe University, School of Health Services, Ankara, Turkey); A. Paugam (University Hospitals Paris Center (AP-HP), Cochin Hospital, Paris, France); M. Ramharter (Medical University of Vienna, Vienna, Austria and Department of Tropical Medicine, Bernhard Nocht Institute for Tropical Medicine & I. Dep. of Medicine, University Medical Center Hamburg-Eppendorf); A. Recordare (Regional Hospital Ca’ Foncello, Treviso, Italy); F Salvador (Infectious Diseases Department, Vall d’Hebron University Hospital, PROSICS Barcelona, Spain); A. Teggi (S. Andrea Hospital, Rome, Italy); C. Torti (AOU Mater Domini, Catanzaro, Italy); G. Vitale (A.O.U.P. Paolo Giaccone, Palermo, Italy); A. Vola, M. Mariconti and R. Lissandrin (Division of Tropical and Infectious Diseases, San Matteo Hospital Foundation, Pavia, Italy); M. Wallon (Civil Hospices of Lyon, Lyon University, Lyon, France); L. Zammarchi and F. Bartalesi (Careggi University Hospital, Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy).


RIEC development received funding through the Research Project IZSSA07/10RC to Dr. Giovanna Masala (Sardinian Experimental Zooprophylactic Institute, Sassari, Italy), subcontracted to Enrico Brunetti, University of Pavia, Italy. The amendment of RIEC and development of the ERCE was funded through the European Commission, under the Seventh Framework Programme (FP7, Theme Health.2013.2.3.4-1, grant agreement. no. 602051, Project HERACLES: Human Cystic Echinococcosis ReseArch in Central and Eastern Societies; to Adriano Casulli, Istituto Superiore di Sanità, Rome, Italy. ERCE activities are currently supported by EU-LAC Health ( and the Italian Ministry of Health - PERITAS project (molecular ePidemiological studiEs on pathways of tRansmIssion and long lasTing cApacity building to prevent cyStic echinococcosis infection) to Adriano Casulli, Istituto Superiore di Sanità, Rome, Italy.

Author information





PR and AC conceived the manuscript; PR, FT and FG extracted the data; PR and FT analysed the data and drafted the manuscript, AC edited the manuscript and received funding for this research; PR, FT, OA, CMC, KV, MSL, EB and the ERCE network participants inserted data and/or managed the database; all authors critically revised and approved the submitted version of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Adriano Casulli.

Ethics declarations

Ethics approval and consent to participate

RIEC was approved by the Ethics Committee of the Istituto Superiore di Sanità, Rome, Italy with protocol N CE/12/347 followed by extended approval to the ERCE with protocol N PRE-C-915/14. Ethical approval from the relevant Ethics Committee (local or national depending on the country) was obtained by all physicians/centres, as a requirement to start accessing the register. Patients, or the legal representative for minors, were asked written informed consent at first registration.

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Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Supplementary information

Additional file 1: Table S1.

Country of birth for patients registered in ERCE centres. Table S2. Clinical management of cysts by stage and location.

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Rossi, P., Tamarozzi, F., Galati, F. et al. The European Register of Cystic Echinococcosis, ERCE: state-of-the-art five years after its launch. Parasites Vectors 13, 236 (2020).

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  • Cystic echinococcosis
  • Register
  • Public health awareness
  • Case series