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Alergol Inmunol Clin 2000;15:230-236<br />

Mª C. López Serrano,<br />

A. Alonso-Gómez,<br />

Á. Moreno-Ancillo 1 ,<br />

Á. Daschner,<br />

J. Suárez de Parga 1<br />

Allergy Section and<br />

1<br />

Endoscopy Unit, "La Paz"<br />

General University Hospital.<br />

Madrid, Spain<br />

Original Article<br />

<strong>Gastroallergic</strong> <strong>anisakiasis</strong>: <strong>immediate</strong><br />

hypersensitivity due to Anisakis simplex<br />

infestation<br />

In Spain, cases of <strong>anisakiasis</strong> were anecdotic up to 1995. In that year, however,<br />

and led by Dr. Fernández de Corres, the Spanish allergologists became<br />

fully aware of Anisakis simplex (AS) because of cases of allergic reaction<br />

after the intake of "presumably" well-cooked fish with positive skin<br />

tests and specific IgE to AS. The fundament of AS allergy appeared to reside<br />

in the heat stability of AS antigens. Following the observation of several<br />

cases of anaphylaxis with AS infestation, a prospective study was set<br />

up in 1997 in the "La Paz" University Hospital. Patients were entered into<br />

the study that came to the Emergency Outpatient Clinic with allergic or<br />

gastrointestinal symptoms after the ingestion of seafoods or fish up to 48<br />

hours earlier. If the gastrointestinal symptoms persisted, a gastroscopy was<br />

performed. Over a period of 18 months, 120 patients were assessed who<br />

complained of allergic symptoms; in 96 of them, AS was actually implicated.<br />

Over those 18 months, and based on the allergic symptoms, 24 patients<br />

were detected in whom one or more parasites were removed from their stomachs<br />

(more parasites detected within 18 months than in the whole of<br />

Spain since 1991). Vinegar-marinated herring and in some cases fresh hake<br />

-presumably well-cooked- were the sources in most of the cases of parasitic<br />

infestation. The authors coined for this condition the term gastroallergic<br />

<strong>anisakiasis</strong> in order to differentiate it from gastric <strong>anisakiasis</strong>, as the hypersensitivity<br />

symptoms after contact with the parasite were more intense and<br />

severe than the gastric ones. The antigenic source appeared to be in most<br />

cases the live parasite, and, furthermore, it appeared to require binding to<br />

the submucosa in order to trigger the hypersensitivity reaction.<br />

The next step in these patients with gastroallergic <strong>anisakiasis</strong> was to carry<br />

out challenge tests with frozen, non-infective parasites. Tolerance was<br />

confirmed in a number of patients, and from then onwards patients were<br />

allowed to eat deep-frozen fish, with no problems ensuing. At that point,<br />

allergy to heat-stable AS proteins appeared to be less frequent than previously<br />

supposed, and it was surmised that the IgE-mediated response corresponded,<br />

in most sensitised patients, to contact (luminal or asymptomatic<br />

parasitic infestations) with the live parasite.<br />

The past history of dietary intake, the clinical features, the skin test responses<br />

and the serial quantitation of AS-specific IgE represent important key points in<br />

the diagnosis. Cases of true Anisakis simplex allergy may indeed exist, but in<br />

the light of the results of this prospective study they appear to be infrequent.<br />

Key words: Anisakis simplex. <strong>Gastroallergic</strong> <strong>anisakiasis</strong>. Prospective study.<br />

230


<strong>Gastroallergic</strong> <strong>anisakiasis</strong><br />

Anisakiasis gastro-alérgica:<br />

hipersensibilidad inmediata debida<br />

a parasitación por Anisakis<br />

simplex<br />

En España, hasta 1995 los casos de <strong>anisakiasis</strong> eran anecdóticos.<br />

Sin embargo, en 1995, los alergólogos españoles, de la<br />

mano del grupo del Dr. Fernández de Corres, llegan al Anisakis<br />

simplex (AS) por casos de reacciones alérgicas tras consumo<br />

de pescado "presumiblemente" bien cocinado y con pruebas<br />

cutáneas e IgE específica a AS positivas. La base de la<br />

alergia al AS parecía estar en la termoestabilidad de antígenos<br />

del AS. Tras observar algunos casos de anafilaxia con<br />

parasitación por AS, en 1997 se inició en el Hospital Universitario<br />

"La Paz" de Madrid un estudio prospectivo. Se introdujeron<br />

pacientes que acudían a Urgencias con síntomas alérgicos<br />

o gastrointestinales tras ingestión de productos de mar,<br />

aceptando pacientes que hubieran tomado el alimento hasta<br />

48 horas antes. Si el cuadro digestivo persistía se realizaba<br />

endoscopia. En 18 meses se evaluaron 120 pacientes que<br />

consultaron por síntomas alérgicos, de los cuales en 96 se implicó<br />

verdaderamente al AS. En esos 18 meses, y sobre la base<br />

de los síntomas de alergia, se detectaron 24 pacientes a los<br />

que se extrajeron del estómago uno o más parásitos (más parásitos<br />

hallados en sólo 18 meses que desde 1991 en España).<br />

El boquerón en vinagre y, en algunos casos, la merluza fresca,<br />

presumiblemente bien cocinada, fueron la fuente de la<br />

mayoría de las parasitaciones. Los autores denominaron a esta<br />

entidad <strong>anisakiasis</strong> gastro-alérgica, diferenciándola de la<br />

<strong>anisakiasis</strong> gástrica dado que los síntomas de hipersensibilidad<br />

tras el contacto con el parásito eran más intensos e importantes<br />

que los gástricos. Parecía que, en su mayoría, era el<br />

parásito vivo la fuente antigénica, y, más aún, que necesitaba<br />

fijarse a la submucosa para producir la reacción de hipersensibilidad.<br />

El paso siguiente en estos pacientes con <strong>anisakiasis</strong><br />

gastro-alérgica fue la provocación con parásitos congelados<br />

no infectivos. Se confirmó su tolerancia en varios pacientes,<br />

y a partir de entonces al resto se les permitió comer pescado<br />

congelado sin suceder ningún problema. En ese punto, la<br />

alergia a proteínas termoestables del AS parecía menos frecuente<br />

de lo previamente supuesto, y se intuía que la respuesta<br />

mediada por IgE en la mayoría de los pacientes sensibilizados<br />

correspondía a contactos (parasitaciones en forma<br />

luminal o asintomáticas) con el parásito vivo. El antecedente<br />

dietético, la clínica, la respuesta a las pruebas cutáneas y la<br />

medición seriada de IgE específica a AS son claves importantes<br />

para el diagnóstico. Puede que existan casos de verdadera<br />

alergia a AS, pero a la vista de los resultados del presente<br />

estudio prospectivo deben ser infrecuentes.<br />

Palabras clave: Anisakis simplex. Anisakiasis gastro-alérgica.<br />

Estudio prospectivo.<br />

INTRODUCTION<br />

Anisakis simplex (AS) is a parasitic helminth included<br />

in the Class Nematoda. Leucckart, in 1876, was the<br />

first to describe a case of human infestation, in a Greenland<br />

child. In 1960, Van Thiel identified the infesting parasite<br />

as the stage III larva of Anisakis 1-5 . The taxonomy of<br />

the genus Anisakis is a complex one. It is included in the<br />

Class Nematoda, subclass Secernentea, order Ascaridida,<br />

suborder Ascaridina, superfamily Ascaridoidea, family<br />

Anisakidea. The subfamily Anisakinae includes the genus<br />

Anisakis, with four recognised species: Anisakis simplex,<br />

Anisakis physeris, Anisakis typica and Anisakis schupakovi<br />

5 . All these species are usually parasitic in the stomach of<br />

marine mammals. The life cycle of the parasite may include<br />

one or more intermediate hosts. The ova of the adult parasites<br />

are shed with the marine mammal’s faeces into the<br />

water and continue there their development up to the stage<br />

of infective larva. At this stage, the larva is some 0.35 mm<br />

long and is ingested by a first host, usually planktonic<br />

crustaceans, in which it develops further and attains a size<br />

of about 5 mm. After a fish or a cephalopod has ingested<br />

the crustacean host, the larvae develop into their third larval<br />

stage and grow to about 2-3 cm in length. These larvae<br />

may pass several times from one fish or cephalopod to<br />

another one, but they do not complete their evolutive cycle<br />

until they arrive into the stomach of a marine mammal.<br />

There they attach themselves to the gastric wall and evolve<br />

into the fourth larval stage and then into adult parasites,<br />

thus completing their life cycle 1-5 .<br />

Man is an aberrant host, as the larva cannot attain sexual<br />

maturity in this environment. Man becomes infested<br />

upon ingesting the larvae in raw or undercooked fish, but<br />

also in smoked fish, semi-preserves, dried or marinated<br />

fish (particularly vinegar-marinated), ceviche (a Peruvian<br />

lemon-marinated fish preparation) or Japanese culinary delicacies<br />

such as sushi or sashimi, which are prepared with<br />

raw fish. The number of fish species reported to be pos-<br />

231


M. a C. López Serrano, et al<br />

sibly infested is a veritable host, and includes cod, sardine,<br />

herring, mackerel, salmon, hake, pollack, anchovy, whiting,<br />

bonita and horse mackerel; the most frequently infested<br />

cephalopod is the squid 6-9 .<br />

Parasitic infestation of man by the live larvae is termed<br />

<strong>anisakiasis</strong> or anisakidosis, and is particularly common<br />

among the Japanese because of their habit of raw fish<br />

consumption 10,11 .<br />

By the year 1995, human Anisakis-related diseases<br />

were differentiated into a number of clinical forms depending<br />

on the affected region of the digestive tract. The<br />

luminal form was considered to be caused only by Phocanema<br />

larvae and to constitute a lesser stage in which<br />

only asymptomatic adherence of the larvae occurred. In<br />

these cases, the larvae die within a period of weeks and<br />

are expelled with the faeces 12 . A further form was gastric<br />

<strong>anisakiasis</strong>, caused by stage III larvae and characterised<br />

by epigastric pain episodes 13-16 . If the parasite was not extracted,<br />

the disease could progress towards the invasive<br />

forms of subacute or chronic <strong>anisakiasis</strong> 17-20 . There had<br />

also been some reports of polyarthritis 21,22 and some rare<br />

cases of invasion of other organs such as the lung, liver,<br />

spleen and pancreas 23 . In these cases of advanced <strong>anisakiasis</strong>,<br />

IgE and eosinophils had been implicated in the<br />

pathogenesis of the local lesions caused by the parasite<br />

16,24-29 . Only occasionally had localised maculopapular<br />

lesions or generalised urticaria been reported in these patients<br />

13,23,30 .<br />

At that time, and up to 1996, many cases had already<br />

been reported in the Netherlands and occasional ones in<br />

France, the United Kingdom and the USA 3,4,11,20,31,32 . In<br />

Spain, only anecdotal cases of <strong>anisakiasis</strong> had been published<br />

between 1991 and 1996 21,33-35 .<br />

In 1995, Spanish allergologists finally began paying<br />

attention to Anisakis-induced disease because of reported<br />

cases of allergic reactions after the intake of presumably<br />

well-cooked fish in association to positive skin tests and<br />

specific IgE for Anisakis, while the investigations were negative<br />

for the fish supposedly involved in the reaction. Some<br />

authors postulated that the fundament of Anisakis simplex<br />

allergy was the heat-stability of a number of antigens<br />

that might be able to bind to the patients’ IgE and trigger<br />

hypersensitivity symptoms upon the ingestion of cooked<br />

fish 38-40 .<br />

After having observed some cases of anaphylaxis<br />

with Anisakis simplex infestation 42 , a prospective study was<br />

begun in 1997 at the "La Paz" University Hospital in Madrid<br />

(Spain).<br />

MATERIAL AND METHODS<br />

Patients were entered into the study who were seen<br />

at the Emergency Outpatient Clinic because of<br />

allergic or gastrointestinal symptoms after the ingestion<br />

of fish or seafood, irrespective of the preparation,<br />

and including patients who had eaten the suspect food<br />

up to 48 hours earlier. Endoscopy was performed if the<br />

digestive symptoms persisted for over 6-8 hours. In all<br />

patients entered, skin tests were performed with Anisakis<br />

extract, with a panel of different fishes and with<br />

the particular fish or seafood apparently involved in<br />

the reaction. The total serum and fish- and Anisakis<br />

simplex-specific IgE levels were also measured during<br />

the acute episode, and the total IgE and Anisakisspecific<br />

IgE were again measured one month after the<br />

reaction.<br />

RESULTS<br />

Over a period of 18 months, 120 patients consulting<br />

because of allergic symptoms were studied; in 96 of them<br />

Anisakis simplex was actually involved. The associated digestive<br />

symptoms were mild or moderate in most patients,<br />

so that endoscopy was performed only in 47 of them. In<br />

that period 24 infested patients were detected in whom<br />

one or more parasites were removed from the stomach at<br />

endoscopy.<br />

The patient population was divided into three<br />

groups:<br />

1) Patients who had undergone endoscopy and were<br />

actually infested.<br />

2) Patients who had undergone endoscopy and were<br />

not infested.<br />

3) Patients who had not undergone endoscopy.<br />

Vinegar-marinated anchovies and, in some cases,<br />

presumably well-cooked fresh hake were the sources of<br />

most parasitic infestations.<br />

The latency period of the allergic symptoms was variable,<br />

with a mean latency of ca. 6 hours but with a range<br />

between minutes and over 24 hours, and with no differences<br />

between the three groups.<br />

In many cases the digestive symptoms had already<br />

subsided, and endoscopy was not performed.<br />

The total serum and specific IgE levels were significantly<br />

increased one month after contact with the parasite<br />

in all three groups.<br />

232


<strong>Gastroallergic</strong> <strong>anisakiasis</strong><br />

The statistical analysis of the characteristics of the<br />

three patient groups suggests that they were composed of<br />

similar patients.<br />

CHALLENGE TESTS AND LATER DIET<br />

Over the time of the study no clearly defined cases<br />

were seen of patients having had symptoms either with<br />

deep-frozen fish (industrial preparations) or with sufficiently<br />

cooked fish preparations. It is an axiom in Allergology<br />

that, when doubts arise as to a given allergen being<br />

the cause of a given reaction, challenge tests with that<br />

allergen are proposed, besides the usual in vitro assessments<br />

and skin tests.<br />

Live parasites were frozen until they became non-infective.<br />

Challenge tests were then performed, initially giving<br />

from 11 to 20 parasites to a total of 20 out of the 96<br />

patients, with negative results. The challenge tests were<br />

thereupon interrupted, and the remainder of the patients<br />

were allowed to eat deep-frozen fish or seafoods; the tolerance<br />

was repeatedly checked in successive six-monthly<br />

visits and up to the time of writing. In a total of 76 patients<br />

so investigated, no problem related to the ingestion<br />

of deep-frozen fish has been detected until now. Twenty<br />

patients were lost to follow-up, as they did not attend the<br />

successive review visits.<br />

DISCUSSION<br />

In 1995, the conditions caused by Anisakis simplex<br />

were differentiated into a number of clinical forms according<br />

to the digestive tract region involved. Gastric <strong>anisakiasis</strong><br />

was caused by stage III larvae; in this particular<br />

form the larvae reach the submucosa through the action of<br />

peptidases, and induce epigastric pain due to the inflammatory<br />

reaction of the viscus wall 13-16 . If the parasite(s) were<br />

not extracted, the condition progressed to the subacute or<br />

chronic <strong>anisakiasis</strong> form. The larvae might be able to traverse<br />

the gastric or intestinal wall; the parenteral invasive<br />

form resulting might cause granulomata or abscessification<br />

in association to eosinophilia, fever, diarrhoea and abdominal<br />

pain. This situation might mimic acute appendicular<br />

episodes, but true appendicitis and episodes of intestinal<br />

obstruction had also been reported 17-20 . Infrequent cases of<br />

polyarthritis 21,22 and still rarer ones of distant organ invasion<br />

(lung, liver, spleen and pancreas) 23 had also been described.<br />

In these cases of <strong>anisakiasis</strong>, both the IgE and the<br />

eosinophils had been implicated in the aetiopathogenesis<br />

of the local lesions caused by the attachment of the parasites<br />

16,24-29 . In the course of a first contact, the parasitic infestation<br />

might induce a mild chronic inflammatory reaction<br />

in the mucosa. The acute forms would then be due<br />

to type I or type III hypersensitivity reactions in the digestive<br />

tract in the course of secondary infestations 16,29,30 .<br />

Only occasionally had localised maculopapular lesions<br />

and generalised urticaria been reported in these patients<br />

13,23,30 .<br />

In Europe, and up to 1996, over 100 cases had been<br />

reported in the Netherlands (collected between 1995 and<br />

1968) 3,4,11 ; and there had been occasional case reports in<br />

France, the United Kingdom and the USA from 1975 onwards<br />

11,20,31,32 . In Spain, some six cases had been reported<br />

between 1991 and 1996; cases of <strong>anisakiasis</strong> were anecdotal<br />

at that time 21,33-35 , but from that year onwards the number<br />

of reports increased progressively.<br />

In 1995 the Spanish allergologists were made aware<br />

of Anisakis-induced disease through cases of allergic reactions<br />

after the ingestion of presumably well-cooked fish<br />

with positive skin tests and specific IgE to Anisakis while<br />

the studies were negative for the fish supposedly involved<br />

in the reaction 36-41 . The reports of Anisakis simplex sensitisation<br />

multiplied, and some confusion arose regarding the<br />

value of some positive tests in patients describing no allergic<br />

reaction at all, and of course no previous infestation<br />

by Anisakis simplex (ca. 13%). For some authors, the basis<br />

of Anisakis simplex allergy was to be found in the heatstability<br />

of some antigens of the parasite, which would be<br />

able to bind to the patients’ IgE and trigger hypersensitivity<br />

symptoms upon the ingestion of cooked fish 38-40 .<br />

After having observed a number of cases of anaphylaxis<br />

associated to Anisakis simplex infestation 42 , a prospective<br />

study was initiated at the "La Paz" University<br />

Hospital in Madrid. Over a period of 18 months 120 patients<br />

were assessed, who had consulted because of allergic<br />

symptoms (in many cases life-threatening anaphylaxis<br />

or anaphylactic shock); in 96 of them Anisakis simplex<br />

was truly implicated in the reactions 43-49 . The associated digestive<br />

symptoms were mild or moderate in most patients,<br />

and for this reason only 47 patients underwent endoscopy.<br />

To our surprise, over those 18 months, and based on the<br />

allergic symptoms, 24 patients were detected in whom one<br />

or more parasites were removed from their stomachs (almost<br />

more parasites found over a period of 18 months<br />

than in the whole of the Spanish literature between 1991<br />

233


M. a C. López Serrano, et al<br />

and that time). The very typical "boquerón en vinagre"<br />

(vinegar-marinated anchovies) and in some cases presumably<br />

well-cooked fresh hake were the sources of most<br />

infestations. The latency period of the allergic symptoms<br />

was quite variable, ranging between a few minutes and<br />

over 24 hours. The average latency for the digestive<br />

symptoms was similar, although they tended to occur<br />

slightly earlier. No endoscopy was performed when the digestive<br />

symptoms had already subsided at the time of seeing<br />

the patient. The total serum IgE and the specific IgE<br />

were found to be significantly increased one month after<br />

the index contact 45,47,48 .<br />

The statistical analyses suggested that the study population<br />

was formed by similar patients, in whom in some<br />

cases the parasite became attached to the gastric mucosa<br />

for a time sufficient for triggering the allergic reaction;<br />

however, its trend to then detach and be expelled does not<br />

allow it to be detected in time at endoscopy. The authors<br />

termed this particular condition gastroallergic <strong>anisakiasis</strong>"<br />

42-51 , differentiating it from gastric <strong>anisakiasis</strong>, as the<br />

hypersensitivity symptoms after contact with the parasite<br />

were more intense and severe than the gastric ones. However,<br />

in the course of the study period and also in a review<br />

of previous suggestive cases from our Hospital no cases<br />

were detected in which symptoms had arisen after consuming<br />

industrially deep-frozen or sufficiently cooked fish.<br />

In the light of this observation, it would appear that in<br />

most cases the live parasite had been the antigen source,<br />

and furthermore, that the parasite required attachment to<br />

the submucosa in order to elicit the hypersensitivity reaction.<br />

At this point in time, true allergy to heat-stable proteins<br />

of Anisakis simplex appeared to be less frequent than<br />

previously supposed, and it was thought that the IgE-mediated<br />

response corresponded, in most of the sensitised patients,<br />

to previous contacts with the live parasite (transient<br />

infestation either in the luminal form or clinically asymptomatic).<br />

Adhering to the diagnostic procedure usually applied<br />

in Allergology whenever there is doubt about a given antigen<br />

as the cause of a given reaction, the next step in these<br />

patients with gastroallergic <strong>anisakiasis</strong> was challenge testing<br />

with non-infective frozen parasites 50 . Tolerance was<br />

confirmed in a number of patients, and from then onwards<br />

the remainder of the patients were allowed to eat deep-frozen<br />

fish, with no untoward problems arising.<br />

The immunologic and inflammatory response to the<br />

parasite may explain most of the clinical symptoms and<br />

signs in <strong>anisakiasis</strong>. The parasite avails itself of proteases<br />

in order to achieve attachment to the gastrointestinal mucosa.<br />

It is quite possible that local factors such as preexisting<br />

mucosal lesions, changes in gastrointestinal motility<br />

or changes in the environmental pH may influence not<br />

only the parasite’s ability to become attached but also the<br />

duration of such attachment end even the possibility –rather<br />

more remote, but already reported– of transmucosal<br />

penetration. Once attached to the submucosa, the secretion<br />

of proteins by the parasite sets in motion the defensive<br />

response of the rich gastrointestinal lymphoid tissue. The<br />

type of anti-parasite response in this case is predominantly<br />

Th2. Thus, the expression pattern of cytokines such as IL-4<br />

and IL-5 leads to chemotactic attraction of eosinophils and<br />

to intestinal lymphoid tissue hyperplasia and also to a stimulation<br />

to IgE production, with the subsequent increase<br />

of the total and parasite-specific IgE levels 16,24-29,48 . Other<br />

immunoglobulins are also produced and may in some cases<br />

lead to immune-complex-mediated responses.<br />

The symptomatology of <strong>anisakiasis</strong> would be mediated<br />

mainly by this inflammatory response and in some cases<br />

by the penetration of the parasite. If the response is<br />

maintained only in the local gastric environment, acute<br />

gastric <strong>anisakiasis</strong> will ensue. Further to this, the already<br />

initiated immune response may induce distant hypersensitivity<br />

symptoms mediated by IgE –and therefore allergic–,<br />

which seem to be rather frequent: gastro-allergic <strong>anisakiasis</strong>.<br />

Immune complexes might explain the articular manifestations<br />

sometimes observed but, in the light of the published<br />

reports, are rather infrequent. Subacute or chronic<br />

<strong>anisakiasis</strong> is usually seen at the intestinal level, and the<br />

inflammation (even though the parasite may have already<br />

been expelled with the faeces) may induce mucosal changes<br />

leading even to an acute abdomen. If the parasite still<br />

remains within the digestive tract wall, or even achieves<br />

its penetration, surgery will be required in most of these<br />

cases. In very rare cases, penetration of the parasite leads<br />

to its apparition in exceptional locations such as the lung,<br />

the liver, the spleen or the pancreas.<br />

In the cases of subacute or chronic <strong>anisakiasis</strong>, distant<br />

hypersensitivity manifestations are infrequent.<br />

The previous history of fish or seafood ingestion, the<br />

clinical manifestations, the endoscopic and radiologic examination,<br />

the response to the skin tests and the serial measurements<br />

of the specific IgE Anisakis simplex antibodies<br />

are important clues for the diagnosis.<br />

Cases may exist of true Anisakis simplex allergy but,<br />

in the light of the results of this prospective study, they<br />

234


<strong>Gastroallergic</strong> <strong>anisakiasis</strong><br />

should not be particularly frequent. Challenge tests with<br />

non-infective parasites should be the clue for diagnosis in<br />

these cases, keeping in mind the importance of the subsequent<br />

dietary restrictions 50,52 .<br />

The best therapeutic measure for <strong>anisakiasis</strong> is<br />

prophylaxis and prevention, avoiding the ingestion of raw<br />

fish or of fish prepared in ways that do not extinguish the<br />

viability of the larvae. Industrial smoking should achieve<br />

temperatures of at least 60ºC for at least 10 minutes if it is<br />

to be considered safe. The larvae may withstand conditions<br />

such as 50 days at 2ºC, 60 days in vinegar, 6 days in formaldehyde,<br />

or 2 hours at –20ºC. however, they are unable<br />

to resist over 2 minutes at temperatures in excess of 60ºC.<br />

The infestation rates of fish are high, ranging from<br />

40 to 80% of the pieces examined depending on the species<br />

6-9 . The prophylactic measure imposed by law within<br />

the European Union, that is to compulsorily deep-freeze<br />

any fish destined to commercialisation for raw consumption<br />

to –20ºC for at least 24 hours, has dramatically reduced<br />

the incidence of <strong>anisakiasis</strong> in many regions in Europe.<br />

In Spain, the main problems resides in the lack of<br />

information on the side of the home cooks or of the restauration<br />

industry, so that the fish that has been bought<br />

and prepared either raw or undercooked not necessarily<br />

has complied with that ruling.<br />

The observation by the Allergologists has only made<br />

manifest (and put a name) one disease condition that has<br />

probably existed for a long time 42-51 . Because of this renewed<br />

vigilance, there is a continuing increase of the number<br />

of cases reported in Spain, where preventive rulings<br />

that do exist are not sufficiently applied.<br />

REFERENCES<br />

1. Gibson DI. The systematics of Ascaridoid Nematodes. A current<br />

assessment. En Stone AR, Platt HM, Khalil LF eds. Concepts in nematode<br />

systematics. London: Academic press, 1983; 321-338.<br />

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