Late recrudescence of Plasmodium falciparum malaria in a pregnant woman: a case report
Notice bibliographique
Résumé
More than 90% of imported Plasmodium falciparum malaria infections are diagnosed within five weeks after returning from an endemic area.1Legros F. Gay F. Belkaid M. Danis M. Paludisme in France Métropolitaine en 1996. Centre National de Référence pour les Maladies d’Importation.Bullettin du CNRMI. 1997; 13: 1-60Google Scholar, 2Krajden S. Panisko D.M. Tobe B. Yang J. Keystone J.S. Prolonged infection with Plasmodium falciparum in a semi-immune patient.Trans R Soc Trop Med Hyg. 1991; 85: 731-732Abstract Full Text PDF PubMed Scopus (27) Google Scholar Here a case of P. falciparum malaria in a pregnant woman is reported, diagnosed four years after her last stay in an endemic area. A pregnant 29-year-old Ghanaian woman having lived in Italy for eight years was seen in November 2001. Her last visit to Ghana had been in summer 1997 and she had not taken anti-malarial prophylaxis and remained apyrexial during the following months. In August 2001 she developed fever, headache and vomiting, initially interpreted as gravidic hyperemesis. The thick and thin blood films showed trophozoites and gametocytes of P. falciparum (PF) (5350 trophozoites × 106/L). A PCR was not carried out, but a rapid antigen detection test (Binax NOW® ICT Pf/Pv test) and the anti-PF antibody test (IFAT, BioMérieux) were positive (>1/1280 versus 1/20 normal). The microscopy was confirmed by two referral centres in Italy and by the Prince Leopold Institute of Tropical Medicine in Antwerp, Belgium. The patient was treated intravenously with quinine for six days after which the symptoms rapidly disappeared and she was discharged in good conditions. The pregnancy progressed normally. The normal incubation of P. falciparum malaria is 7–15 days3Gentilini M. Paludisme, Médicine Tropicale; Paris: Editions Flammarion; 1995, p. 94.Google Scholar and recrudescence is possible within a few weeks to one year after an untreated or incompletely treated infection. However, cases of late P. falciparum infection have been reported.2Krajden S. Panisko D.M. Tobe B. Yang J. Keystone J.S. Prolonged infection with Plasmodium falciparum in a semi-immune patient.Trans R Soc Trop Med Hyg. 1991; 85: 731-732Abstract Full Text PDF PubMed Scopus (27) Google Scholar, 4Verdrager J. Observation of the longevity of Plasmodium falciparum: with special reference to findings in Mauritius.Bull WHO. 1964; 31: 747-751PubMed Google Scholar, 5Eloy O. Zuily E. Greder-Belan A. Bouchot C. Ghnassia J.C. Legros F. Paludisme à Plasmodium falciparum quatre ans après le retour de zone d’endémie.Presse Med. 1998; 27: 189PubMed Google Scholar, 6Duperval R. Longpré B. Madamas P. Unexplained falciparum malaria in a patient with chronic lymphocytic leukaemia.Can Med Assoc J. 1979; 121: 1585-1588PubMed Google Scholar, 7Besson P. Robert J.F. Reviron J. Richard-Lenoble D. Gentilini M. Two cases of transfusional malaria.Rev Fr Transfus Immunohematol. 1976; 19: 369-373Crossref PubMed Scopus (22) Google Scholar, 8Slinger R. Giulivi A. Bodie-Collins M. Hindieh F. St John R. Sher G. et al.Transfusion transmitted malaria in Canada.Can Commun Dis Rep. 1999; 25: 53-56PubMed Google Scholar The present patient had never used intravenous drugs nor received any blood transfusion or parenteral treatment. Potential vectors of Plasmodium vivax are still present in some rural areas of central and southern Italy,9Romi R. Sabatinelli G. Majori G. Could malaria reappear in Italy?.Emerg Infect Dis. 2001; 6: 915-919Crossref Scopus (61) Google Scholar however, this patient lived in an urban area of northern Italy. She had not travelled by air since 1997 so airport malaria and “baggage” malaria were also excluded. The patient used to receive packages from Ghana, which could have evaded regular health controls,10Castelli F. Caligaris S. Matteelli A. Chiodera A. Carosi G. Fausti G. Baggage malaria in Italy: cryptic malaria explained?.Trans R Soc Trop Med Hyg. 1993; 87: 394Abstract Full Text PDF PubMed Scopus (21) Google Scholar but the last one had arrived before her last journey to Africa. The most likely hypothesis is that the patient was infected during her last stay in Ghana in 1997. The infection was sub-clinical because of premunition. By impairing the pre-existing immune equilibrium,11Rasheed F.N. Bulmer J.N. De Francisco A. Jawla M.F. Jakobsen P.H. Jepson A. et al.Relationships between maternal and malarial immune responses in mothers and neonates.Parasite Immunol. 1995; 17: 1-10Crossref PubMed Scopus (61) Google Scholar pregnancy could have acted as a trigger of an extremely late recrudescence of P. falciparum malaria. This case highlights the problem of malaria transmitted by blood transfusion, which represents a rare but serious complication of blood transfusion in the United States (estimated incidence lower than 0.3 cases per million transfused blood units).12CDC Transfusion-transmitted malaria – Missouri and Pennsylvania, 1996–1998.MMWR. 1999; 48: 253-256PubMed Google Scholar The correct application of guidelines from the Food and Drug Administration and the American Association of Blood Banks (donors who are residents of non-malarious countries are deferred for one year after return from travel to a malarious area or for three years if they have had malaria, while immigrants from malarious areas are deferred for three years after leaving such areas) can prevent most but not all cases of transfusion-transmitted malaria.12CDC Transfusion-transmitted malaria – Missouri and Pennsylvania, 1996–1998.MMWR. 1999; 48: 253-256PubMed Google Scholar, 13CDC Probable transfusion-transmitted malaria – Houston, Texas 2003.MMWR. 2003; 52: 1075-1076PubMed Google Scholar This patient would have escaped this screening. Is this case exceptional or are “healthy” long-term carriers of P. falciparum infection less rare than one can imagine among semi-immune immigrants? Could rapid tests for Plasmodium antigens and/or PCR help answer this question? We thank Hilde De Bie (Prince Leopold Institute of Tropical Medicine of Antwerp, Belgium) for her microscopic confirmation of the diagnosis. Conflict of interest: No conflict of interest to declare.
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Prédiction distillée sur la base complète
Imitation des enseignantsNi prévalence calibrée, ni vérité terrain. Validation humaine à venir. Apprise à partir de 10 348 étiquettes directes de Codex et de 10 348 étiquettes directes de Gemma. Le mode candidate est l'union des têtes enseignantes seuillées; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont ni des étiquettes humaines ni des étiquettes directes de modèles de pointe.
Scores Codex et Gemma par catégorie
| Catégorie | Codex | Gemma |
|---|---|---|
| Métarecherche | 0,000 | 0,002 |
| Méta-épidémiologie (sens strict) | 0,000 | 0,000 |
| Méta-épidémiologie (sens large) | 0,001 | 0,001 |
| Bibliométrie | 0,001 | 0,000 |
| Études des sciences et des technologies | 0,000 | 0,000 |
| Communication savante | 0,000 | 0,000 |
| Science ouverte | 0,000 | 0,000 |
| Intégrité de la recherche | 0,000 | 0,002 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,001 | 0,000 |
Scores machine (provisoires)
Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.
Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.
score_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découleClassification
machine, non validéePrédiction automatique; un appel candidat d’une seule tête enseignante, pas un consensus.
Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».