17 research outputs found

    Neurocysticercosis, re-infection or inflammation?

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    International audienc

    Histological and molecular biology diagnosis of neurocysticercosis in a patient without history of travel to endemic areas – Case report

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    Background: in endemic areas, neurocysticercosis appears mainly as a single, large, spherical and non-enhancing intracranial cyst. Case presentation: an atypical case of neurocysticercosis (NCC) in a French Caucasian, without history of travel to endemic areas, was confirmed by histology and molecular speciation. Imaging was atypical, showing several hook-bearing scolices visible in the cyst, while the serology employed was non-contributary. Conclusions: NCC should be considered when multiple taeniid scolices are observed within the same cystic lesion

    Toxoplasmose pendant la grossesse : proposition actuelle de prise en charge pratique

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    International audienceThe burden of congenital toxoplasmosis has become small in France today, in particular as a result of timely therapy for pregnant women, fetuses and newborns. Thus, the French screening and prevention program has been evaluated and recently confirmed despite a decline over time in the incidence of toxoplasmosis. Serological diagnosis of maternal seroconversion is usually simple but can be difficult when the first trimester test shows the presence of IgM, requiring referral to an expert laboratory. Woman with confirmed seroconversion should be referred quickly to an expert center, which will decide with her on treatment and antenatal diagnosis. Although the level of proof is moderate, there is a body of evidence in favor of active prophylactic prenatal treatment started as early as possible (ideally within 3 weeks of seroconversion) to reduce the risk of maternal-fetal transmission, as well as symptoms in children. The recommended therapies to prevent maternal-fetal transmission are: (1) spiramycin in case of maternal infection before 14 gestational weeks; (2) pyrimethamine and sulfadiazine (P-S) with folinic acid in case of maternal infection at 14 WG or more. Amniocentesis is recommended to guide prenatal and neonatal care. If fetal infection is diagnosed by PCR on amniotic fluid, therapy with P-S should be initiated as early as possible or continued in order reduce the risk of damage to the brain or eyes. Further research is required to validate new approaches to preventing congenital toxoplasmosis

    Prise en charge de la toxoplasmose oculaire en France : résultats d’une étude Delphi modifiée

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    International audienceOBJECTIVE: To evaluate diagnostic and therapeutic practices and then establish a consensus on the management of ocular toxoplasmosis in France through a Delphi study. MATERIALS AND METHODS: Twenty-three French experts in ocular toxoplasmosis were invited to respond to a modified Delphi study conducted online, in the form of two questionnaires, in an attempt to establish a consensus on the diagnosis and management of this pathology. The threshold for identical responses to reach consensus was set at 70 %. RESULTS: The responses of 19 experts out of the 23 selected were obtained on the first questionnaire and 16 experts on the second. The main elements agreed upon by the experts were to treat patients with a decrease in visual acuity or an infectious focus within the posterior pole, to treat peripheral lesions only in the presence of significant inflammation, the prescription of first-line treatment with pyrimethamine-azithromycin, the use of corticosteroid therapy after a period of 24 to 48hours, the prophylaxis of frequent recurrences (more than 2 episodes per year) with trimethoprim-sulfamethoxazole as well as the implementation of prophylactic treatment of recurrences in immunocompromised patients. On the other hand, no consensus emerged with regard to the examinations to be carried out for the etiological diagnosis (anterior chamber paracentesis, fluorescein angiography, serology, etc.), second-line treatment (in the case of failure of first-line treatment), or treatment of peripheral foci. CONCLUSION: This study lays the foundations for possible randomized scientific studies to be conducted to clarify the management of ocular toxoplasmosis, on the one hand to confirm consensual clinical practices and on the other hand to guide practices for which no formal consensus has been demonstrated.RésuméObjectifÉvaluer les pratiques diagnostiques et thérapeutiques puis établir un consensus sur la prise en charge de la toxoplasmose oculaire en France grâce à une étude Delphi.MéthodesVingt-trois experts français de la toxoplasmose oculaire ont été invités à répondre à une étude Delphi modifiée menée en ligne, sous forme de deux questionnaires, afin de tenter d’établir un consensus sur le diagnostic et la prise en charge de cette pathologie. Le seuil de réponses identiques pour aboutir à un consensus a été fixé à 70 %.RésultatsLes réponses de 19 experts sur les 23 sélectionnés ont été obtenues au premier questionnaire et de 16 experts au second. Les principaux éléments qui font consensus auprès des experts sont de traiter les patients avec une baisse d’acuité visuelle ou un foyer infectieux au pôle postérieur, l’instauration d’un traitement face à un foyer périphérique seulement en cas d’inflammation importante, la prescription d’un traitement de première intention par l’association pyriméthamine–azithromycine, l’utilisation d’un traitement par corticostéroïdes après un délai de 24 à 48 h, la prophylaxie des récidives fréquentes (plus de 2 épisodes par an) par triméthoprime-sulfaméthoxazole ainsi que la mise en place d’un traitement prophylactique des récidives chez les patients immunodéprimés. En revanche, aucun consensus ne se dégage pour les examens à réaliser pour le diagnostic étiologique (ponction de chambre antérieure, angiographie à la fluorescéine, sérologie…), pour les traitements de seconde intention (en cas d’échec du traitement de première ligne) ni pour le traitement des foyers périphériques.ConclusionLa présente étude pose les bases d’éventuelles études scientifiques randomisées à mener afin de clarifier les prises en charge la toxoplasmose oculaire, d’une part pour confirmer les habitudes cliniques qui font consensus, d’autre part pour guider les pratiques pour lesquelles aucun consensus formel n’est mis en évidence
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