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Alveolar echinococcosis in immunocompromised hosts

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CLINICAL MICROBIOLOGY AND INFECTION
卷 29, 期 5, 页码 593-599

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ELSEVIER SCI LTD
DOI: 10.1016/j.cmi.2022.12.010

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Alveolar echinococcosis; Cancer; Echinococcus multilocularis; HIV; Immunosuppressive therapy; Malignant haemopathy; Primary immune de ficiency; Transplantation

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This narrative review examines the presentation of alveolar echinococcosis (AE) in immunocompromised patients and provides recommendations for patient management and future research. The findings indicate a significant association between AE and solid organ transplantation, chronic inflammatory/autoimmune diseases, and malignancies, but not HIV infection. AE in immunocompromised patients is characterized by early diagnosis, atypical imaging, and low sensitivity of serology.
Background: Alveolar echinococcosis (AE) results of an infection with the larval stage of Echinococcus multilocularis. It has been increasingly described in individuals with impaired immune responsiveness. Objectives: This narrative review aims at describing the presentation of AE according to the type of immune impairment, based on retrospective cohorts and case reports. Implications for patient man-agement and future research are proposed accordingly. Sources: Targeted search was conducted in PubMed using ((alveolar echinococcosis) OR (multilocularis)) AND ((immunosuppressive) OR (immunodeficiency) OR (AIDS) OR (solid organ transplant) OR (auto -immunity) OR (immune deficiency)). Only publications in English were considered. Content: Seventeen publications were found, including 13 reports of 55 AE in immunocompromised patients (AE/IS) and 4 retrospective studies of 755 AE immunocompetent patients and 115 AE/IS (13%). The cohorts included 9 (1%) solid organ transplantation (SOT) recipients, 2 (0.2%) HIV patients, 41 (4.7%) with chronic inflammatory/autoimmune diseases (I/AID) and 72 (8.3%) with malignancies. SOT, I/AID and malignancies, but not HIV infection, were significantly associated with AE (odds ratios of 10.8, 1.6, 5.9, and 1.3, respectively). Compared to AE immunocompetent patients, AE/IS was associated with earlier diagnosis (PNM stages I-II: 49/85 (58%) vs. 137/348 (39%), p < 0.001), high rate of atypical imaging (24/ 50 (48%) vs. 106/375 (28%), p < 0.01), and low sensitivity of serology (19/77 (25%) vs. 265/329 (81%), p < 0.001). Unusually extensive or disseminated infections were described in SOT and I/AID patients. Implications: Patients who live in endemic areas should benefit from serology before onset of a long-term immunosuppressive therapy, even if the cost-benefit ratio has to be evaluated. Physicians should explain AE to immunocompromised patients and think about AE when finding a liver lesion. Further research should address gaps in knowledge of AE/IS. Especially, extensive and accurate records of AE cases have to be collected by multinational registries. Brice Autier, Clin Microbiol Infect 2023;29:593 (c) 2022 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

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