Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Sep;68(3):651-658.
doi: 10.1007/s11686-023-00699-6. Epub 2023 Jul 19.

Albendazole Monotherapy for Pediatric Cystic Echinococcosis: A Case Series

Affiliations

Albendazole Monotherapy for Pediatric Cystic Echinococcosis: A Case Series

Moshe Shmueli et al. Acta Parasitol. 2023 Sep.

Abstract

Background: Data regarding albendazole monotherapy for cystic echinococcosis (CE) are scarce, especially in children. We report our experience treating CE in children with albendazole monotherapy.

Methods: A retrospective case series, 2005-2021, assessing factors leading to albendazole monotherapy, demographic, clinical, duration of treatment and follow-up, and outcome (changes in cyst size and side effects) characteristics.

Results: Overall, we identified 18 patients with 31 cysts; liver: 68% (n = 21), lungs: 29% (n = 9), and kidney: 3% (n = 1). Mean cyst size was 4.5 ± 2.6 cm. Reasons for administrating albendazole monotherapy were small (< 4 cm) cyst size (56%), difficulty to operate (33%) and comorbidity (22%). Duration of treatment (range 1-32 months) was 1, 2-3, 4-6 and > 6 months in 28% (n = 5), 39% (n = 7), 17% (n = 3) and 17% (n = 3) of children, respectively. Duration of follow up (range 1-87 months) was 1, 2-3, 4-6 and > 6 months in 11% (n = 2), 11% (n = 2), 17% (n = 3) and 61% (n = 11) of children, respectively. Overall, 83% (n = 15) of patients experienced lack of cyst growth, and 72% (n = 13) experienced reduction in cyst size, while 44% (n = 8) experienced reduction larger than 50%. Full resolution was noted in 22% (n = 4) of patients. In three cases (17%) treatment failure was recorded: one (6%) recurrence, and two cases (11%) of cyst growth. Neutropenia was recorded in two patients (11%), and liver enzymes elevation was recorded in six patients (33%).

Conclusions: Albendazole monotherapy may be an adequate treatment for selected cases of CE disease in children, especially in CE with small, hepatic cysts.

Keywords: Albendazole; Chemotherapy; Echinococcosis; Hydatid cyst; Pediatrics.

PubMed Disclaimer

References

    1. Thompson RC (2017) Biology and systematics of echinococcus. Adv Parasitol 95:65–109. https://doi.org/10.1016/bs.apar.2016.07.001 - DOI - PubMed
    1. Tamarozzi F, Silva R, Fittipaldo VA, Buonfrate D, Gottstein B, Siles-Lucas M (2021) Serology for the diagnosis of human hepatic cystic echinococcosis and its relation with cyst staging: a systematic review of the literature with meta-analysis. PLoS Negl Trop Dis 15(4):e0009370. https://doi.org/10.1371/journal.pntd.0009370 - DOI - PubMed - PMC
    1. Brunetti E, Kern P, Vuitton DA, Writing Panel for the W-I (2010) Expert consensus for the diagnosis and treatment of cystic and alveolar echinococcosis in humans. Acta Trop 114(1):1–16. https://doi.org/10.1016/j.actatropica.2009.11.001 - DOI - PubMed
    1. Haralabidis S, Diakou A, Frydas S et al (2008) Long-term evaluation of patients with hydatidosis treated with albendazole and praziquantel. Int J Immunopathol Pharmacol 21(2):429–435. https://doi.org/10.1177/039463200802100223 - DOI - PubMed
    1. Yasawy MI, Mohamed AR, Al-Karawi MA (1992) Albendazole in hydatid disease: results in 22 patients. Ann Saudi Med 12(2):152–156. https://doi.org/10.5144/0256-4947.1992.152 - DOI - PubMed

LinkOut - more resources