An unusual cause of eosinophilic pleural effusion and migrating biliary stenosis: Strongyloides stercoralis infection in a young immunocompetent man

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Submitted: 5 December 2018
Accepted: 31 January 2019
Published: 20 February 2019
Abstract Views: 1159
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We present the case of a 33-year-old Italian man who came to our attention for epigastralgia associated with polyserositis (pleural, pericardial, and peritoneal effusion with the involvement of the Douglas excavation), in the absence of a significant medical history. Laboratory analysis revealed exudative eosinophilic pleural effusion; serial imaging techniques showed a transient stenosis of the right hepatic duct and a subsequent stenosis of the left hepatic duct. After several negative serological investigations, a positive anti-strongyloides immunoglobulin G antibodies titer rose suspicions of Strongyloides infection, which was confirmed by positive stool sample for parasite. Ivermectin-therapy was started and the patient has fully recovered.

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Paolucci, E., Tonveronachi, E., Praticò, C., Zani, M. C., Paonessa, M. C., Imperatore, M. M. D., & Praticò, B. (2019). An unusual cause of eosinophilic pleural effusion and migrating biliary stenosis: Strongyloides stercoralis infection in a young immunocompetent man. Italian Journal of Medicine, 13(2), 116–120. https://doi.org/10.4081/itjm.2019.1121