| Literature DB >> 32087332 |
Kathrin Rothe1, Juri Katchanov2, Jochen Schneider2, Christoph D Spinner2, Veit Phillip2, Dirk H Busch3, Dennis Tappe4, Rickmer Braren5, Roland M Schmid2, Julia Slotta-Huspenina6.
Abstract
We report a case of a fatal Strongyloides stercoralis hyperinfection syndrome (SHS) in a migrant from Kenya, who had been living in Germany for three decades. A short-course oral steroid treatment for Chronic Obstructive Pulmonary Disease (COPD) exacerbation had been administered four weeks prior to the presentation. The initial clinical and radiological findings suggested a mechanical small bowel obstruction as a cause of ileus. Our case highlights the importance of maintaining a high index of suspicion for strongyloidiasis in patients from endemic areas even years after they left the country of origin. It demonstrates that even a five-day course of prednisolone is able to trigger SHS in patients with underlying strongyloidiasis. History of frequent previous administration of oral prednisolone for COPD exacerbations in our case raises the question why and how the last steroid regimen provoked SHS. SHS can present with multiple gastrointestinal symptoms including ileus and the absence of eosinophilia during the whole course of the disease should not lower the level of suspicion in the appropriate clinical setting.Entities:
Keywords: Corticosteroids; Helminths; Hyperinfection syndrome; Strongyloides stercoralis; Strongyloidiasis
Year: 2020 PMID: 32087332 DOI: 10.1016/j.parint.2020.102087
Source DB: PubMed Journal: Parasitol Int ISSN: 1383-5769 Impact factor: 2.230