ArticleCureus2024
An Interesting Case of Weil's Disease with Diagnostic Challenges.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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0 citing papers in PubMed.
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Weil's disease represents a rare, severe form of leptospirosis, characterized by high mortality risk. The clinical presentation ranges from a self-limited febrile illness to a more severe form of infection where patients may have multiorgan failure. Here we present a case of a young immigrant with abdominal pain, vomiting, and body aches, presenting with mixed hyperbilirubinemia, acute kidney injury (AKI), and moderate thrombocytopenia. Imaging revealed granulomatous pneumonic changes. Despite negative initial studies, the combination of the cholestatic pattern of liver injury, thrombocytopenia, pulmonary and renal involvement, along with recent travel and occupation history, raised concern for leptospirosis. A positive
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