Article Text
Statistics from Altmetric.com
Description
A man in his 70s with type 2 diabetes mellitus, chronic kidney disease from diabetic nephropathy with chronic nephrotic-range proteinuria, and no other known medical history presented to the emergency department with a 2-week history of progressive proximal muscular weakness and chronic watery diarrhoea. The results of serial physical examinations demonstrated intact metal status and 3/5 strength in upper and lower extremities bilaterally with 1+ reflexes on presentation which progressed to 1/5 strength with absent reflexes. Laboratory examinations showed a serum creatinine level of 5.0 mg per decilitre (reference range 0.40–1.30) from 3.2 mg per dL 1 month earlier, progressive elevation in creatine kinase up to 16 358 units/L (reference range 11–204), mixed hepatocellular and cholestatic pattern of elevated liver function test abnormalities, and chronically elevated absolute blood eosinophil count to as high as 2.6×1000/μL (reference range 0.0–1.0 × 1000) over the year prior to presentation. Urine microscopy performed as part of the workup for kidney injury revealed many granular casts and a motile larva (video 1) of Strongyloides stercoralis.1 Based on this incidental urine microscopy finding and on the lack of pulmonary symptoms to suggest disseminated disease,2–4 the patient was thought to have a chronic Strongyloides infection and was treated with ivermectin 200 μg/kg for 2 days. Anti-Strongyloides antibody later resulted positive, and additional serological helminthic workup and serial ova and parasite examinations of the stool prior to and after initiation of treatment with ivermectin were negative, though this is known to be a poorly sensitive test.5 Additional workup for progressive weakness, myopathy, and liver function abnormalities was planned, however the patient and his family opted to limit medical interventions to prioritise his comfort and he died of cardiac arrest shortly thereafter.
Learning points
Detection of parasites on urine microscopy is a relatively rare and nearly universally incidental finding, but can be an important first point of discovery of disease in some cases.
Strongyloides stercoralis infection presents a significant diagnostic challenge, with poor sensitivity of the most widely available testing of ova and parasite examination (5%–50%), inability of serological testing to differentiate between prior and active disease states, and the broad scope of possible clinical presentations, particularly in the setting of disseminated disease.
Discovery of S. stercoralis in urine sediment may be a result of urinary specimen contamination from gastrointestinal infection or from urinary tract involvement of infection suggestive of disseminated disease, typically in an immunocompromised host with the vast majority of these patients exhibiting evidence of pulmonary involvement.
Ethics statements
Patient consent for publication
Footnotes
Twitter @meganlebaker, @brewster_ursula
Contributors MLB: writing of the original draft, review and editing. UCB: review and editing.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Case reports provide a valuable learning resource for the scientific community and can indicate areas of interest for future research. They should not be used in isolation to guide treatment choices or public health policy.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.