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DOI 10.1186/s13256-021-02978-0

Медицинская библиотека · Journal of medical case reports · 2021

Acute kidney injury with partial Fanconi syndrome in a patient with leptospirosis: a case report.

Weiner Marc, Coen Matteo, Serratrice Jacques, Mavrakanas Thomas A, Leidi Antonio

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Аннотация

BACKGROUND

Leptospirosis is an underdiagnosed bacterial infection with nonspecific symptoms, hence, a diagnostic challenge. Identifying a case of leptospirosis in Switzerland is uncommon. Although kidney complications are frequent in severe forms, including tubular dysfunction, observing this complication is rare in our country. We report the case of a patient with leptospirosis and kidney dysfunction, which was notable for proximal tubulopathy. This case report describes the diagnosis and management of this patient's tubular dysfunction.

CASE PRESENTATION: A 34-year-old Caucasian male known for alcohol and drug abuse presented to our emergency department suffering from severe pain in the lower limbs, jaundice, and fever with flu-like symptoms. Physical examination was not contributory. Blood tests showed cytopenia, elevated inflammatory markers, acute kidney injury, and altered liver function tests with predominant cholestasis. Urinalysis showed proteinuria and significant glycosuria without concomitant hyperglycemia. Leptospirosis was suspected and confirmed by both positive serum polymerase chain reaction and elevated immunoglobulin M for Leptospira interrogans. The patient was treated with intravenous amoxicillin-clavulanate and doxycycline for 7 days. After antibiotic treatment, symptoms disappeared, and kidney dysfunction completely resolved.

CONCLUSION

Our case focuses on the description of leptospirosis-related acute kidney injury with proximal tubular dysfunction, which is a rare finding in Switzerland.

Для цитирования: Weiner Marc, Coen Matteo, Serratrice Jacques, Mavrakanas Thomas A, Leidi Antonio. Acute kidney injury with partial Fanconi syndrome in a patient with leptospirosis: a case report.. Journal of medical case reports. 2021. DOI: 10.1186/s13256-021-02978-0.

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