Evidence map›Paper›PMID 41229647›Full record

ArticleEuropean journal of case reports in internal medicine2025

West Nile Virus Neuroinvasive Disease Presenting with Acquired Fanconi Syndrome, Which Resolved on Recovery.

Paraskevi Karamani, Giorgos Souroullas, Amare Negash, Thomas Tavos, George Miltiadous, Haralampos Milionis

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Article in European journal of case reports in internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Paraskevi KaramaniDepartment of Internal Medicine, Apollonion Private Hospital, Nicosia, Cyprus.
Giorgos SouroullasDepartment of Internal Medicine, Apollonion Private Hospital, Nicosia, Cyprus.
Amare NegashDepartment of Internal Medicine, Apollonion Private Hospital, Nicosia, Cyprus.
Thomas TavosDepartment of Internal Medicine, Apollonion Private Hospital, Nicosia, Cyprus.
George MiltiadousDepartment of Internal Medicine, Apollonion Private Hospital, Nicosia, Cyprus.
Haralampos MilionisDepartment of Internal Medicine, School of Medicine, University of Ioannina, Ioannina, Greece.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: West Nile virus (WNV) is a mosquito-borne flavivirus that can cause neuroinvasive disease. Renal involvement is uncommon and acquired Fanconi syndrome has not been previously described in association with WNV. Case presentation: An 81-year-old male from Cyprus presented with fever, headache, disorientation, and signs of meningoencephalitis. Cerebrospinal fluid (CSF) analysis and neuroimaging supported the diagnosis of viral encephalitis. Extensive microbiological testing revealed WNV ribonucleic acid in urine and blood, but not in the CSF. The patient developed persistent hypokalaemia, metabolic acidosis, hypomagnesemia, and hypouricemia, with elevated fractional excretion of these solutes-findings consistent with Fanconi syndrome. Acyclovir was discontinued, and supportive treatment was provided. Renal function and electrolyte levels normalized by day 9. At 2-month follow-up, the patient had fully recovered with normal renal parameters. Conclusion: Renal complications of WNV are rarely documented and this case of WNV associated acquired Fanconi syndrome underscores the importance of evaluating kidney function and electrolyte status in WNV-infected patients. Early recognition of tubular dysfunction may prevent complications and improve outcomes. LEARNING POINTS: While renal complications of West Nile virus (WNV) are documented in rare cases, this is the first reported case of WNV-associated Fanconi syndrome.

Indexed as

Fanconi’s syndromehypokalaemiaproximal tubular dysfunctionWest Nile virus

Identifiers

PMID41229647
PMCPMC12604865

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