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A Rare Presentation of Leptospirosis

Leptospirosis has a wide spectrum of clinical manifestations. Acute renal failure, an important complication, generally involves interstitial and tubular damage. We describe the case of a 42-year-old man who was admitted with fever, back pain and periorbital oedema. He had hypertension, thrombocytop...

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Detalles Bibliográficos
Autores principales: Silva, Filipa, Brandão, Mariana, Esteves, Afonso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SMC Media Srl 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346843/
https://www.ncbi.nlm.nih.gov/pubmed/30755889
http://dx.doi.org/10.12890/2016_000447
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author Silva, Filipa
Brandão, Mariana
Esteves, Afonso
author_facet Silva, Filipa
Brandão, Mariana
Esteves, Afonso
author_sort Silva, Filipa
collection PubMed
description Leptospirosis has a wide spectrum of clinical manifestations. Acute renal failure, an important complication, generally involves interstitial and tubular damage. We describe the case of a 42-year-old man who was admitted with fever, back pain and periorbital oedema. He had hypertension, thrombocytopenia, acute renal failure, hypoalbuminaemia, hypertriglyceridaemia and proteinuria >4.00 g/l. The renal biopsy showed mesangioproliferative glomerulonephritis. Due to the epidemiological context and clinical picture, ceftriaxone was started with rapid clinical improvement. Blood PCR for leptospira came back positive. The presentation of leptospirosis as nephrotic syndrome is rare and this diagnosis should be considered before performing a renal biopsy. LEARNING POINTS: Leptospirosis is a zoonosis with a wide spectrum of clinical manifestations including acute renal failure, which is an important complication. Leptospirosis should be considered in a patient with nephrotic syndrome and acute renal failure if the epidemiological context is favourable. Leptospirosis is one of the causes of nephrotic syndrome where a renal biopsy is not indicated.
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spelling pubmed-63468432019-02-12 A Rare Presentation of Leptospirosis Silva, Filipa Brandão, Mariana Esteves, Afonso Eur J Case Rep Intern Med Articles Leptospirosis has a wide spectrum of clinical manifestations. Acute renal failure, an important complication, generally involves interstitial and tubular damage. We describe the case of a 42-year-old man who was admitted with fever, back pain and periorbital oedema. He had hypertension, thrombocytopenia, acute renal failure, hypoalbuminaemia, hypertriglyceridaemia and proteinuria >4.00 g/l. The renal biopsy showed mesangioproliferative glomerulonephritis. Due to the epidemiological context and clinical picture, ceftriaxone was started with rapid clinical improvement. Blood PCR for leptospira came back positive. The presentation of leptospirosis as nephrotic syndrome is rare and this diagnosis should be considered before performing a renal biopsy. LEARNING POINTS: Leptospirosis is a zoonosis with a wide spectrum of clinical manifestations including acute renal failure, which is an important complication. Leptospirosis should be considered in a patient with nephrotic syndrome and acute renal failure if the epidemiological context is favourable. Leptospirosis is one of the causes of nephrotic syndrome where a renal biopsy is not indicated. SMC Media Srl 2016-08-26 /pmc/articles/PMC6346843/ /pubmed/30755889 http://dx.doi.org/10.12890/2016_000447 Text en © EFIM 2016 This article is licensed under a Commons Attribution Non-Commercial 4.0 License (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Articles
Silva, Filipa
Brandão, Mariana
Esteves, Afonso
A Rare Presentation of Leptospirosis
title A Rare Presentation of Leptospirosis
title_full A Rare Presentation of Leptospirosis
title_fullStr A Rare Presentation of Leptospirosis
title_full_unstemmed A Rare Presentation of Leptospirosis
title_short A Rare Presentation of Leptospirosis
title_sort rare presentation of leptospirosis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346843/
https://www.ncbi.nlm.nih.gov/pubmed/30755889
http://dx.doi.org/10.12890/2016_000447
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