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Two cases of fungal cyst infection in ADPKD: is this really a rare complication?
BACKGROUND: Cyst infection is a prevalent complication in autosomal dominant polycystic kidney disease (ADPKD) patients, however therapeutic and diagnostic approaches towards this condition remain unclear. The confirmation of a likely episode of cyst infection by isolating the pathogenic microorgani...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819534/ https://www.ncbi.nlm.nih.gov/pubmed/31664917 http://dx.doi.org/10.1186/s12879-019-4444-y |
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author | Onuchic, Laura Sato, Victor Augusto Hamamoto de Menezes Neves, Precil Diego Miranda Balbo, Bruno Eduardo Pedroso Portela-Neto, Antônio Abel Ferreira, Fernanda Trani Watanabe, Elieser Hitoshi Watanabe, Andreia de Almeida, Maria Cláudia Stockler de Abreu Testagrossa, Leonardo Chocair, Pedro Renato Onuchic, Luiz Fernando |
author_facet | Onuchic, Laura Sato, Victor Augusto Hamamoto de Menezes Neves, Precil Diego Miranda Balbo, Bruno Eduardo Pedroso Portela-Neto, Antônio Abel Ferreira, Fernanda Trani Watanabe, Elieser Hitoshi Watanabe, Andreia de Almeida, Maria Cláudia Stockler de Abreu Testagrossa, Leonardo Chocair, Pedro Renato Onuchic, Luiz Fernando |
author_sort | Onuchic, Laura |
collection | PubMed |
description | BACKGROUND: Cyst infection is a prevalent complication in autosomal dominant polycystic kidney disease (ADPKD) patients, however therapeutic and diagnostic approaches towards this condition remain unclear. The confirmation of a likely episode of cyst infection by isolating the pathogenic microorganism in a clinical scenario is possible only in the minority of cases. The available antimicrobial treatment guidelines, therefore, might not be appropriate to some patients. CASE PRESENTATION: We describe two unique cases of kidney cyst infection by Candida albicans, a condition that has not been previously described in literature. Both cases presented clear risk factors for Candida spp. infection. However, since there was no initial indication of cyst aspiration and culture, antifungal therapy was not immediately started and empirical treatment was initiated as recommended by the current guidelines. Antifungal treatment was instituted in both cases along the clinical course, according to their specificities. CONCLUSION: Our report highlights the possibility of Candida spp. cyst infection. Failure of clinical improvement with antibiotics should raise the suspicion of a fungal infection. Identification of infected cysts should be pursued in such cases, particularly with PET-CT, and when technically possible followed by cyst aspiration and culture to guide treatment. Risk factors for this condition, such as Candida spp. colonization, previous antimicrobial therapy, hemodialysis, necrotizing pancreatitis, gastrointestinal/hepatobiliary surgical procedure, central venous catheter, total parenteral nutrition, diabetes mellitus and immunodeficiency (neutropenia < 500 neutrophils/mL, hematologic malignancy, chemotherapy, immunosuppressant drugs), should be also considered accepted criteria for empirical antifungal therapy. |
format | Online Article Text |
id | pubmed-6819534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68195342019-10-31 Two cases of fungal cyst infection in ADPKD: is this really a rare complication? Onuchic, Laura Sato, Victor Augusto Hamamoto de Menezes Neves, Precil Diego Miranda Balbo, Bruno Eduardo Pedroso Portela-Neto, Antônio Abel Ferreira, Fernanda Trani Watanabe, Elieser Hitoshi Watanabe, Andreia de Almeida, Maria Cláudia Stockler de Abreu Testagrossa, Leonardo Chocair, Pedro Renato Onuchic, Luiz Fernando BMC Infect Dis Case Report BACKGROUND: Cyst infection is a prevalent complication in autosomal dominant polycystic kidney disease (ADPKD) patients, however therapeutic and diagnostic approaches towards this condition remain unclear. The confirmation of a likely episode of cyst infection by isolating the pathogenic microorganism in a clinical scenario is possible only in the minority of cases. The available antimicrobial treatment guidelines, therefore, might not be appropriate to some patients. CASE PRESENTATION: We describe two unique cases of kidney cyst infection by Candida albicans, a condition that has not been previously described in literature. Both cases presented clear risk factors for Candida spp. infection. However, since there was no initial indication of cyst aspiration and culture, antifungal therapy was not immediately started and empirical treatment was initiated as recommended by the current guidelines. Antifungal treatment was instituted in both cases along the clinical course, according to their specificities. CONCLUSION: Our report highlights the possibility of Candida spp. cyst infection. Failure of clinical improvement with antibiotics should raise the suspicion of a fungal infection. Identification of infected cysts should be pursued in such cases, particularly with PET-CT, and when technically possible followed by cyst aspiration and culture to guide treatment. Risk factors for this condition, such as Candida spp. colonization, previous antimicrobial therapy, hemodialysis, necrotizing pancreatitis, gastrointestinal/hepatobiliary surgical procedure, central venous catheter, total parenteral nutrition, diabetes mellitus and immunodeficiency (neutropenia < 500 neutrophils/mL, hematologic malignancy, chemotherapy, immunosuppressant drugs), should be also considered accepted criteria for empirical antifungal therapy. BioMed Central 2019-10-29 /pmc/articles/PMC6819534/ /pubmed/31664917 http://dx.doi.org/10.1186/s12879-019-4444-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Onuchic, Laura Sato, Victor Augusto Hamamoto de Menezes Neves, Precil Diego Miranda Balbo, Bruno Eduardo Pedroso Portela-Neto, Antônio Abel Ferreira, Fernanda Trani Watanabe, Elieser Hitoshi Watanabe, Andreia de Almeida, Maria Cláudia Stockler de Abreu Testagrossa, Leonardo Chocair, Pedro Renato Onuchic, Luiz Fernando Two cases of fungal cyst infection in ADPKD: is this really a rare complication? |
title | Two cases of fungal cyst infection in ADPKD: is this really a rare complication? |
title_full | Two cases of fungal cyst infection in ADPKD: is this really a rare complication? |
title_fullStr | Two cases of fungal cyst infection in ADPKD: is this really a rare complication? |
title_full_unstemmed | Two cases of fungal cyst infection in ADPKD: is this really a rare complication? |
title_short | Two cases of fungal cyst infection in ADPKD: is this really a rare complication? |
title_sort | two cases of fungal cyst infection in adpkd: is this really a rare complication? |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819534/ https://www.ncbi.nlm.nih.gov/pubmed/31664917 http://dx.doi.org/10.1186/s12879-019-4444-y |
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