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Rare Cases of Filarial Chyluria in Children
BACKGROUND: Lymphatic filariasis leading to the passage of white urine or chyle is a rare manifestation in children. Filarial parasite infiltration leading to abnormal lymphatic–urinary communication occurs with prolonged infection. The incubation period ranges from 5 to 20 yrs., thus relatively inf...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8977219/ https://www.ncbi.nlm.nih.gov/pubmed/35386532 http://dx.doi.org/10.2147/IMCRJ.S339207 |
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author | Srivastava, Shetanshu Tiwari, Vandana Sen, Manodeep |
author_facet | Srivastava, Shetanshu Tiwari, Vandana Sen, Manodeep |
author_sort | Srivastava, Shetanshu |
collection | PubMed |
description | BACKGROUND: Lymphatic filariasis leading to the passage of white urine or chyle is a rare manifestation in children. Filarial parasite infiltration leading to abnormal lymphatic–urinary communication occurs with prolonged infection. The incubation period ranges from 5 to 20 yrs., thus relatively infrequent in the pediatric age group. Index of suspicion should be high when a child presents with the passage of white urine because the subclinical manifestation of filarial infection is difficult to recognize. Moreover, more pathognomonic clinical manifestations such as lymphoedema or hydrocoele are present in adulthood. It should also be differentiated from non-parasitic causes like nephrotic syndrome, urates and phosphates in urine, and congenital lymphatic-urinary communication. CASE PRESENTATION: We report two pediatric cases with the intermittent passage of milky white urine since one year. Institutional ethical committee approved the study. In both patients, urine triglycerides were high, and the presence of positive filarial antigen test confirmed the diagnosis. Medical management showed remission of symptoms. Our cases highlight the rare presentation of LF in children and the use of point of care diagnostic tests, management, and outcome in them. CONCLUSION: LF is a rare condition in children, and the index of suspicion should be high for early management. |
format | Online Article Text |
id | pubmed-8977219 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-89772192022-04-05 Rare Cases of Filarial Chyluria in Children Srivastava, Shetanshu Tiwari, Vandana Sen, Manodeep Int Med Case Rep J Case Series BACKGROUND: Lymphatic filariasis leading to the passage of white urine or chyle is a rare manifestation in children. Filarial parasite infiltration leading to abnormal lymphatic–urinary communication occurs with prolonged infection. The incubation period ranges from 5 to 20 yrs., thus relatively infrequent in the pediatric age group. Index of suspicion should be high when a child presents with the passage of white urine because the subclinical manifestation of filarial infection is difficult to recognize. Moreover, more pathognomonic clinical manifestations such as lymphoedema or hydrocoele are present in adulthood. It should also be differentiated from non-parasitic causes like nephrotic syndrome, urates and phosphates in urine, and congenital lymphatic-urinary communication. CASE PRESENTATION: We report two pediatric cases with the intermittent passage of milky white urine since one year. Institutional ethical committee approved the study. In both patients, urine triglycerides were high, and the presence of positive filarial antigen test confirmed the diagnosis. Medical management showed remission of symptoms. Our cases highlight the rare presentation of LF in children and the use of point of care diagnostic tests, management, and outcome in them. CONCLUSION: LF is a rare condition in children, and the index of suspicion should be high for early management. Dove 2022-03-30 /pmc/articles/PMC8977219/ /pubmed/35386532 http://dx.doi.org/10.2147/IMCRJ.S339207 Text en © 2022 Srivastava et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Case Series Srivastava, Shetanshu Tiwari, Vandana Sen, Manodeep Rare Cases of Filarial Chyluria in Children |
title | Rare Cases of Filarial Chyluria in Children |
title_full | Rare Cases of Filarial Chyluria in Children |
title_fullStr | Rare Cases of Filarial Chyluria in Children |
title_full_unstemmed | Rare Cases of Filarial Chyluria in Children |
title_short | Rare Cases of Filarial Chyluria in Children |
title_sort | rare cases of filarial chyluria in children |
topic | Case Series |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8977219/ https://www.ncbi.nlm.nih.gov/pubmed/35386532 http://dx.doi.org/10.2147/IMCRJ.S339207 |
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