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A Rare Case of Weil’s Syndrome With Extreme Hyperbilirubinemia in an Urban Setting
We present a unique case of Weil’s disease, a severe form of leptospirosis caused by Leptospira interrogans, a rare agent seen in both temperate and tropical climates but is more commonly seen in tropical climates and transmitted to humans commonly by rodent urine contamination. It is an under-repor...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10105601/ https://www.ncbi.nlm.nih.gov/pubmed/37069885 http://dx.doi.org/10.7759/cureus.36243 |
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author | Ansari, Nida Bhargava, Rhea Elagami, Mohamed M Gashi, Taulant Perez, Carlos Suh, Jin Baddoura, Walid |
author_facet | Ansari, Nida Bhargava, Rhea Elagami, Mohamed M Gashi, Taulant Perez, Carlos Suh, Jin Baddoura, Walid |
author_sort | Ansari, Nida |
collection | PubMed |
description | We present a unique case of Weil’s disease, a severe form of leptospirosis caused by Leptospira interrogans, a rare agent seen in both temperate and tropical climates but is more commonly seen in tropical climates and transmitted to humans commonly by rodent urine contamination. It is an under-reported infection, with 1.03 million cases documented annually, and is not commonly found in the United States. A 32-year-old African American male presented with abdominal pain and pressure in his chest associated with nausea, vomiting, and diarrhea. On exam, scleral icterus, sublingual jaundice, and hepatosplenomegaly were noted. Imaging studies revealed the patient had incidental situs inversus and dextrocardia. Labs revealed leukocytosis, thrombocytopenia, transaminitis, and significant direct hyperbilirubinemia of over 30 mg/dL. An extensive workup revealed the patient had leptospirosis due to rat contamination in his apartment. The patient was treated with doxycycline, and his clinical status improved. The heterogeneous and unique clinical presentation of leptospirosis gives rise to a broad differential diagnosis. We aim to encourage physicians who encounter similar presentations in similar urban settings in the United States to include leptospirosis in their differential. |
format | Online Article Text |
id | pubmed-10105601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-101056012023-04-16 A Rare Case of Weil’s Syndrome With Extreme Hyperbilirubinemia in an Urban Setting Ansari, Nida Bhargava, Rhea Elagami, Mohamed M Gashi, Taulant Perez, Carlos Suh, Jin Baddoura, Walid Cureus Gastroenterology We present a unique case of Weil’s disease, a severe form of leptospirosis caused by Leptospira interrogans, a rare agent seen in both temperate and tropical climates but is more commonly seen in tropical climates and transmitted to humans commonly by rodent urine contamination. It is an under-reported infection, with 1.03 million cases documented annually, and is not commonly found in the United States. A 32-year-old African American male presented with abdominal pain and pressure in his chest associated with nausea, vomiting, and diarrhea. On exam, scleral icterus, sublingual jaundice, and hepatosplenomegaly were noted. Imaging studies revealed the patient had incidental situs inversus and dextrocardia. Labs revealed leukocytosis, thrombocytopenia, transaminitis, and significant direct hyperbilirubinemia of over 30 mg/dL. An extensive workup revealed the patient had leptospirosis due to rat contamination in his apartment. The patient was treated with doxycycline, and his clinical status improved. The heterogeneous and unique clinical presentation of leptospirosis gives rise to a broad differential diagnosis. We aim to encourage physicians who encounter similar presentations in similar urban settings in the United States to include leptospirosis in their differential. Cureus 2023-03-16 /pmc/articles/PMC10105601/ /pubmed/37069885 http://dx.doi.org/10.7759/cureus.36243 Text en Copyright © 2023, Ansari et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Gastroenterology Ansari, Nida Bhargava, Rhea Elagami, Mohamed M Gashi, Taulant Perez, Carlos Suh, Jin Baddoura, Walid A Rare Case of Weil’s Syndrome With Extreme Hyperbilirubinemia in an Urban Setting |
title | A Rare Case of Weil’s Syndrome With Extreme Hyperbilirubinemia in an Urban Setting |
title_full | A Rare Case of Weil’s Syndrome With Extreme Hyperbilirubinemia in an Urban Setting |
title_fullStr | A Rare Case of Weil’s Syndrome With Extreme Hyperbilirubinemia in an Urban Setting |
title_full_unstemmed | A Rare Case of Weil’s Syndrome With Extreme Hyperbilirubinemia in an Urban Setting |
title_short | A Rare Case of Weil’s Syndrome With Extreme Hyperbilirubinemia in an Urban Setting |
title_sort | rare case of weil’s syndrome with extreme hyperbilirubinemia in an urban setting |
topic | Gastroenterology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10105601/ https://www.ncbi.nlm.nih.gov/pubmed/37069885 http://dx.doi.org/10.7759/cureus.36243 |
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