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Severe mucosal leishmaniasis with torpid and fatal evolution

Mucosal leishmaniasis is a clinical condition that is difficult to diagnose and treat and usually precedes a cutaneous leishmaniasis condition with a long latency period as observed in our study of a patient who experienced a torpid evolution in 9 months, caused by having had cutaneous leishmaniasis...

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Autor principal: Jaimes, Jesús Rojas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376139/
https://www.ncbi.nlm.nih.gov/pubmed/35990382
http://dx.doi.org/10.1002/ccr3.6220
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author Jaimes, Jesús Rojas
author_facet Jaimes, Jesús Rojas
author_sort Jaimes, Jesús Rojas
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description Mucosal leishmaniasis is a clinical condition that is difficult to diagnose and treat and usually precedes a cutaneous leishmaniasis condition with a long latency period as observed in our study of a patient who experienced a torpid evolution in 9 months, caused by having had cutaneous leishmaniasis on the neck without therapeutic treatment, although with ulcer closure 18 years earlier, incomplete treatment with antimonials and amphotericin B, with the destruction of the eyeball, a large area of necrosis on the face and nasal bone exposure. Additionally, the patient had chronic anemia (9.4 g/dl), lymphopenia and neutrophilia (lymphocytes 13.1%, neutrophils 84.4%), and co‐infections by fungi (yeasts and hyphae) and Gram‐negative bacteria (multidrug‐resistant Proteus mirabilis and Escherichia coli) leading to sepsis and subsequent death of the patient.
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spelling pubmed-93761392022-08-18 Severe mucosal leishmaniasis with torpid and fatal evolution Jaimes, Jesús Rojas Clin Case Rep Case Report Mucosal leishmaniasis is a clinical condition that is difficult to diagnose and treat and usually precedes a cutaneous leishmaniasis condition with a long latency period as observed in our study of a patient who experienced a torpid evolution in 9 months, caused by having had cutaneous leishmaniasis on the neck without therapeutic treatment, although with ulcer closure 18 years earlier, incomplete treatment with antimonials and amphotericin B, with the destruction of the eyeball, a large area of necrosis on the face and nasal bone exposure. Additionally, the patient had chronic anemia (9.4 g/dl), lymphopenia and neutrophilia (lymphocytes 13.1%, neutrophils 84.4%), and co‐infections by fungi (yeasts and hyphae) and Gram‐negative bacteria (multidrug‐resistant Proteus mirabilis and Escherichia coli) leading to sepsis and subsequent death of the patient. John Wiley and Sons Inc. 2022-08-14 /pmc/articles/PMC9376139/ /pubmed/35990382 http://dx.doi.org/10.1002/ccr3.6220 Text en © 2022 The Author. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Report
Jaimes, Jesús Rojas
Severe mucosal leishmaniasis with torpid and fatal evolution
title Severe mucosal leishmaniasis with torpid and fatal evolution
title_full Severe mucosal leishmaniasis with torpid and fatal evolution
title_fullStr Severe mucosal leishmaniasis with torpid and fatal evolution
title_full_unstemmed Severe mucosal leishmaniasis with torpid and fatal evolution
title_short Severe mucosal leishmaniasis with torpid and fatal evolution
title_sort severe mucosal leishmaniasis with torpid and fatal evolution
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376139/
https://www.ncbi.nlm.nih.gov/pubmed/35990382
http://dx.doi.org/10.1002/ccr3.6220
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