Lassina Sere, Thierry K Guiguemde, Fabienne Sanou, Arielle Belem, Nadine Ouedraogo, Bertille Ouedraogo, Marcel P Sawadogo, Achille Aouba
{"title":"[Myelitis Associated with Visceral Leishmaniasis Due to Leishmania infantum in Burkina Faso: A Case Report].","authors":"Lassina Sere, Thierry K Guiguemde, Fabienne Sanou, Arielle Belem, Nadine Ouedraogo, Bertille Ouedraogo, Marcel P Sawadogo, Achille Aouba","doi":"10.1016/j.revmed.2026.09.006","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Visceral leishmaniasis with Leishmania infantum (VL/LI) remains unreported in West Africa. We describe here an unprecedented autochthonous case of VL/LI in Burkina Faso, associated with myelitis.</p><p><strong>Case report: </strong>A teenage girl was hospitalized for prolonged fever, flaccid paraplegia, severe pancytopenia, hepatosplenomegaly, and immobilization-related pulmonary embolism with pleural effusion. Immunological, hematological, and microbiological investigations, including tuberculosis, particularly on pleural, bone marrow fluids, and salivary gland biopsy were non-diagnostic. Spinal MRI revealed thoracic myelitis. Empirical anti-tuberculous and immunosuppressive drugs for sarcoidosis (methylprednisolone/adalimumab) were ineffective and favoured ulcero-necrotic cutaneous nodules emergence, prompting VL diagnostic, confirmed by LI PCR positivity on cutaneous and blood samples.</p><p><strong>Conclusion: </strong>Although VL/LI is reported in local domestic dogs, this case provides the first documentation of human VL/LI in West Africa, endemic region for L. major, associated with a probable specific myelitis. This case is reminiscent of the exceptional involvements of central nervous system in the clinical spectrum of VL.</p>","PeriodicalId":94122,"journal":{"name":"La Revue de medecine interne","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2026-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"La Revue de medecine interne","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.revmed.2026.09.006","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Visceral leishmaniasis with Leishmania infantum (VL/LI) remains unreported in West Africa. We describe here an unprecedented autochthonous case of VL/LI in Burkina Faso, associated with myelitis.
Case report: A teenage girl was hospitalized for prolonged fever, flaccid paraplegia, severe pancytopenia, hepatosplenomegaly, and immobilization-related pulmonary embolism with pleural effusion. Immunological, hematological, and microbiological investigations, including tuberculosis, particularly on pleural, bone marrow fluids, and salivary gland biopsy were non-diagnostic. Spinal MRI revealed thoracic myelitis. Empirical anti-tuberculous and immunosuppressive drugs for sarcoidosis (methylprednisolone/adalimumab) were ineffective and favoured ulcero-necrotic cutaneous nodules emergence, prompting VL diagnostic, confirmed by LI PCR positivity on cutaneous and blood samples.
Conclusion: Although VL/LI is reported in local domestic dogs, this case provides the first documentation of human VL/LI in West Africa, endemic region for L. major, associated with a probable specific myelitis. This case is reminiscent of the exceptional involvements of central nervous system in the clinical spectrum of VL.