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Transverse myelitis secondary to Melioidosis; A case report

BACKGROUND: Melioidosis has become an emerging infection in Sri Lanka; a country which is considered non endemic for it. Paraplegia due to Burkholderia pseudomallei is a very rare entity encountered even in countries where the disease is endemic. There are no reported cases of transverse myelitis du...

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Autores principales: Nandasiri, Shanika, Wimalaratna, Harith, Manjula, Muditha, Corea, Enoka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511196/
https://www.ncbi.nlm.nih.gov/pubmed/23020820
http://dx.doi.org/10.1186/1471-2334-12-232
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author Nandasiri, Shanika
Wimalaratna, Harith
Manjula, Muditha
Corea, Enoka
author_facet Nandasiri, Shanika
Wimalaratna, Harith
Manjula, Muditha
Corea, Enoka
author_sort Nandasiri, Shanika
collection PubMed
description BACKGROUND: Melioidosis has become an emerging infection in Sri Lanka; a country which is considered non endemic for it. Paraplegia due to Burkholderia pseudomallei is a very rare entity encountered even in countries where the disease is endemic. There are no reported cases of transverse myelitis due to melioidosis in Sri Lankan population thus we report the first case. CASE PRESENTATION: A 21 year old farmer presented with sudden onset bi lateral lower limb weakness, numbness and urine retention. Examination revealed flaccid areflexic lower limbs with a sensory loss of all modalities and a sensory level at T(10) together with sphincter involvement. MRI of the thoracolumbar spine showed extensive myelitis of the thoracic spine complicating left psoas abscess without definite extension to the spinal cord or cord compression. Burkholderia pseudomallei was isolated from the psoas abscess pus cultures and the diagnosis of melioidosis was confirmed with high titers of Burkholderia pseudomallei antibodies and positive PCR. He was treated with high doses of IV ceftazidime and oral cotrimoxazole for one month with a plan to continue cotrimoxazole and doxycycline till one year. Patient’s general condition improved but the residual neurological problems persisted. CONCLUSION: The exact pathogenesis of spinal cord melioidosis is not quite certain except in the cases where there is direct microbial invasion, which does not appear to be the case in our patient. We postulate our patient’s presentation could be due to ischemia of the spinal cord following septic embolisation or thrombosis of spinal artery due to the abscess nearby. A neurotrophic exotoxin causing myelitis or post infectious immunological demyelination is yet another possibility. This emphasizes the necessity of further studies to elucidate the exact pathogenesis in this type of presentations. Health care professionals in Sri Lanka, where this is an emerging infection, need to improve their knowledge regarding this disease and should have high degree of suspicion to make a correct and a timely diagnosis to reduce the morbidity and mortality due to Burkholderia pseudomallei infection. It is highly likely that this infection is under diagnosed in developing countries where diagnostic facilities are minimal. Therefore strategies to improve the awareness and upgrade the diagnostic facilities need to be implemented in near future.
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spelling pubmed-35111962012-12-01 Transverse myelitis secondary to Melioidosis; A case report Nandasiri, Shanika Wimalaratna, Harith Manjula, Muditha Corea, Enoka BMC Infect Dis Case Report BACKGROUND: Melioidosis has become an emerging infection in Sri Lanka; a country which is considered non endemic for it. Paraplegia due to Burkholderia pseudomallei is a very rare entity encountered even in countries where the disease is endemic. There are no reported cases of transverse myelitis due to melioidosis in Sri Lankan population thus we report the first case. CASE PRESENTATION: A 21 year old farmer presented with sudden onset bi lateral lower limb weakness, numbness and urine retention. Examination revealed flaccid areflexic lower limbs with a sensory loss of all modalities and a sensory level at T(10) together with sphincter involvement. MRI of the thoracolumbar spine showed extensive myelitis of the thoracic spine complicating left psoas abscess without definite extension to the spinal cord or cord compression. Burkholderia pseudomallei was isolated from the psoas abscess pus cultures and the diagnosis of melioidosis was confirmed with high titers of Burkholderia pseudomallei antibodies and positive PCR. He was treated with high doses of IV ceftazidime and oral cotrimoxazole for one month with a plan to continue cotrimoxazole and doxycycline till one year. Patient’s general condition improved but the residual neurological problems persisted. CONCLUSION: The exact pathogenesis of spinal cord melioidosis is not quite certain except in the cases where there is direct microbial invasion, which does not appear to be the case in our patient. We postulate our patient’s presentation could be due to ischemia of the spinal cord following septic embolisation or thrombosis of spinal artery due to the abscess nearby. A neurotrophic exotoxin causing myelitis or post infectious immunological demyelination is yet another possibility. This emphasizes the necessity of further studies to elucidate the exact pathogenesis in this type of presentations. Health care professionals in Sri Lanka, where this is an emerging infection, need to improve their knowledge regarding this disease and should have high degree of suspicion to make a correct and a timely diagnosis to reduce the morbidity and mortality due to Burkholderia pseudomallei infection. It is highly likely that this infection is under diagnosed in developing countries where diagnostic facilities are minimal. Therefore strategies to improve the awareness and upgrade the diagnostic facilities need to be implemented in near future. BioMed Central 2012-09-28 /pmc/articles/PMC3511196/ /pubmed/23020820 http://dx.doi.org/10.1186/1471-2334-12-232 Text en Copyright ©2012 Nandasiri et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Nandasiri, Shanika
Wimalaratna, Harith
Manjula, Muditha
Corea, Enoka
Transverse myelitis secondary to Melioidosis; A case report
title Transverse myelitis secondary to Melioidosis; A case report
title_full Transverse myelitis secondary to Melioidosis; A case report
title_fullStr Transverse myelitis secondary to Melioidosis; A case report
title_full_unstemmed Transverse myelitis secondary to Melioidosis; A case report
title_short Transverse myelitis secondary to Melioidosis; A case report
title_sort transverse myelitis secondary to melioidosis; a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511196/
https://www.ncbi.nlm.nih.gov/pubmed/23020820
http://dx.doi.org/10.1186/1471-2334-12-232
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