| dc.contributor.author | Pathirage, Manoji.M.K | |
| dc.contributor.author | Kularatne, Senanayake.A.M | |
| dc.contributor.author | Weerakoon, Kosala.G | |
| dc.date.accessioned | 2022-12-20T09:14:55Z | |
| dc.date.available | 2022-12-20T09:14:55Z | |
| dc.date.issued | 2019-04-30 | |
| dc.identifier.citation | Journal of Medical Case Reports (2020) | en_US |
| dc.identifier.uri | http://repository.rjt.ac.lk/handle/123456789/5414 | |
| dc.description.abstract | Background: Melioidosis is a potentially fatal bacterial infection caused by Burkholderia pseudomallei. The existence of melioidosis in Sri Lanka was once unheard of, and entertaining it as a diagnosis in clinical practice was extremely rare. Case presentation: In this case report, we describe the clinical, epidemiological, and longitudinal follow-up data of a 58-year-old previously healthy Sinhalese woman who presented to our hospital with protracted febrile illness of 5 weeks’ duration, later developing multiple abscesses at different sites of the body. There was a significant delay in confirming the diagnosis of melioidosis by isolating B. pseudomallei from blood and pus cultures. The patient recovered fully with a prolonged course of antibiotics and has remained in good health over the last 13 years without recurrence. Despite being immunocompetent, she had contracted the infection by a brief contact with mud soil in a footpath. Conclusions: A high index of clinical suspicion along with laboratory support is needed to confirm the diagnosis of melioidosis. Treatment with sensitive antibiotics over a long duration is needed, and longitudinal follow-up is essential to detect recurrences. This case raised awareness and created renewed interest in studies of melioidosis in Sri Lanka. Keywords: Burkholderia pseudomallei, Melioidosis, Sri Lanka | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Springer Nature | en_US |
| dc.subject | Burkholderia pseudomallei, Melioidosis, Sri Lanka | en_US |
| dc.title | Melioidosis after a long silence in Sri Lanka: an environmental hazard and dilemma in diagnosis, with recovery and longitudinal follow-up for 13 years: a case report | en_US |
| dc.type | Article | en_US |