Skip to main content
Top
Published in: BMC Infectious Diseases 1/2018

Open Access 01-12-2018 | Case report

Relapse of chronic melioidosis in a paediatric cystic fibrosis patient: first case report from Malaysia

Authors: Vanitha Mariappan, Surendran Thavagnanam, Kumutha Malar Vellasamy, Cindy Ju Shuan Teh, Nadia Atiya, Sasheela Ponnampalavanar, Jamuna Vadivelu

Published in: BMC Infectious Diseases | Issue 1/2018

Login to get access

Abstract

Background

Burkholderia pseudomallei is the causative agent of melioidosis, which is a potentially life threatening disease endemic in Southeast Asian countries. In Malaysia, cystic fibrosis (CF) is an uncommon condition. The association between CF and B.pseudomallei infections has been reported previously. However, this is the first case report of a pediatric melioidosis relapse and co-infection with other Gram-negative bacteria in Malaysia.

Case presentation

A 14-year-old Chinese Malaysian boy presented with a history of recurrent pneumonia, poor growth and steatorrhoea since childhood, and was diagnosed with CF. B. pseudomallei was cultured from his sputum during three different admissions between 2013 and 2016. However, the patient succumbed to end stage of respiratory failure in 2017 despite antibiotics treatment against B.pseudomallei. The isolates were compared using multilocus-sequence typing and repetitive-element polymerase chain reaction (PCR), and confirmed that two of the isolates were of same sequence type, which may indicate relapse.

Conclusions

CF patients should be aware of melioidosis in endemic regions, as it is an emerging infectious disease, especially when persistent or recurrent respiratory symptoms and signs of infection occur. The high prevalence rates of melioidosis in Malaysia warrants better management options to improve quality of life, and life expectancy in patients with CF. Travel activities to endemic regions should also be given more consideration, as this would be crucial to identify and initiate appropriate empiric treatment.
Literature
2.
go back to reference Currie BJ, Dance DA, Cheng AC. The global distribution of Burkholderia pseudomallei and melioidosis: an update. Trans R Soc Trop Med Hyg. 2008;102(Suppl 1):S1–4.CrossRefPubMed Currie BJ, Dance DA, Cheng AC. The global distribution of Burkholderia pseudomallei and melioidosis: an update. Trans R Soc Trop Med Hyg. 2008;102(Suppl 1):S1–4.CrossRefPubMed
5.
go back to reference Rotz LD, Khan AS, Lillibridge SR, Ostroff SM, Hughes JM. Public health assessment of potential biological terrorism agents. Emerg Infect Dis. 2002;8:225–30.CrossRefPubMedPubMedCentral Rotz LD, Khan AS, Lillibridge SR, Ostroff SM, Hughes JM. Public health assessment of potential biological terrorism agents. Emerg Infect Dis. 2002;8:225–30.CrossRefPubMedPubMedCentral
7.
go back to reference Sanderson C, Currie BJ. Melioidosis: a pediatric disease. Pediatr Infect Dis J. 2014;33(7):770–1.CrossRefPubMed Sanderson C, Currie BJ. Melioidosis: a pediatric disease. Pediatr Infect Dis J. 2014;33(7):770–1.CrossRefPubMed
8.
go back to reference McLeod C, Morris PS, Bauert PA, Kilburn CJ, Ward LM, Baird RW, et al. Clinical presentation and medical management of melioidosis in children: a 24-year prospective study in the Northern Territory of Australia and review of the literature. Clin Infect Dis. 2015;60(1):21–6.CrossRefPubMed McLeod C, Morris PS, Bauert PA, Kilburn CJ, Ward LM, Baird RW, et al. Clinical presentation and medical management of melioidosis in children: a 24-year prospective study in the Northern Territory of Australia and review of the literature. Clin Infect Dis. 2015;60(1):21–6.CrossRefPubMed
9.
go back to reference Suppiah J, Thimma J, Cheah SH, Vadivelu J. Development and evaluation of polymerase chain reaction assay to detect Burkholderia genus and to differentiate the species in clinical specimens. FEMS Microbiol Lett. 2010;306:9–14.CrossRefPubMed Suppiah J, Thimma J, Cheah SH, Vadivelu J. Development and evaluation of polymerase chain reaction assay to detect Burkholderia genus and to differentiate the species in clinical specimens. FEMS Microbiol Lett. 2010;306:9–14.CrossRefPubMed
15.
go back to reference Asiah K, Hanifah YA, Norzila MZ, Hasniah L, Rusanida A. Unrecognised infection in a cystic fibrosis patient. J Paed Child Health. 2006;42:217–8.CrossRef Asiah K, Hanifah YA, Norzila MZ, Hasniah L, Rusanida A. Unrecognised infection in a cystic fibrosis patient. J Paed Child Health. 2006;42:217–8.CrossRef
16.
go back to reference Embi N, Suhaimi A, Mohamed R, Ismail G. Prevalence of antibodies to Pseudomonas pseudomallei exotoxin and whole cell antigens in military personnel in Sabah and Sarawak, Malaysia. Microbiol Immunol. 1992;36:899–904.CrossRefPubMed Embi N, Suhaimi A, Mohamed R, Ismail G. Prevalence of antibodies to Pseudomonas pseudomallei exotoxin and whole cell antigens in military personnel in Sabah and Sarawak, Malaysia. Microbiol Immunol. 1992;36:899–904.CrossRefPubMed
Metadata
Title
Relapse of chronic melioidosis in a paediatric cystic fibrosis patient: first case report from Malaysia
Authors
Vanitha Mariappan
Surendran Thavagnanam
Kumutha Malar Vellasamy
Cindy Ju Shuan Teh
Nadia Atiya
Sasheela Ponnampalavanar
Jamuna Vadivelu
Publication date
01-12-2018
Publisher
BioMed Central
Published in
BMC Infectious Diseases / Issue 1/2018
Electronic ISSN: 1471-2334
DOI
https://doi.org/10.1186/s12879-018-3371-7

Other articles of this Issue 1/2018

BMC Infectious Diseases 1/2018 Go to the issue