2013
DOI: 10.1016/j.ejcdt.2013.02.002
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Microarray detection of fungal infection in pulmonary tuberculosis

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Cited by 21 publications
(21 citation statements)
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“…A. fumigatus was the dominant Aspergillus species detected in CPA patients followed by A. niger and A. flavus . Previous studies from Africa and Asia demonstrated the same distribution of Aspergillus species among TB patients, with A. fumigatus most common but with significant presence of A. niger and A. flavus [ 4 , 23 , 24 , 25 ]. This is different from the culture result of CPA patients from the UK, which was dominated by A. fumigatus (91%) [ 13 ].…”
Section: Discussionmentioning
confidence: 97%
“…A. fumigatus was the dominant Aspergillus species detected in CPA patients followed by A. niger and A. flavus . Previous studies from Africa and Asia demonstrated the same distribution of Aspergillus species among TB patients, with A. fumigatus most common but with significant presence of A. niger and A. flavus [ 4 , 23 , 24 , 25 ]. This is different from the culture result of CPA patients from the UK, which was dominated by A. fumigatus (91%) [ 13 ].…”
Section: Discussionmentioning
confidence: 97%
“…A. fumigatus, Aspergillus niger, H. capsulatum, C. neoformans and C. albicans are often responsible for causing severe secondary infections in tuberculosis patients. (10,56,58,59) Reactivation of latent cytomegalovirus (CMV) can lead to the development of concomitant or sequential fungal infections in immunosuppressed patients. Both solid organ and autologous stem cell transplant recipients, with a history of CMV infection, have higher risk for developing IFD.…”
Section: Invasive Candidiasismentioning
confidence: 99%
“…A. fumigatus , Aspergillus niger , H. capsulatum , C. neoformans and C. albicans are often responsible for causing severe secondary infections in tuberculosis patients. 10 , 56 , 58 , 59 …”
mentioning
confidence: 99%
“…The main risk factors of primary and secondary fungal pulmonary coinfection in TB patients include immunodeficiency due to mucosal or cutaneous barrier disruption, using broad-spectrum antibiotics and steroids, premature birth, hemodialysis, cytotoxic chemotherapy, tissue transplantation, chronic diseases, neutropenia, defects in the function of innate or cell-mediated immunity, metabolic syndrome, solid and hematologic malignancies, advanced age , recent radiation therapy, burns, prolonged hospitalization, severe trauma, bacterial infections, recent surgery, and implanted central intravascular access devices [7].…”
Section: Introductionmentioning
confidence: 99%