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A case of pleural Mycobacterium tuberculosis infection with reversion of Quantiferon Gold Plus results from positive to negative.
Goire, N; Suchard, M S; Barling, A; Fernando, R; Dreyer, L; Mahony, A A.
Afiliación
  • Goire N; Microbiology Department, Australian Clinical Laboratories, Clayton, Victoria, Australia.
  • Suchard MS; University of Wollongong Faculty of Health and Behavioural Sciences: University of Wollongong, Wollongong, New South Wales, Australia.
  • Barling A; Microbiology Department, Australian Clinical Laboratories, Clayton, Victoria, Australia.
  • Fernando R; Chemical Pathology Department, School of Pathology, University of the Witwatersrand, Johannesburg, South Africa.
  • Dreyer L; Thoracic Surgery Department, Bendigo Hospital, Bendigo Health, Bendigo, Victoria, Australia.
  • Mahony AA; Histopathology Department, Australian Clinical Laboratories, Bendigo, Victoria, Australia.
Access Microbiol ; 6(9)2024.
Article en En | MEDLINE | ID: mdl-39239566
ABSTRACT
Introduction. Mycobacterium tuberculosis (MTB) infections continue to have a high mortality and morbidity burden globally. Interferon-gamma release assays such as Quantiferon Gold Plus (QFG-Plus) aid in diagnosis of latent TB but diagnosis of pleural TB remains challenging. We present a case of active pleural MTB infection with reversion from positive to negative of IGRA result as well as negative Xpert MTB/RIF Ultra PCR result from tissues obtained from pleural biopsy. Case summary. A 52-year-old otherwise healthy male presented in August 2022 with a 2 week history of pleuritic chest pain associated with modest elevation in inflammatory markers. The patient had had a positive QFG-Plus result in 2018, however QFG-Plus during this admission was negative. Computed-tomography pulmonary angiogram and needle thoracocentesis showed an exudative left pleural effusion with predominant lymphocytes. The patient's symptoms failed to resolve with empiric antimicrobial therapy for community-acquired pneumonia. Broncho-alveolar lavage as well as biopsies of pleural tissues via video-assisted thoracoscopic surgery from the left lower lobe yielded negative results on routine microbiological culture as well as Xpert Ultra PCR. Growth of acid-fast bacilli was noted from mycobacterial cultures of pleural tissues which was identified as MTB. Conclusion. Despite significant technological advances, microbiological diagnosis of MTB infections remains challenging. We document QFG-Plus reversion during development from latent to active pleural TB. Decline in the ability of CD4+ and CD8+ T cells to produce interferon gamma in response to TB antigens (ESAT-6 and CFP-10) was likely associated with loss of host control of latent MTB. This case serves as a reminder that despite exhaustive testing with state-of-art diagnostic platforms, MTB infections can still elude discovery.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Access Microbiol Año: 2024 Tipo del documento: Article País de afiliación: Australia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Access Microbiol Año: 2024 Tipo del documento: Article País de afiliación: Australia Pais de publicación: Reino Unido