AI Article Synopsis

  • Rare invasive fungal infections are on the rise, especially in people with weakened immune systems, but diagnosing them is challenging due to their similar symptoms to more common infections.
  • A case is reported involving a young patient with Hodgkin lymphoma who died from a disseminated fungal infection, despite standard diagnostic methods detecting the pathogen.
  • The study highlights an experimental fungal PCR analysis that could speed up diagnosis and allow for faster treatment with targeted antifungal medications, potentially improving patient outcomes.

Article Abstract

Rare invasive fungal infections are increasingly emerging in hosts with predisposing factors such as immunodeficiency. Their timely diagnosis remains difficult, as their clinical picture may initially mimic infections with more common fungal species and species identification may be difficult with routine methods or may require time-consuming subcultures. This often results in ineffective drug administration and fatal outcomes. We report on a patient in their early twenties with mixed cellularity classical Hodgkin lymphoma with a disseminated () infection. Even though pathogen detection and identification was possible via the standard procedure consisting of culture followed by matrix-assisted laser desorption ionisation-time of flight (MALDI-TOF) mass spectrometry, the patient passed away in the course of multi organ failure. Herein, we report on a retrospectively applied experimental diagnostic fungal PCR-analysis used on an EDTA blood sample and consisting of two pan-fungal reactions and seven branch-specific reactions. Regarding invasive infection, this PCR array could considerably shorten time to diagnosis and switch to a targeted therapy with triazoles.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8749139PMC
http://dx.doi.org/10.1099/acmi.0.000285DOI Listing

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