Phellinus tropicalis abscesses in a patient with chronic granulomatous disease

Manish Ramesh1, Elena Resnick, Yiqun Hui

  • 1Departments of Medicine and Pediatrics, The Immunology Institute, Icahn School of Medicine at Mount Sinai, 1 Gustave L. Levy Place, Box 1089, New York, NY, 10029, USA.

Insights

Chronic Granulomatous Disease (CGD) patients face severe infections. A rare mold, Phellinus tropicalis, caused recurrent abscesses in a CGD patient, successfully treated with antifungal medication.

Area of Science:

  • Mycology
  • Immunology
  • Infectious Diseases

Background:

  • Chronic Granulomatous Disease (CGD) impairs the immune system, increasing susceptibility to life-threatening bacterial and fungal infections.
  • Genetic defects in the phagocyte NADPH oxidase pathway underlie CGD, complicating pathogen identification.

Observation:

  • A 24-year-old male with X-linked CGD presented with concurrent cervical and hip abscesses.
  • Initial cultures were non-diagnostic, and empirical antibiotic treatment failed, leading to abscess recurrence.
  • Microscopic examination revealed a filamentous organism, later identified as Phellinus tropicalis.

Findings:

  • Phellinus tropicalis (synonym: Inonotus tropicalis) was identified as the causative agent of recurrent abscesses in an immunocompromised CGD patient.
  • This represents the third reported human case of P. tropicalis infection, exclusively in individuals with CGD.
  • Antifungal treatment with voriconazole led to symptom resolution.

Implications:

  • Highlights Phellinus tropicalis as a potential pathogen in CGD patients, emphasizing the need for thorough microbiological investigation.
  • Underscores the importance of considering rare fungal pathogens in immunocompromised individuals with recurrent or refractory infections.
  • Suggests voriconazole as an effective treatment option for Phellinus tropicalis infections in CGD.

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