Pneumocystis jirovecii-induced chronic interstitial lung disease in Waldenström's macroglobulinemia

Wolfram Windisch1, Axel Meissner2, Axel Goßmann3

  • 1Kliniken der Stadt Köln gGmbH, Klinikum der Privaten Universität Witten/Herdecke, Lungenklinik, Ostmerheimer Str. 200, D-51109 Köln, Germany.

Future Microbiology
|March 14, 2017
PubMed

Insights

Pneumocystis jirovecii infections can exist in a spectrum from colonization to severe pneumonia. This case highlights a potential

Area of Science:

  • Pulmonology
  • Infectious Diseases
  • Critical Care Medicine

Background:

  • Pneumocystis jirovecii (PJP) is an opportunistic pathogen.
  • PJP infections range from asymptomatic colonization to life-threatening pneumonia.
  • A clinical "gray zone" between colonization and severe PJP pneumonia is often underestimated.

Observation:

  • A case of chronic interstitial lung disease and chronic cough was attributed to P. jirovecii.
  • The patient's chronic cough, potentially exacerbated by Waldenström's macroglobulinemia and ILD, was likely caused by P. jirovecii.

Findings:

  • Pneumocystis jirovecii infections may not always manifest as severe pneumonia.
  • This suggests a spectrum of PJP disease beyond simple colonization or critical illness.

Implications:

  • Serial testing is crucial for differentiating PJP colonization, "gray zone" infections, and early pneumonia.
  • This approach aids in appropriate patient management and treatment strategies.
  • Further research is needed to define the clinical significance of the PJP "gray zone".

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