Toxoplasmosis after allogeneic stem cell transplantation--a single centre experience

Christoph Busemann1, Silvia Ribback, Kathrin Zimmermann

  • 1Department of Internal Medicine C (Haematology and Oncology, Marrow Transplantation), Ernst-Moritz-Arndt-University Greifswald, Ferdinand-Sauerbruch-Str, 17475, Greifswald, Germany.

Annals of Hematology
|January 18, 2012
PubMed

Insights

Toxoplasmosis is a serious complication after stem cell transplants. Real-time PCR shows higher sensitivity for diagnosing toxoplasmosis in transplant patients, suggesting improved monitoring and prophylaxis strategies.

Area of Science:

  • Medical Mycology
  • Infectious Diseases
  • Hematology

Background:

  • Toxoplasmosis is a rare but severe complication following allogeneic stem cell transplantation (SCT), often with a high mortality rate.
  • Current diagnostic methods, primarily imaging and molecular techniques, may have limitations in early detection.
  • Allogeneic SCT recipients are a vulnerable population susceptible to opportunistic infections.

Observation:

  • Three cases of toxoplasmosis in 155 allograft recipients at Greifswald University Hospital are presented.
  • Two cases of disseminated toxoplasmosis were diagnosed post-mortem in patients with multiple myeloma.
  • One patient with acute myeloid leukemia developed cerebral toxoplasmosis, confirmed by cerebrospinal fluid PCR.

Findings:

  • Conventional Toxoplasma gondii PCR showed limitations, with negative results in one case despite clinical suspicion.
  • Real-time PCR targeting a 529-bp genomic fragment demonstrated higher sensitivity in detecting Toxoplasma DNA compared to conventional PCR.
  • Toxoplasmosis was diagnosed late in the clinical course, highlighting diagnostic challenges.

Implications:

  • Rigorous real-time PCR monitoring is recommended for high-risk SCT patients or those with suspicious symptoms.
  • The findings suggest trimethoprim-sulfamethoxazole may be a preferred prophylaxis for Pneumocystis jirovecii pneumonia (PcP) over pentamidine in these patients.
  • Improved diagnostic sensitivity could lead to earlier treatment and potentially better outcomes for SCT recipients at risk of toxoplasmosis.