AI Article Synopsis

  • Acute myeloid leukemia is rare in solid organ transplant recipients, often leading to relapse and infection.
  • A 4-year-old renal transplant patient presented with severe symptoms, including a high fever and gastritis, revealing esophageal masses upon examination.
  • Reducing immunosuppression resulted in a successful remission of the leukemia, highlighting the importance of early diagnosis and treatment in similar cases.

Article Abstract

Background: Acute myeloid leukemia after solid organ transplantation is a rare phenomenon. Few achieve remission; most succumb to relapse and infection.

Methods: A 4-year-old male renal transplant recipient on triple immunosuppression had culture-negative high spiking fever, persistent leukopenia, anemia and severe gastritis. Upper endoscopy showed 2 ulcerating masses in the lower esophagus.

Results: Esophageal biopsy showed a highly atypical myelo-monocytic infiltrate. A blastic population of cells featuring convoluted nuclear envelopes with an open chromatin pattern and abundant cytoplasm were filling the submucosa and infiltrating into the muscularis propria. Extensive investigation including bone marrow aspiration showed no spread. Drastic reduction of immunosuppression except 4-mg/d (0.22 mg/kg/d) prednisone for 2 to 3 weeks led to resolution of the leukemic process proven on repeat biopsy. The patient still is in remission 2 years later.

Conclusion: This case provides evidence that early diagnosis and aggressive reduction of immunosuppression may remit a posttransplant locally invasive acute myelo-monocytic infiltrative process.

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Source
http://dx.doi.org/10.1016/s0272-6386(03)00212-9DOI Listing

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