AI Article Synopsis

  • Bone marrow histology post-transplantation in patients with acute myelogenous leukemia (AML) was analyzed, focusing on differences between those with normal versus delayed recovery.
  • Of the 40 patients studied, the group with delayed recovery showed significant differences in bone marrow cellularity and reticulin structure, with some experiencing severe abnormalities and a notable case of hepatitis B infection mortality.
  • Findings suggest that bone marrow biopsies (BMB) are critical for understanding and investigating late engraftment issues, indicating that severe reticulin changes correlate with poor hematopoietic recovery.

Article Abstract

Bone marrow histology after bone marrow transplantation has rarely been studied. Here, we reviewed the pre- and post-transplant bone marrow biopsies (BMB) of 40 acute myelogenous leukemia (AML) patients autografted in our center, 28 with normal and 12 with delayed peripheral recovery. The two groups were comparable in terms of previous therapy, disease phase and the number of infused cells, and received the same conditioning regimen. In the former group, reduced bone marrow cellularity and mild reticulin abnormalities were usual histological findings; in the latter, five patients had the same pattern, but the other seven had an almost undetectable hematopoietic parenchyma and severe reticulin derangement. One of these seven patients died of reactivated hepatitis B virus infection; the others eventually achieved peripheral recovery, with none of them experiencing a relapse. Autografted AML patients are excellent subjects for histological investigations. They account for the majority of delayed engraftments, the contribution of extramedullary components to the timing of engraftment is minimal, and leukemia relapse cannot be ruled out. These results suggest that BMB is a useful investigation in the work-up of late engraftment. A high degree of reticulin derangement with an almost undetectable hematopoietic parenchyma appear to be the morphological hallmarks of late engraftment.

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Source
http://dx.doi.org/10.1038/sj.bmt.1702241DOI Listing

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