Histiocytic sarcoma (HS) is a malignant tumor composed of proliferating cells of histiocytic origin. True HS is exceedingly rare, particularly in pediatric patients. These tumors are frequently aggressive, and outcome for patients with HS has traditionally been poor. There is currently no consensus on the optimal management of these tumors, with the literature consisting largely of case reports and small case series utilizing a wide variety of therapies. We describe a case of HS in an 8-year-old female who was successfully treated with an abbreviated leukemia chemotherapy regimen.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/pbc.25100 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!