Background. Hemolytic uremic syndrome (HUS) is an acquired disorder la
rgely affecting infants and young children. It is characterized by the
triad of microangiopathic hemolytic anemia, acute renal failure, and
thrombocytopenia. Although its etiology is unknown, viral and bacteria
l infections, disseminated malignancies in adults, and a variety of ch
emotherapeutic agents including cisplatin, have been implicated in its
occurrence. The association of HUS with chemotherapeutic agents after
its detection in a pediatric patient treated with cisplatin is review
ed. Methods. A 16-year-old male with osteosarcoma was treated with cis
platin as part of a chemotherapy protocol. After the fourth course, hi
s renal function deteriorated and necessitated cessation of cisplatin.
Nine months after the initiation of cisplatin, HUS developed. There w
as no evidence of residual tumor or metastatic disease. He received nu
merous packed erythrocyte and platelet transfusions for persistent hem
olysis and underwent several episodes of hemodialysis. Utilizing this
patient as an example, the authors reviewed the incidence of HUS devel
oping subsequent to the use of other chemotherapeutic agents. Results.
In the publishing literature, chemotherapy-associated HUS has been de
scribed to occur 54 days to 14 months after the initiation of chemothe
rapeutic regimens. A variety of agents was associated with the phenome
non. Conclusion. Hemolytic uremic syndrome may be a complication of ci
splatin, as evidenced by the condition that occurred in a 16-year-old
patient with osteosarcoma after cisplatin therapy.