Background: Yolk sac tumors (YST) exhibit several different histologic
al subtypes and the mechanisms of cellular differentiation and prognos
is of each subtype remain unknown. Results: We report two infants with
sacrococcygeal YST; one represented a typical histological subtype an
d the other showed a hepatoid subtype with uniform histology. The isof
orm of alpha fetoprotein (AFP) in the patient with the hepatoid patter
n was examined by lectin-affinity immunoelectrophoresis and represente
d as a YST, but not hepatocellular, subtype. The patient with typical
YST responded well to VAB-6 combination chemotherapy. However, this re
gimen was only partially effective to the patient with the pure hepato
id histological subtype, and an etoposide with ifosfamide and cisplati
n (VIP) regimen as a salvage chemotherapy combined with complete tumor
resection was useful to achieve complete remission (CR). Both of the
patients have been in CR for more than four years.