J. How et al., PLACENTAL SITE TROPHOBLASTIC TUMOR - REPORT OF 3 CASES AND REVIEW OF THE LITERATURE, International journal of gynecological cancer, 5(4), 1995, pp. 241-249
Three cases of placental site trophoblast tumor (PSTT) are added to 74
cases in the English language literature. One case presented with an
anorexic syndrome, the other two with amenorrhea and abnormal vaginal
bleeding. The three patients, whose lesions were confined to the uteru
s, were treated by total hysterectomy and their follow-up has been une
ventful. Review of the literature showed that 62 patients with PSTT we
re alive and 15 had died, two as a complication of treatment. The diag
nosis of PSTT may be difficult on a dilatation and currettage specimen
. Metastases are a powerful indicator of adverse outcome. Prognosis, a
s assessed on pathologic criteria, is unreliable; however, a mitotic c
ount of more than five mitoses per 10 high power fields is significant
. Surgery is the mainstay of treatment. Hysterectomy is generally indi
cated, but young patients who wish to remain fertile may be treated by
conservative surgery. In a few cases of progressive disease, chemothe
rapy has achieved remission, but generally chemotherapy and radiothera
py are ineffective. Long-term follow-up is essential as PSTT may progr
ess after years of remission. Serum human chorionic gonadotrophin (hCG
) levels are the best available marker of disease, but the disease may
still progress even if hCG levels are not raised.