Placental Site Trophoblastic Tumor: Clinical and Pathological Report of Two Cases
نویسندگان
چکیده مقاله:
Placental site trophoblastic tumor (PSTT) is the rare variant of gestational trophoblastic diseases (GTD), which differs histologically and immunologically from GTD. Diagnosis of PSTT is often difficult and delayed. In most cases, diagnosis is not possible until the surgery is performed. The most therapeutic choice is hysterectomy and it is usually successful. Here we report two cases of PSTT.
منابع مشابه
placental site trophoblastic tumor: clinical and pathological report of two cases
placental site trophoblastic tumor (pstt) is the rare variant of gestational trophoblastic diseases (gtd), which differs histologically and immunologically from gtd. diagnosis of pstt is often difficult and delayed. in most cases, diagnosis is not possible until the surgery is performed. the most therapeutic choice is hysterectomy and it is usually successful. here we report two cases of pstt.
متن کاملPlacental site trophoblastic tumor. Clinical and pathological report of two cases.
Placental site trophoblastic tumor (PSTT) is the rarest disease of the gestational trophoblast. Our two cases will be interesting not only because of the rarity of the disease, but because both were recognized before operation. Since the tumor cells are lined up tightly side by side, this disease must be distinguished primarily from tumors of epithelial origin. The authors highlight that the di...
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placental site trophoblastic tumor (pstt) is a very rare variant of gestational trophoblastic tumor. it can occur after normal termination of pregnancy or spontaneous abortion and ectopic or molar pregnancy. there is a wide range of clinical manifestations from a benign condition to an aggressive disease with fatal outcome. one of the most important characteristics of pstt, unlike other forms o...
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Placental site trophoblastic tumor is a very rare variant of gestational trophoblastic disease which differs histologically and immunocytochemically from gestational choriocarcinoma. The English language literature includes only 74 reported cases. Seventeen patients have been managed at Charing Cross Hospital with this diagnosis. The median follow-up is 4.6 years, and the 5-year overall surviva...
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عنوان ژورنال
دوره 5 شماره 2
صفحات 105- 108
تاریخ انتشار 2010-03-01
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