Gestational trophoblastic disease

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چکیده

estational trophoblastic disease includes following forms of growth disturbance of the human trophoblast: hydatiform mole, invasive mole, choriocarcinoma and placental site trophoblastic tumors. Term gestational trophoblastic disease is applied to the letter three conditions. Diagnosis and decision to institute treatment are sometimes undertaken without histopathological finding. Gestational trophoblastic disease is unique for its genetic origin, existence of ideal tumor marker bhCG and extremely high sensitivity to chemotherapy. This makes it curable in spite of its high malignant potential. Gestational trophoblastic disease appears as a result of abnormal gametogenesis and fertilization, so it represents natural neoplastic allograft with genetic material of another organism. Nongestational choriocarcinoma with primary ovarian or extragonadal localization also exists (1). Gestational trophoblastic disease can appear in any type of pregnancy. Hydatiform mole appears as a result of proliferation of cytotrophoblast and syncytiotrophoblast with different degrees of hyperplasia and dysplasia, hydropic degeneration of chorionic villi and disintegration of blood vessels. It appears as partial or complete. Disorders in partial mole are mild and focal. Karyotype is triploid, 69,XXY. Disorders of complete mole are severe in the absence of fetus or embryo. Genetic material derives from duplication of paternal haploid set (46,XX). In some cases it occurs as a result of dispermic fertilization of an empty egg (46,XY). Invasive mole (mole destruens, chorioadenoma destruens) has similar histological characteristics like a complete mole, but it is more aggressive, directly invades myometrium and its blood vessels, which often results in pulmonary embolisation. Distinction

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تاریخ انتشار 2002