Gestational Trophoblastic Disease

Gestational Trophoblastic Disease
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Gestational Trophoblastic Disease (GTD) is a spectrum of proliferative abnormalities associated with pregnancy. It includes Hydatidiform Mole, Invasive Mole, Choriocarcinoma, and Placental site trophoblastic tumor (PSTT). The incidence varies across countries, with different types and etiologies contributing to its development. GTD is characterized by changes in chorionic villi, and factors such as maternal age, nutrition, and immune mechanisms play a role. Understanding the pathology, types, and etiology of GTD is essential in its management.

  • GTD
  • Trophoblastic Disease
  • Hydatidiform Mole
  • Pregnancy
  • Pathology

Uploaded on Feb 28, 2025 | 0 Views


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  1. GESTATIONAL TROPHOBLASTIC DISEASE

  2. DEFINITION Gestational Trophoblastic Disease(GTD) encompasses a spectrum of proliferative abnormalities of Trophoblastic associated with pregnancy Persistent GTD is referred as Gestational Trophoblastic Neoplasia(GTN)

  3. Conventional Histological Classification Hydatidiform Mole(Complete and partial) Invasive Mole Choriocarcinoma Placental site trophoblastic tumor(PSTT)

  4. HYDATIDIFORM MOLE

  5. DEFINITION It is an abnormal condition of the placenta where there are partly degenerative and partly proliferative changes in the young chorionic villi Cluster of small cyst Benign with malignant potential

  6. INCIDENCE Philippines 1 in 80 India 1 in 400 USA 1 in 2000

  7. TYPES COMPLETE INCOMPLETE

  8. ETIOLOGY Exact cause is unknown Highest in teenage pregnancies and women over 35 years of age Prevalence vary with race and ethnic origin Faulty nutrition

  9. ETIOLOGYContd Disturbed maternal immune mechanism Chromosomes are derived from the father H/O hydatidiform mole increase the chance of recurrence

  10. PATHOLOGY Disease of the CHORION Death of the ovum or Failure of the embryo to grow Hydatidiform mole (Cyst begin to form from 3rdto 5thweek, when feto-maternal circulation has become established)

  11. PATHOLOGY.Contd HYDATIDIFORM MOLE Secretions from hyperplastic cells and Transferred substances from the maternal blood Accumilation of these substances in the stroma of the villi(which are devoid of blood vessels) Distension of the villi to form small cyst

  12. NAKED EYE APPEARANCE Mass filling in the uterus Mass is made up of clusters of cyst of varying size No trace of embryo or amniotic sac

  13. MICROSCOPIC APPEARANCE Marked proliferation of syncitial and cyto- trophoblastic epithelium Thinning of stromal tissue due to accumulation of fluid Absence of blood vessels Villus pattern is distinctly maintained

  14. OVARIAN CHANGES Increased HCG Bilateral leuteal cyst (Increased HCG,P,E) Regress 2 months after expulsion of mole

  15. CLINICAL FEATURES AGE AND PARITY Prevalent amongst teenaged and elderly H/O amenorrhoea 8-12 weeks

  16. CLINICAL FEATURES..Contd SYMPTOMS Vaginal bleeding Varying degree of lower abdominal pain Over distension of the uterus Concealed haemorrhage Perforation of the uterus Infection Uterine contraction to expel the content

  17. CLINICAL FEATURES..Contd Constitutional symptoms Patient becomes sick Excessive vomiting Breathlessness Thyrotoxic feature Expulsion of grape like vesicles per vaginum is diagnostic H/O quickening absent

  18. CLINICAL FEATURES..Contd SIGNS Feature of early pregnancy Patient looks more ill Pallor out of proportion to visible blood loss Features of pre eclampsia

  19. CLINICAL FEATURES.Contd PER ABDOMEN Size of the uterus is more than the period of amenorrhoea Feel the uterus doughy Fetal parts are not felt No fetal movement Absence of FHS

  20. CLINICAL FEATURES.Contd VAGINAL EXAMINATION Internal ballottement cannot be elicited Unilateral or bilateral enlargement of the ovary Finding vesicles in the vaginal discharge Cervical os open

  21. INVESTIGATIONS Full blood count, ABO and Rh Hepatic, renal and thyroid function test Sonography Snow storm appearance HCG 1 in 200 to 1 in 500 X-Ray abdomen- No fetal shadow X-Ray chest Pulmonary embolism

  22. COMPLICATIONS Haemorrhage and shock Seperation Perforation Evacuation Infection No membranes Degenerated vesicles Lowered resistance Increased operative interference

  23. COMPLICATIONS..Contd Perforation of the uterus Dilatation and evacuation Perforating mole Pre eclampsia with convulsion Coagulation failure Acute pulmonary insufficiency 4-6 hours following evacuation LATE Choriocarcinoma

  24. MANAGEMENT PRINCIPLE 1. To restore the blood loss 2. To evacuate the uterus 3. To minimise infection

  25. MANAGEMENTContd PATIENT CLASSIFICATION GROUP A Mole is in the process of expulsion GROUP B Uterus remain inert

  26. MANAGEMENTContd SUPPORTIVE THERAPY GROUP A Morphine 15mg IM 5% Dextrose Blood transfusion GROUP B Blood should be kept ready prior to elective evacuation

  27. MANAGEMENTContd DEFINITIVE MANAGEMENT GROUP A S/E or D/E Oxytocin 10-20 units in 500 ml 5% dextrose 40-60 drops/minute Digital exploration and removal of ovum under GA using ovum forceps Methergin 0.2mg IM GROUP B Blood should be kept ready prior to elective evacuation Slow dialatation of the cervix followed by suction and evacuation

  28. COMPLICATIONS OF VAGINAL EVACUATION Injury to the uterus Haemorrhage Shock Acute pulmonary insufficiency Thyroid storm

  29. COMPLICATIONS OF VAGINAL EVACUATION Injury to the uterus Haemorrhage Shock Acute pulmonary insufficiency Thyroid storm

  30. INDICATIONS FOR HYSTERECTOMY Patient with age over 35yrs Completed family irrespective of age Uncontrolled haemorrhage or during surgical evacuation Reduces the risk of GTN

  31. INDICATIONS FOR HYSTEROTOMY Profuse vaginal bleeding Cervix unfavourable Accidental perforation of the uterus following surgical evacuation

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