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Vesicular Mole Dr. MOHAMMED ABDALLA EGYPT, DOMIAT G. HOSPITAL
It is a benign neoplasm of the chorionic villi
Incidence: 1:2000 pregnancies in United States and Europe 1:200 in Asia 10 times more in women over 45 years old. The increasing use of ultrasound in early pregnancy has probably led to the earlier diagnosis of molar pregnancy
1 -Maternal age : Young mothers (under age 20 years) have a slightly higher prevalence of GTD, although not nearly so great as those mothers over age 35 years.  2- Women who have had a previous molar gestation   3- The risk increases with the number of spontaneous  abortions . 4-  Women with blood type A  may be more likely to develop choriocarcinoma (but not hydatidiform mole);  RISK FACTORS:
What Is A Hydatidiform Mole? ,[object Object],It is the result of fertilisation of anucleated ovum  ( has no chromosomes)  with a sperm which will duplicate giving rise to  46 chromosomes of paternal origin only.  It is the result of fertilisation of an ovum by 2 sperms so the chromosomal number is  69 chromosomes   COMPLETE MOLE PARTIAL MOLE
Differentiation Between Complete And Partial Mole Rare 5-10% Malignant Changes Paternal and maternal 69 XXY or 69 XYY Paternal 46 XX (96%) or 46 XY (4%) Karyotype Focal Diffuse Trophoblastic hyperplasia Focal Diffuse Swelling of the villi Present Absent Embryonic or foetal tissue Partial Mole Complete Mole Feature
Three components make up the trophoblast: cytotrophoblast, syncytiotrophoblast intermediate trophoblast The cytotrophoblast is a stem cell with high mitotic activity but without hormonal synthesis. The syncytiotrophoblast, which constitutes the villous trophoblast, has low mitotic activity. The syncytiotrophoblast is responsible for the synthesis of the (beta-hCG) and can be identified with immunohistochemical stains. The intermediate trophoblast has features of the other two components and is responsible for endometrial invasion and implantation
[object Object],[object Object],Pathology microscopic evaluation  shows trophoblastic hyperplasia
[object Object],Pathology At histologic analysis ,  Uniformly edematous (hydropic) villi with dissolution of central stroma (cavitation/cistern
[object Object],Pathology At histologic analysis  Occasionally, necrosis is seen
[object Object],Pathology multiple theca lutein cysts in the ovaries in about 50% of cases.  exaggeration of the normal early pregnancy symptoms and signs
[object Object],[object Object],[object Object],[object Object],Pathology
Symptoms and Signs ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
GTD MOST COMMON: ,[object Object],[object Object],[object Object],[object Object],[object Object],LESS COMMON:
[object Object],Complete Hydatidiform Mole allows identification of numerous, discrete, anechoic  ( cystic )  spaces within a central area of heterogeneous echotexture
[object Object],Complete Hydatidiform Mole U/S evaluation .
Complete Hydatidiform Mole Theca lutein cysts multiloculated, often bilateral resolve after treatment of the intrauterine process Occasionally seen in twin gestations, fetal hydrops, pharmacologic stimulation (especially with human maternal gonadotropin) U/S evaluation .
[object Object],[object Object],Partial Hydatidiform Mole RCOG/ Fine C, Bundy A L, Berkowitz R S et al. Sonographic diagnosis of partial hydatidiform mole. Obstet Gynecol 1989;  73 :414-8.  Ultrasound has limited value in detecting partial molar pregnancies.  Grade C recommendations   U/S evaluation .
[object Object],(Grade C recommendation
twin pregnancies with a viable fetus and a molar pregnancy are associated with: reduced live birth rate of 25% risk from complications such as pre-eclampsia and haemorrhage. The subsequent need for chemotherapy, about 20%, is the same whether the pregnancy is terminated, or allowed to proceed to term.   */** ,[object Object],[object Object]
[object Object],Partial Hydatidiform Mole U/S evaluation .
[object Object],In twin pregnancy with a normal fetus and a coexistent complete mole maternal serum  AFP levels  are within the normal range. in partial molar pregnancy, elevated levels of AFP are found in the maternal serum and normal levels of AFP in the amniotic fluid Jauniaux E, Campbell S. Placenta and Cord. In: Dewbury K, Meire H, Cosgrove D, eds. Ultrasound in Obstetrics and Gynecology. London, United Kingdom. Churchill Livingstone 1993;448-9.  Freeman SB, Priest JH, Macmahon WC, Fernhoff PM, Elsas LJ. Prenatal ascertainment of triploidy by maternal serum alpha-fetoprotein screening. Prenat Diagn 1989;9:339-47.
RCOG Recommendations ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Grade C recommendation
Evacuation of Molar Pregnancies   ,[object Object],[object Object]
[object Object],Evacuation of Molar Pregnancies   ,[object Object]
[object Object],Evacuation of Molar Pregnancies   ,[object Object]
[object Object],[object Object],Gillespie A M, Tidy J, Bright N, Radstone C R, Coleman R E and Hancock B W. Primary gynaecological management of gestational trophoblastic tumours and the subsequent development of persistent trophoblastic disease. Br J Obstet Gynaecol 1998; 107(suppl 17) Abs. No. 287, p. 95.  Evacuation of Molar Pregnancies   Newlands E S. Presentation and management of persistent gestational trophoblastic disease and gestational trophoblastic tumours in the UK. In: Hancock B W, Newlands E S, Berkowitz R S, editors.  Gestational Trophoblastic Disease . London: Chapman and Hall 1997; 143-56.
Therapy: dilatation and suction curettage  ( at which time the diagnosis is confirmed ). 15% of women with complete hydatidiform mole will develop recurrent disease in the form of invasive mole or choriocarcinoma . all patients are followed up with successive serum beta - hCG measurements to allow early detection of persistent gestational trophoblastic neoplasia SO IF serial testing shows progressive decrease in the serum beta - hCG level The clinical diagnosis of complete hydatidiform mole is reached. Avoid pregnancy
At the Eleventh World Congress on Gestational Trophoblastic Disease 2001, over 70 cases of persistent low level hCG elevation were reported from four Trophoblast Centres. The majority view of an expert panel was to refrain from immediate chemotherapy and/or surgery but to monitor such patients carefully and repeatedly (even over many years) looking for evidence of tumour or for a definite rise in hCG values. Hancock BW, Everard JE, Drew D. Quiescent gestational trophoblastic disease (FTD): how common is it and what is its outcome? XIth World Congress on Gestational Trophoblastic Diseases, Santa Fe, 2001, abstract. Kohorn EI. Persistent low level hCG: a clinical enigma. XIth World Congress on Gestational Trophoblastic Disease, Santa Fe, 2001, abstract. Newlands ES, Seckl MJ, Foskett M, Short D, Fuller S and Mitchell H. Problems of interpretation of persistent low levels of hCG in patients suspected of having gestational trophoblastic disease (GTD). XIth World Congress on Gestational Trophoblastic Diseases, Santa Fe, 2001, abstract. Clinical management of persistent low level hCG elevation
[object Object],Evacuation of Molar Pregnancies   Bagshawe K D, Dent J, Webb J. Hydatidiform mole in England and Wales 1973-1983. Lancet 1986;  2 :673-7.
[object Object],[object Object],Evacuation of Molar Pregnancies   Newlands E S. Presentation and management of persistent gestational trophoblastic disease and gestational trophoblastic tumours in the UK. In: Hancock B W, Newlands E S, Berkowitz R S, editors.  Gestational Trophoblastic Disease . London: Chapman and Hall 1997; 143-56.
THANK YOU

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vesicular molle 2

  • 1. Vesicular Mole Dr. MOHAMMED ABDALLA EGYPT, DOMIAT G. HOSPITAL
  • 2. It is a benign neoplasm of the chorionic villi
  • 3. Incidence: 1:2000 pregnancies in United States and Europe 1:200 in Asia 10 times more in women over 45 years old. The increasing use of ultrasound in early pregnancy has probably led to the earlier diagnosis of molar pregnancy
  • 4. 1 -Maternal age : Young mothers (under age 20 years) have a slightly higher prevalence of GTD, although not nearly so great as those mothers over age 35 years. 2- Women who have had a previous molar gestation 3- The risk increases with the number of spontaneous abortions . 4- Women with blood type A may be more likely to develop choriocarcinoma (but not hydatidiform mole); RISK FACTORS:
  • 5.
  • 6. Differentiation Between Complete And Partial Mole Rare 5-10% Malignant Changes Paternal and maternal 69 XXY or 69 XYY Paternal 46 XX (96%) or 46 XY (4%) Karyotype Focal Diffuse Trophoblastic hyperplasia Focal Diffuse Swelling of the villi Present Absent Embryonic or foetal tissue Partial Mole Complete Mole Feature
  • 7. Three components make up the trophoblast: cytotrophoblast, syncytiotrophoblast intermediate trophoblast The cytotrophoblast is a stem cell with high mitotic activity but without hormonal synthesis. The syncytiotrophoblast, which constitutes the villous trophoblast, has low mitotic activity. The syncytiotrophoblast is responsible for the synthesis of the (beta-hCG) and can be identified with immunohistochemical stains. The intermediate trophoblast has features of the other two components and is responsible for endometrial invasion and implantation
  • 8.
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  • 17. Complete Hydatidiform Mole Theca lutein cysts multiloculated, often bilateral resolve after treatment of the intrauterine process Occasionally seen in twin gestations, fetal hydrops, pharmacologic stimulation (especially with human maternal gonadotropin) U/S evaluation .
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  • 27.
  • 28. Therapy: dilatation and suction curettage ( at which time the diagnosis is confirmed ). 15% of women with complete hydatidiform mole will develop recurrent disease in the form of invasive mole or choriocarcinoma . all patients are followed up with successive serum beta - hCG measurements to allow early detection of persistent gestational trophoblastic neoplasia SO IF serial testing shows progressive decrease in the serum beta - hCG level The clinical diagnosis of complete hydatidiform mole is reached. Avoid pregnancy
  • 29. At the Eleventh World Congress on Gestational Trophoblastic Disease 2001, over 70 cases of persistent low level hCG elevation were reported from four Trophoblast Centres. The majority view of an expert panel was to refrain from immediate chemotherapy and/or surgery but to monitor such patients carefully and repeatedly (even over many years) looking for evidence of tumour or for a definite rise in hCG values. Hancock BW, Everard JE, Drew D. Quiescent gestational trophoblastic disease (FTD): how common is it and what is its outcome? XIth World Congress on Gestational Trophoblastic Diseases, Santa Fe, 2001, abstract. Kohorn EI. Persistent low level hCG: a clinical enigma. XIth World Congress on Gestational Trophoblastic Disease, Santa Fe, 2001, abstract. Newlands ES, Seckl MJ, Foskett M, Short D, Fuller S and Mitchell H. Problems of interpretation of persistent low levels of hCG in patients suspected of having gestational trophoblastic disease (GTD). XIth World Congress on Gestational Trophoblastic Diseases, Santa Fe, 2001, abstract. Clinical management of persistent low level hCG elevation
  • 30.
  • 31.