1 / 1

INTRODUCTION

INTRODUCTION. METHODOLOGY AND RESULTS. RESULTS. Gestational trophoblastic disease is a common gynaecological problem in Asia with incidence of 1 to 3 in 1000 pregnancies 2-7 . In Malaysia, the estimated incidence of molar pregnancy was 2.8 in 1000 deliveries in 1998 1 .

thu
Télécharger la présentation

INTRODUCTION

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. INTRODUCTION METHODOLOGY AND RESULTS RESULTS Gestational trophoblastic disease is a common gynaecological problem in Asia with incidence of 1 to 3 in 1000 pregnancies 2-7. In Malaysia, the estimated incidence of molar pregnancy was 2.8 in 1000 deliveries in 19981. GTD is considered highly curable, but accurate initial management is essential. GTD produces serum β-hCG level (human chorionic gonadotropin), which can be measured in either urine or serum and will be extremely high in molar pregnancy. After molar evacuation, patients should be followed with serum β-hCG level monitoring and are considered to have achieved remission when serum β-hCG level decline to undetectable level within six months. In view of possible theoretical risk of relapse or developing persistent gestational trophoblastic disease (pGTD), the patients are recommended for continued follow-up with serum β-hCG level for a period of two years. Women often defaulted follow-up and do not complete the recommended long protocol. The long protocol has caused significant practical and emotional complications to the woman and her family. DISCUSSION OBJECTIVES REFERENCES Sivanesaratnam V. The management of gestational trophoblastic disease in developing countries such as Malaysia. International Journal of Gynaecology & Obstetrics 1998. 60(1): 105-109. Ross SB, Donald PG. Current management of gestational trophoblastic diseases. Gynecologic Oncology. 2009; 112: 654 – 662. Mungan T, Kuscu E, Dabakoglu T et al. Hydatidiform mole: clinical analysis of 310 patients. Int J Gynecol Obstet. 1996; 52: 233-236. Dalya A, Tommaso B, George C et al. Recognising gestational trophoblastic disease. Best Practice & Research Clinical Obstetrics and Gynaecology. 2009; 23: 565-573. Soper JT, Mutch DG, Schink JC. American College of Obstetrician and Gynecologists. Diagnosis and treatment of gestational trophoblastic disease: ACOG Practice Bulletin No.53. Gynecol Oncol. 2004; 93(3): 575-585. Altieri A, Franceshi S, Ferlay et al. Epidemiology and aetiology of gestational trophoblastic diseases. Lancet Oncol. 2003; 4(11): 670-678. Audu BM, Takai IU, Chama CM et al. Hydatidiform mole as seen in a university teaching hospital: a 10-year review. J Obstet gynaecol. 2009; 29(4): 322-325. Hou JL, Wan XR, Xiang Y et al. Changes of clinical features in hydatidiform mole: analysis of 113 cases. J Reprod Med. 2008; 53(8): 629-633.

More Related