Ectopic tubal pregnancy with partial mole: a rare case

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A very rare case of heterotopic pregnancy in natural conception with ectopic pregnancy as partial mole!

Heterotopic pregnancy is defined as the coexistence of intrauterine and extrauterine gestation. It was first reported in 1708 as an autopsy finding. The incidence was originally estimated on theoretical basis to be 1 in 30,000 pregnancies. However, more recent data indicate that the rate is higher because of assisted reproduction and is approximately 1 in 7,000 overall and as high as 1 in 900 w...

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Partial molar ectopic pregnancy: A case report

Partial or complete mole affects one in 1000  pregnancies.Partial mole is a rare form of ectopic pregnancy. There was a married woman,gravid 4,parity 1,abortion 1,and she had past medical history 0f right ectopic pregnancy.she had left ectopic pregnancy and was treated by laparascopic left salpyngectomy after failure of intramascular methotrexate treatment.After surgery  the pathology exam show...

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Hydatidiform mole presentation as a tubal ectopic pregnancy.

Presentation of hydatidiform mole as tubal ectopic pregnancy is very rare. These patients usually present with ectopic pregnancy and are later diagnosed with hydatidiform mole on the basis of histological examination following surgery. We present the case of a 32-year-old female who presented with abdominal pain and vaginal bleed since 2 days of presentation. She was vitally stable. There was m...

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Isolated torsion of a tubal ectopic pregnancy- a rare event.

Adnexal torsion accounts for 2.7% of all gynaecological emergencies, but isolated torsion of fallopian tube is an infrequent yet significant cause of lower abdominal pain in women, which generally presents in the reproductive age group. The overall incidence is 1 in 1.5 million women and is generally isolated and unilateral.(1) Patients typically present with intermittent pain related to torsio...

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ژورنال

عنوان ژورنال: International Journal of Reproduction, Contraception, Obstetrics and Gynecology

سال: 2018

ISSN: 2320-1789,2320-1770

DOI: 10.18203/2320-1770.ijrcog20181374