Decidualised fallopian tube endometriotic implant causing spontaneous haemoperitoneum in a twin pregnancy
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چکیده
منابع مشابه
Endometriosis Nodule Causing Spontaneous Haemoperitoneum in Pregnancy: A Case Report and Literature Review
Spontaneous haemoperitoneum in pregnancy (SHiP) due to endometriosis is a very rare condition and this is a case of a 41-year-old primigravida, who presented at 32 weeks with sudden onset of severe lower abdominal pain without any uterine activity. This was a dichorionic-diamniotic twin pregnancy, following in vitro fertilisation for subfertility secondary to severe endometriosis. On admission,...
متن کاملA Molar Pregnancy within the Fallopian Tube
Background. Discussion of the incidence of molar pregnancy and ectopic pregnancy. Role of salpingostomy and special considerations for postoperative care. Case. The patient is a 29-year-old G7P4 who presented with vaginal bleeding in the first trimester and was initially thought to have a spontaneous abortion. Ultrasound was performed due to ongoing symptoms and an adnexal mass was noted. She u...
متن کاملIdiopathic spontaneous haemoperitoneum in the third trimester of pregnancy.
Spontaneous haemoperitoneum in pregnancy, more especially idiopathic ones are rare and can be life threatening. We present a case of a 30 year old pregnant woman who at 29 weeks gestation developed spontaneous haemoperitoneum. An exploratory laparotomy was done which did not reveal the source of the bleeding. She subsequently had conservative management as an inpatient until term when she had e...
متن کاملTwisted fallopian tube in pregnancy: a case report
BACKGROUND: Isolated twisted fallopian tube is an uncommon event, isolated twisted fallopian tube in pregnancy is also very rare. The diagnosis is often difficult and established during the operation. The right fallopian tube is most common affected. CASE PRESENTATION: We report an uncommon twisted left fallopian tube in pregnancy. A 34-year-old G3P2 28 weeks pregnant woman presented with acute...
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ژورنال
عنوان ژورنال: Case Reports
سال: 2014
ISSN: 1757-790X
DOI: 10.1136/bcr-2014-205317