z-logo
open-access-imgOpen Access
Heterotopic pregnancy after a spontaneous conception a case report with a review of clinical, laboratory and imaging findings
Author(s) -
Abdelmonem Ahmed H.,
Sayed Gamal,
Abugazia Abd Elwahid,
Kohla Samah,
Youssef Reda
Publication year - 2021
Publication title -
clinical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
ISSN - 2050-0904
DOI - 10.1002/ccr3.4649
Subject(s) - medicine , heterotopic pregnancy , pregnancy , magnetic resonance imaging , obstetrics and gynaecology , ectopic pregnancy , incidence (geometry) , obstetrics , spontaneous conception , first trimester , radiology , gestation , gestational sac , fertility , population , genetics , physics , environmental health , optics , biology
Heterotopic pregnancy (HP) describes the simultaneous presence of two pregnancies at different implantation sites. Usually, one pregnancy is intrauterine and the other one is ectopic. The incidence of HP after assisted reproductive technologies reaches 1:3900, but is very rare after a spontaneous pregnancy, with a reported incidence of 1 to 30,000 pregnancies. Due to its rarity, complex clinical picture, and laboratory findings, it is challenging to diagnose HP. We present a case of spontaneous HP diagnosed in the first trimester by ultrasound (US) and magnetic resonance imaging (MRI) and subsequently managed successfully. We present an analysis of the clinical and laboratory findings as well as imaging, including MRI that we used to diagnose the condition. Additionally, we performed a literature review. Conclusions HP is a very rare condition frequently faced in obstetrics, gynecology, and emergency departments that requires a high index of clinical suspicion. US remains the imaging modality of choice in diagnosing a HP, however, in some cases, an MRI with a reported safety in the first trimester, can be used to provide additional information over US.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here